Prof. FİRDEVS BAŞ

Publication Network

Articles 342

1. Use of serum MKRN3 and DLK1 levels in precocious puberty: association with an MKRN3 pathogenic variant.

Karakilic-Ozturan E., Karaman V., Gedikbaşı A., Poyrazoğlu Ş., Darendeliler F., Uyguner Z. O., et al.

Therapeutic advances in endocrinology and metabolism , vol.17, 2026 (SCI-Expanded, Scopus)

2. Transition of Care in X-Linked Hypophosphatemic Rickets: From Pediatric to Adult Practice- A Narrative Review.

Kandemir T., Bas F., Turan S., Öz Gül Ö., Kubat Uzum A.

Journal of clinical research in pediatric endocrinology , 2026 (SCI-Expanded, Scopus, TRDizin)

3. Hemodynamic and Microvascular Abnormalities in P450 Oxidoreductase Deficiency: Evidence for COX-Dependent Dysfunction.

Bayrak Demirel Ö., Yildiz M., Kucukgergin C., Karaman V., Kilinc S., Arik S. D., et al.

European journal of endocrinology , 2026 (SCI-Expanded, Scopus)

4. Molecular Diagnosis of 46,XY Disorders of Sex Development: An Efficient Initial Molecular Analysis Using a Custom-Designed Targeted Gene Panel in a Single-Center Study.

Poyrazoglu Ş., Aghayev A., Toksoy G., Karaman B., Aslanger A. D., Avci S., et al.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation , pp.1-16, 2026 (SCI-Expanded, Scopus)

5. Thyrotoxic Hypokalemic Periodic Paralysis Induced by High-Dose Insulin in an Adolescent Male with Type 1 Diabetes Mellitus.

Bayrak Demirel Ö., Koc C., Tercan U., Abali S., Kardelen A. D., Yildiz M., et al.

Hormone research in paediatrics , vol.99, no.1, pp.57-61, 2026 (SCI-Expanded, Scopus) Sustainable Development

6. Impact of Growth-promoting Therapies on Puberty, Growth, and Final Height in Classical 21-hydroxylase Deficiency

Yavaş Abali Z., Yildiz M., Abali S., Moniri A., Baş F., Onal H., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , 2025 (SCI-Expanded, Scopus)

7. Growth and pubertal development in children with familial Mediterranean fever under colchicine therapy

BAYRAK DEMİREL Ö., ARIK S. D., KANDEMİR T., AKGÜN Ö., KARDELEN AL A. D., YILDIZ M., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.185, no.1, 2025 (SCI-Expanded, Scopus)

8. Long-term follow-up of growth and puberty in 3-M syndrome: effects of growth hormone therapy and response variability

Ozturk A. P., Aslanger A. D., Altunoglu U., Gulec Ç., Karakilic Ozturan E., Karaman V., et al.

ENDOCRINE , vol.90, no.3, pp.1398-1411, 2025 (SCI-Expanded, Scopus)

9. The Outcome of Regular Well-Child Follow-Up From Birth on Adolescent Well-Being.

Aksakal M. Z., Aşkan Ö. Ö., Kayı A. B., Şahin A. Y., Keskindemirci G., Kuleli O., et al.

Child: care, health and development , vol.51, no.6, 2025 (SCI-Expanded, SSCI, Scopus)

10. Impact of parental fear of hypoglycemia on quality of life in children with type 1 diabetes and their parents

Yildiz M., KOÇ ÇALIŞGAN C., Karaca N., Toparlak D., Yanik H., Kandemir T., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.98, pp.411-412, 2025 (SCI-Expanded, Scopus)

11. Type 1 Diabetes Mellitus and Transfer from Pediatric to Adult Care: A Single-Center Experience.

Yiğit Yalçın B., Tercan U., Yildiz M., Hacısahinogulları H., Yenidünya Yalın G., Gül N., et al.

Journal of clinical research in pediatric endocrinology , 2025 (SCI-Expanded, Scopus, TRDizin)

12. **Clinical and Genetic Mechanisms in Patients with MC2R Deficiency Presenting with Early Puberty**

Karakilic Ozturan E., Yavas Abali Z., Karaman V., Poyrazoglu Ş., Uyguner Z. O., Darendeliler F., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.98, no.5, pp.543-550, 2025 (SCI-Expanded, Scopus) Sustainable Development

13. Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinism.

Yavas Abali Z., BAŞ F., Houghton J. A. L., ABALI S., Karakilic Ozturan E., Gulec Ç., et al.

Endocrine , vol.89, no.2, pp.416-428, 2025 (SCI-Expanded, Scopus) Sustainable Development

14. Young Turkish Adults Show a Continuing Positive Secular Change of Height But an Alarming Increase of Overweight in Males: Pilot Study for the Initiation of Updated Growth Charts.

Bayrak Demirel Ö., Koç C., Şükür N. M., Kardelen Al A. D., Yildiz M., Poyrazoğlu Ş., et al.

Journal of clinical research in pediatric endocrinology , 2025 (SCI-Expanded, Scopus, TRDizin)

15. Exploring the Heterogeneity of Pediatric Neuroendocrine Tumors: Single-Center Experience.

Koc C., Yola Atalah Y. E., Bayrakoglu S., Yildiz M., Onder S., Yegen G., et al.

Hormone research in paediatrics , pp.1-8, 2025 (SCI-Expanded, Scopus)

16. Pubertal development in hypophosphatemic rickets: does it have an impact on growth?

Kandemir T., Bayrak Demirel Ö., Koç Çalışgan C., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

Endocrine , no.volume 110, pp.217-218, 2025 (Peer-Reviewed Journal)

17. Expanding the Clinical and Mutational Spectrum of Biallelic POC1A Variants: Characterization of Four Patients and a Comprehensive Review of POC1A-Related Phenotypes.

Altunoglu U., Turgut G. T., Özturan E. K., Kalaycı T., Kaya M., TOKSOY G., et al.

Clinical genetics , vol.107, no.4, pp.390-401, 2025 (SCI-Expanded, Scopus)

18. A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings

Yildiz M., Onal Z., Yesil G., Kabil T. G., Toksoy G., Poyrazoglu Ş., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.17, no.1, pp.97-102, 2025 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

19. Investigation of dysmenorrhea in adolescent girls with familial Mediterranean fever: a comparative study with healthy controls

DEMİRKAN F. G., Yetim Şahin A., Çakmak F., Akgün Ö., Guliyeva V., Tuğrul Aksakal M. Z., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.184, no.3, 2025 (SCI-Expanded, Scopus)

20. Cabergoline Induced Pathological Gambling in an Adolescent with Prolactinoma.

Tercan U., Sarban E., Yildiz M., Erbasi O. N., Ozkan M., Kardelen A. D., et al.

Journal of clinical research in pediatric endocrinology , 2025 (SCI-Expanded, Scopus, TRDizin)

21. Central Adrenal Insufficiency: Etiology and Diagnostic Approach

Yıldız M., Yıldırım R., BAŞ F.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.17, pp.72-79, 2025 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

22. Serum Vitamin D Levels in Asthmatic Children and Adolescents and Its Relationship with Asthma Control

Murat N. O., BAŞ F., Mutlu U., Guler N., ALTINEL Z. Ü.

JOURNAL OF CHILD - COCUK DERGISI , vol.25, no.4, pp.246-251, 2025 (ESCI, TRDizin)

23. Olfactory Receptor Gene Deletions: A Novel Genetic Findings in Idiopathic Prepubertal Gynecomastia and Juvenile Macromastia.

Bas F., Karaman B., Kardelen A. D., Heidargholizadeh S., Najafli A., Toksoy G., et al.

Hormone research in paediatrics , pp.1-9, 2025 (SCI-Expanded, Scopus)

24. Small Head Circumference and Height above Target Height as Potential Early Clues for Klinefelter Syndrome: A Retrospective Cohort Study

Kardelen Al A. D., Oner D. O., Demirel O. B., Şükür N. M., Yıldız M., Poyrazoğlu Ş., et al.

JOURNAL OF CHILD - COCUK DERGISI , vol.25, no.4, pp.285-289, 2025 (ESCI, TRDizin)

25. The Relationship Between Sleep Quality, Sleep Duration, Social Jet Lag and Obesity in Adolescents.

Yıldız F., Tuğrul Aksakal M. Z., Yıldız R., Baş F.

Journal of clinical research in pediatric endocrinology , vol.16, no.4, pp.419-425, 2024 (SCI-Expanded, Scopus, TRDizin)

26. Evaluation of the ability of insulin resistance and lipid-related indices to predict the presence of NAFLD in obese adolescents

Yetim A., Şahin M., Kandemir İ., Bulakçı B., Aksakal M. Z., Karapınar E., et al.

LIPIDS IN HEALTH AND DISEASE , vol.23, no.1, 2024 (SCI-Expanded, Scopus) Sustainable Development

27. A Rare Coexistence of Turner Syndrome and Mycosis Fungoides: A Case Report.

Bayrak Demirel Ö., Karakilic-Ozturan E., Atci T., Ozturk Sari Ş., Baykal C., Kardelen Al A. D., et al.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded, Scopus, TRDizin)

28. Effect of obesity and NAFLD on leukocyte telomere length and hTERT gene MNS16A VNTR variant.

Kandemir I., Sahin A. Y., Oyaci Y., Khudiyeva S., Sahin M., Aksakal M. Z., et al.

Scientific reports , vol.14, no.1, pp.25055, 2024 (SCI-Expanded, Scopus) Sustainable Development

29. Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the Literature.

Kandemir T., Karakilic Ozturan E., Dural Ö., Aslanger A. D., İnan Balcı E., Bayram A., et al.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded, Scopus, TRDizin)

30. Evaluation of microvascular abnormalities and metabolic status in children with non-syndromic early-onset severe obesity using nailfold capillaroscopy

TERCAN U., AKGÜN Ö., KANDEMİR T., KARDELEN AL A. D., YILDIZ M., POYRAZOĞLU Ş., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.97, pp.230-231, 2024 (SCI-Expanded, Scopus)

31. Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship

Özsu E., Çetinkaya S., Bolu S., Hatipoğlu N., Savaş Erdeve Ş., Evliyaoğlu S. O., et al.

Journal of clinical research in pediatric endocrinology , vol.16, no.3, pp.297-305, 2024 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

32. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

ŞIKLAR Z., ÇAMTOSUN E., Bolu S., YILDIZ M., Akinci A., BAŞ F., et al.

ENDOCRINE , vol.85, pp.1407-1416, 2024 (SCI-Expanded, Scopus)

33. Association of problems, coping styles, and preferred online activity with depression, anxiety, and other psychological disorders in Turkish adolescents diagnosed with chronic kidney disease

Kandemir I., Gudek K., Sahin A., Aksakal M. Z., Kucuk E., Yildirim Z. N. Y., et al.

PEDIATRIC NEPHROLOGY , vol.39, no.9, pp.2779-2788, 2024 (SCI-Expanded, Scopus)

34. Novel variants ensued genomic imprinting in familial central precocious puberty

Karaman V., Karakilic-Ozturan E., Poyrazoglu Ş., Gelmez M. Y., Bas F., Darendeliler F., et al.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.47, no.8, pp.2041-2052, 2024 (SCI-Expanded, Scopus)

35. Assessing Psychological Disorders in Turkish Adolescents with Transfusion-Dependent Thalassemia

Yetim Şahin A., Kandemir I., Dağ H., Türkkan E., Aksakal M. T., Sahin M., et al.

CHILDREN (BASEL) , vol.11, no.2, pp.837-839, 2024 (SCI-Expanded, Scopus)

36. The Effects of the COVID-19 Pandemic on Pubertal Development in Girls: A Retrospective Evaluation of Girls Presenting with Precocious Puberty Before and During the Pandemic

Ozturan E. K., Ozden A. B. A., KANDEMİR T., POYRAZOĞLU Ş., BAŞ F., Darendeliler F.

JOURNAL OF CHILD - COCUK DERGISI , no.4, pp.215-218, 2024 (ESCI, TRDizin) Sustainable Development

37. SPIOMET4HEALTH—efficacy, tolerability and safety of lifestyle intervention plus a fixed dose combination of spironolactone, pioglitazone and metformin (SPIOMET) for adolescent girls and young women with polycystic ovary syndrome: study protocol for a multicentre, randomised, double-blind, placebo-controlled, four-arm, parallel-group, phase II clinical trial

Garcia-Beltran C., Malpique R., Andersen M. S., Baş F., Bassols J., Darendeliler F., et al.

Trials , vol.24, no.1, 2023 (SCI-Expanded, Scopus)

38. In response to: “Letter to: Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey”.

Karakılıç Özturan E., Öztürk A. P., Baş F., Erdoğdu A. B., Kaptan S., Kardelen Al A. D., et al.

Journal of clinical research in pediatric endocrinology , vol.15, no.4, pp.451-452, 2023 (SCI-Expanded, Scopus, TRDizin)

39. Effects of Growth Hormone Therapy on Glucose Metabolism in Children and Adolescents: 1-year follow-up results

KARDELEN AL A. D., KANDEMİR T., Demirel O., TERCAN U., YILDIZ M., POYRAZOĞLU Ş., et al.

HORMONE RESEARCH IN PAEDIATRICS , pp.280, 2023 (SCI-Expanded, Scopus)

40. Obesity and Insulin Resistance in Patients with Achondroplasia

İNAN BALCI E., KARDELEN AL A. D., BAŞ F., YILDIZ M., POYRAZOĞLU Ş., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , pp.172-173, 2023 (SCI-Expanded, Scopus) Sustainable Development

41. A Rare Diagnosis in a Virilized Adolescent with a 46,XX Karyotype: Gonadoblastoma with Dysgerminoma

KANDEMİR T., Ozturan E. K., DURAL Ö., ASLANGER A. D., İNAN BALCI E., BAYRAM A., et al.

HORMONE RESEARCH IN PAEDIATRICS , pp.559, 2023 (SCI-Expanded, Scopus)

42. Evaluation of Serum MKRN3 and DLK1 Concentrations for Predicting Variant Detection in MKRN3 and DLK1Genes in Patients with Central Precocious Puberty

Ozturan E. K., Karaman V., Gedikbaşı A., Poyrazoğlu Ş., Uyguner Z. O., Darendeliler F., et al.

HORMONE RESEARCH IN PAEDIATRICS , pp.97-98, 2023 (SCI-Expanded, Scopus)

43. A Rare Coexistence of Turner Syndrome and Mycosis Fungoides: A Case Report

Demirel O. B., Ozturan E. K., KARDELEN AL A. D., YILDIZ M., POYRAZOĞLU Ş., BAŞ F., et al.

HORMONE RESEARCH IN PAEDIATRICS , pp.309-310, 2023 (SCI-Expanded, Scopus)

44. Motivational Interviewing Techniques for an Obese Adolescent: A Case Report and Literature Review

YETİM ŞAHİN A., ELİUZ TİPİCİ B., Durak C., Apaydin R., Gudek K., BAŞ F.

JOURNAL OF CHILD - COCUK DERGISI , vol.23, no.2, pp.189-193, 2023 (ESCI, TRDizin) Sustainable Development

45. A novel RNPC3 gene variant expands the phenotype in patients with congenital hypopituitarism and neuropathy

Abali Z. Y., Ili E. G., Baş F., Ozkan M. U., Güleç Ç., Toksoy G., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.97, no.2, pp.157-164, 2023 (SCI-Expanded, Scopus) Sustainable Development

46. Phenotype-genotype correlations of GH1 gene variants in patients with isolated growth hormone deficiency (IGHD) or multiple pituitary hormone deficiency (MPHD)

Öztürk A. P., Abali Z. Y., Aslanger A. D., Baş F., Toksoy G., Karaman V., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.97, no.2, pp.126-133, 2023 (SCI-Expanded, Scopus) Sustainable Development

47. Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A SingleCenter Experience.

Yavaş Abalı Z., Öztürk A. P., BAŞ F., Poyrazoğlu Ş., Akcan N., KEBUDİ R., et al.

Turkish archives of pediatrics , vol.58, no.3, pp.308-313, 2023 (ESCI, TRDizin) Sustainable Development

48. PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency

Kardelen A. D., Najafli A., Baş F., Karaman B., Toksoy G., Poyrazoğlu Ş., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.15, no.4, pp.338-347, 2023 (SCI-Expanded, Scopus, TRDizin)

49. A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care

Kardelen A. D., Karakılıç Özturan E., Poyrazoğlu Ş., Baş F., Ceylaner S., Joustra S. D., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.15, no.4, pp.431-437, 2023 (SCI-Expanded, Scopus, TRDizin)

50. THE INFLUENCE OF GROWTH HORMONE TREATMENT ON INSULIN SENSITIVITY IN CHILDREN AND ADOLESCENTS

KARDELEN AL A. D., KARAKILIÇ ÖZTURAN E., KANDEMİR T., BAYRAK DEMİREL Ö., TERCAN U., ARSLAN S., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.86, no.4, pp.275-281, 2023 (ESCI, TRDizin) Sustainable Development

51. Evaluation of Children with Secondary Osteoporosis: A Single-center Experience

Abalı Z. Y., BAŞ F., Poyrazoğlu Ş., Öztürk A. P., Bundak R., Darendeliler F.

MEDICAL JOURNAL OF BAKIRKOY , vol.19, no.1, pp.51-56, 2023 (ESCI, Scopus)

52. Body proportions in patients with Turner syndrome on growth hormone treatment

Kardelen A. D., Şükür M., Özturan E. K., Öztürk A. P., Poyrazoğlu Ş., BAŞ F., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , vol.53, no.2, pp.518-525, 2023 (SCI-Expanded, Scopus, TRDizin)

53. COURSE OF PAPILLARY THYROID CARCINOMA DIAGNOSED IN CHILDHOOD AND ADOLESCENCE AND FOLLOWED THROUGH ADULTHOOD: EXPERIENCE FROM A TERTIARY REFERRAL CENTER

Haci̇Şahi̇Noğullari H., Balci E. İ., İŞCAN A. Y., Yalin G., Selcukbiricik Ö. S., SORMAZ İ. C., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.86, no.4, pp.282-287, 2023 (ESCI, TRDizin) Sustainable Development

54. Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone

Saygili S., Kocaaga M., Kaya G., Sukur M., Bas F., Poyrazoglu Ş., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.15, no.1, pp.69-80, 2023 (SCI-Expanded, Scopus, TRDizin)

55. Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey

Karakilic Ozturan E., Ozturk A. P., Bas F., Erdogdu A. B., Kaptan S., Kardelen Al A. D., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.15, no.3, pp.276-284, 2023 (SCI-Expanded, Scopus, TRDizin)

56. Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

Aycan Z., Keskin M., Lafci N. G., Savas-Erdeve S., Baş F., Poyrazoğlu Ş., et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.65, no.12, 2022 (SCI-Expanded, Scopus)

57. **Investigation of Genes Associated with Multiple Pituitary Hormone Deficiencies via Next Generation Sequencing Technology**

ÖZTÜRK A. P., TOKSOY G., BAŞ F., Abali Z. Y., Bagirova G., KARAMAN V., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.91-92, 2022 (SCI-Expanded, Scopus)

58. Papillary Tyhroid Carcinoma in Two Siblings With Congenital Famial Hypothyroidism

Balci E. I., Yilmaz M., Poyrazoglu Ş., Bas F., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.571-572, 2022 (SCI-Expanded, Scopus)

59. A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels

Ozturan E. K., Karaman V., Gelmez M. Y., Yildiz M., Poyrazoglu Ş., Bas F., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.351, 2022 (SCI-Expanded, Scopus)

60. Evaluation of Early Puberty in Patients with MC2R Deficiency

Ozturan E. K., Bas F., Abali Z. Y., Karaman V., Poyrazoglu Ş., Uyguner Z. O., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.354, 2022 (SCI-Expanded, Scopus)

61. Evaluation of Genetic Etiology in Children Born Small for Gestational Age with Persistent Short Stature: Preliminary Results

Ozturk A. P., Aslanger A., Ozturan E. K., Konur E. N., Gulec C., Karaman V., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.313, 2022 (SCI-Expanded, Scopus)

62. Gender Dysphoria in Adolescents

DAĞ H., BAŞ F.

Çocuk Dergisi , vol.22, no.2, pp.124-130, 2022 (TRDizin)

63. Adolesan Çağındaki Çocuklarda Otoimmün Tiroiditte Parvovirus B19'un Rolü

DURAK C., YAVAŞ ABALI Z., KÖKSAL M. O., BEKA H., AĞAÇFİDAN A., OĞUZ F., et al.

Online Türk Sağlık Bilimleri Dergisi , vol.7, no.3, pp.493-498, 2022 (TRDizin)

64. Growth and Pubertal Features in a Cohort of 83 Patients with Osteogenesis Imperfecta.

Ozturk A. P., Dudakli A., Ozturan E., Poyrazoglu Ş., Bas F., Darendeliler F.

Klinische Padiatrie , vol.234, no.4, pp.199-205, 2022 (SCI-Expanded, Scopus) Sustainable Development

65. Ovarian and paraovarian adrenal rest tumors are not uncommon in gonadectomy materials of historical congenital adrenal hyperplasia cases in childhood

Yildiz M., Bayram A., BAŞ F., Karaman V., TOKSOY G., Poyrazoglu Ş., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.187, no.1, 2022 (SCI-Expanded, Scopus)

66. SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS

Karakilic-Ozturan E., ÖZTÜRK A., ÖNEY C., KARDELEN AL A. D., YÜRÜK YILDIRIM Z. N., BALCI H. İ., et al.

ACTA ENDOCRINOLOGICA-BUCHAREST , vol.18, no.3, pp.387-391, 2022 (SCI-Expanded, Scopus) Sustainable Development

67. Evaluation of growth, puberty, osteoporosis, and the response to long-term bisphosphonate therapy in four patients with osteoporosis-pseudoglioma syndrome

Karakilic-Ozturan E., Altunoglu U., Ozturk A. P., Kardelen Al A. D., Yavas Abali Z., Avci S., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.188, no.7, pp.2061-2070, 2022 (SCI-Expanded, Scopus)

68. Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.

Akcan N., Uyguner Z. O., Bas F., Altunoglu U., Toksoy G., Karaman B., et al.

Journal of clinical research in pediatric endocrinology , vol.14, no.2, pp.153-171, 2022 (SCI-Expanded, Scopus, TRDizin)

69. Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD

Akcan N., Uyguner O., Bas F., Altunoglu U., Toksoy G., Karaman B., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.14, no.2, pp.153-171, 2022 (SCI-Expanded, Scopus, TRDizin)

70. Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards

Bundak R., Abali Z. Y., Furman A., Darendeliler F., Gokcay G., Bas F., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.14, no.2, pp.207-215, 2022 (SCI-Expanded, Scopus, TRDizin)

71. Impact of Smoking, Obesity and Maternal Diabetes on SHBG Levels in Newborns.

Aydin B. K., Yasa B., Moore J. P., Yasa C., Poyrazoglu Ş., Bas F., et al.

Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association , vol.130, no.5, pp.335-342, 2022 (SCI-Expanded, Scopus) Sustainable Development

72. Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report

Hatun S., DALGIÇ B., Goksen D., Aydogdu S., Erdeve S. S., Kulogu Z., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , no.1, pp.1-9, 2022 (SCI-Expanded, Scopus, TRDizin)

73. Pelvic and breast ultrasound abnormalities and associated metabolic disturbances in girls with premature pubarche due to adrenarche.

Aydin B. K., Kadioglu A., Kaya G. A., Devecioglu E., Baş F., Poyrazoğlu Ş., et al.

Clinical endocrinology , vol.96, no.3, pp.339-345, 2022 (SCI-Expanded, Scopus) Sustainable Development

74. BONE HEALTH AND GROWTH IN SPINAL MUSCULAR ATROPHY TYPE 2 AND 3

Kipoglu O., Ozturan E. K., Coskun O., Ozturk A. P., Yildiz E. P., Bas F., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.85, no.1, pp.22-28, 2022 (ESCI, TRDizin)

75. Long-term Follow-up of a Toddler with Papillary Thyroid Carcinoma: A Case Report with a Literature Review of Patients Under 5 Years of Age

Öztürk A. P., Karakılıç Özturan E., Gün Soysal F., Ünal S., Işık G., Yegen G., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.14, no.1, pp.119-125, 2022 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

76. COMPARISON OF SINGLE DOSE AND MULTI-DOSE hCG STIMULATION TESTS

Kardelen A. D., Ozturan E. K., Asgarova L., Ozturk A. P., Yildiz M., Poyrazoglu Ş., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.85, no.2, pp.223-227, 2022 (ESCI, TRDizin)

77. Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C.

ÇİÇEK D., Warr N., Yesil G., Eker H. K., Bas F., Poyrazoglu Ş., et al.

European journal of endocrinology , vol.186, no.1, pp.65-72, 2021 (SCI-Expanded, Scopus)

78. Evaluation of the Efficacy and Safety of 3 Different Management Protocols in Pediatric Diabetic Ketoacidosis.

Akcan N., Uysalol M., Kandemir I., Soydemir D., Abali Z., Poyrazoglu Ş., et al.

Pediatric emergency care , vol.37, 2021 (SCI-Expanded, Scopus)

79. The relationship between urinary bisphenol A levels and body weight in children Bisphenol A levels and body weight

KILIÇ A., GÜMÜŞ PEKACAR S., YETİM ŞAHİN A., KESKİNDEMİRCİ G., ÖZÇETİN M., VARKAL M. A., et al.

ANNALS OF CLINICAL AND ANALYTICAL MEDICINE , no.11, pp.1239-1243, 2021 (ESCI) Sustainable Development

80. Evaluation of Persistent Short Stature in Children Born Small for Gestational Age without Catch-up Growth

Ozturk A. P., Ozturan K., Poyrazoglu Ş., Bas F., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.136, 2021 (SCI-Expanded, Scopus)

81. Response to growth hormone therapy with high IGF-1-levels and severe insulin resistance in two-cases with SOFT syndrome: A novel homozygous mutation in POC1A

Karakilic-Ozturan E., Altuoglu U., Ozturk A. P., Toksoy G., Turgut G. T., Poyrazoglu Ş., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.317, 2021 (SCI-Expanded, Scopus)

82. **Biallelic PPP2R3C mutations are associated with partial and complete gonadal dysgenesis in 46,XY and 46,XX individuals**

ÇİÇEK D., Warr N., Yesil G., Eker H. K., Bas F., Poyrazoglu Ş., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.92, 2021 (SCI-Expanded, Scopus)

83. Growth and Puberty in Patients with Osteogenesis Imperfecta

Ozturk A. P., Ozturan E. K., Poyrazoglu Ş., Bas F., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.94-95, 2021 (SCI-Expanded, Scopus)

84. Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11 beta-Hydroxylase Deficiency

Yildiz M., Isik E., Abali Z. Y., Keskin M., Ozbek M. N., Bas F., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.106, no.9, 2021 (SCI-Expanded, Scopus)

85. Sequence of MKRN3 and DLK1 genes in cases with familial central precocious puberty

Karaman V., Karakilic-Ozturan E., Bas F., Poyrazoglu Ş., Basaran S., Darendeliler F., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.167-168, 2021 (SCI-Expanded, Scopus)

86. Effects of growth hormone therapy on serum concentrations of IGF-1 in patients with Turner syndrome: High IGF-1 concentrations despite optimal dose?

Ozturan E. K., Karagoz N., Ceylaner S., Ozturk A. P., Al A. D. K., Abali Z. Y., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.317-318, 2021 (SCI-Expanded, Scopus)

87. Phenotypic Characteristics of Patients with 45,X/46,XY Mosaicism: Growth, Gonadal Pathology and Tumour Risk

Poyrazoglu Ş., Bas F., Karaman B., Yildiz M., Basaran S., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.86-87, 2021 (SCI-Expanded, Scopus)

88. Evaluation of early puberty in boys and girls with Silver-Russell Syndrome: Discordance between testicular growth and pituitary-gonadal hormones in male cases

Yildiz M., Bas F., Karaman B., Poyrazoglu Ş., Basaran S., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.135-136, 2021 (SCI-Expanded, Scopus)

89. Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

Savaş-Erdeve Ş., Aycan Z., Çetinkaya S., Ozturk A. P., Bas F., Poyrazoglu Ş., et al.

Journal of clinical research in pediatric endocrinology , vol.13, no.2, pp.180-186, 2021 (SCI-Expanded, Scopus, TRDizin)

90. Growth and relationship of phenotypic characteristics with gonadal pathology and tumour risk in patients with 45, X/46, XY mosaicism

Poyrazoglu Ş., Bas F., Karaman B., Yildiz M., Başaran S., Darendeliler F. F.

CLINICAL ENDOCRINOLOGY , vol.94, no.6, pp.973-979, 2021 (SCI-Expanded, Scopus)

91. LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency

Kardelen A. D., Kara M., Güller D., Ozturan E., Abalı Z., Ceylaner S., et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , vol.20, no.2, pp.389-394, 2021 (SCI-Expanded, Scopus) Sustainable Development

92. Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience.

Abali Z. Y., De Franco E., Karakilic Ozturan E., Poyrazoglu Ş., Bundak R., Bas F., et al.

Hormone research in paediatrics , vol.93, pp.423-432, 2021 (SCI-Expanded, Scopus) Sustainable Development

93. HEART AND AORTA ANOMALIES IN TURNER SYNDROME AND RELATION WITH KARYOTYPE

Al Kardelen A. D., Gencay G., BAYRAMOĞLU Z., Aliyev B., Karakilic-Ozturan E., POYRAZOĞLU Ş., et al.

ACTA ENDOCRINOLOGICA-BUCHAREST , vol.17, no.1, pp.124-130, 2021 (SCI-Expanded, Scopus) Sustainable Development

94. Clinical Alteration of Sleep Related Dissociative Disorder into Psychogenic Nonepileptic Seizure in an Adolescent Girl with The History of Physical Abuse in Early Childhood

Yetim A., Alnak A., Aydın Y. Ş., Güdek K., Yıldız İ., Baş F., et al.

Front med case rep , vol.02, no.02, pp.1-4, 2021 (Peer-Reviewed Journal)

95. Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

Dağdeviren Çakır A., Baş F., Akın O., Şıklar Z., Özcabı B., Berberoğlu M., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.13, no.3, pp.308-319, 2021 (SCI-Expanded, Scopus, TRDizin)

96. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants

GÜRAN T., Tezel B., Cakir M., AKINCI A., ORBAK Z., Keskin M., et al.

Journal of clinical research in pediatric endocrinology , vol.12, no.3, pp.287-294, 2020 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

97. **A Rare Cause of Adrenal Insufficiency - Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature**

Kardelen Al A. D., Al A. D. K., Poyrazoglu S., Poyrazoǧlu Ş., Aslanger A., Aslanger A. D., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.6, pp.395-403, 2020 (SCI-Expanded, Scopus) Sustainable Development

98. Superb Microvascular Imaging in the Evaluation of Pediatric Graves Disease and Hashimoto Thyroiditis.

Bayramoglu Z., Kandemirli S. G., Sari Z. N. A., Kardelen A. D., Poyrazoglu S., Bas F., et al.

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine , vol.39, pp.901-909, 2020 (SCI-Expanded, Scopus)

99. BASELINE CHARACTERISTICS OF PATIENTS WITH GROWTH HORMONE DEFICIENCY

Uckun U., Bas F., Poyrazoglu Ş., Sukur N. M., Darendeliler F. F., Bundak R.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.83, no.4, pp.413-420, 2020 (ESCI, TRDizin)

100. Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

Siklar Z., DEMİRCİOĞLU S., BEREKET A., BAŞ F., GÜRAN T., Akberzade A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.12, no.2, pp.150-159, 2020 (SCI-Expanded, Scopus, TRDizin)

101. A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent

Poyrazoglu S., Hwa V., Bas F., Dauber A., Rosenfeld R., Darendeliler F. F.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.11, no.4, pp.432-438, 2019 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

102. Serum endocan levels as a marker of endothelial dysfunction in Turner syndrome and correlation with cardiac findings

Gencay A. G., Darendeliler F. F., Nisli K., Karaca S., Kardelen A. D., Poyrazoglu S., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.244, 2019 (SCI-Expanded, Scopus)

103. Clinical characteristics and response to growth hormone treatment in patients with Prader-Willi Syndrome

Evliyaoglu O., Cakir A. D., Bas F., Akin O., ŞIKLAR Z., Ozcabi B., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.423, 2019 (SCI-Expanded, Scopus)

104. Follow-up of individuals with gender identity disorders: A long and challenging process

Ozturan E. K., Ozturk A. P., Kardelen A. A. D., Poyrazoglu S., Bas F., AYAZ A. B., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.486-487, 2019 (SCI-Expanded, Scopus)

105. Two siblings with hypophosphatemic rickets: SLC34A3 gene mutations with different clinical phenotypes

Karakilic-Ozturan E., Ozturk A. P., Kardelen A. A. D., Poyrazoglu S., Bas F., Darendeliler F. F.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.380, 2019 (SCI-Expanded, Scopus)

106. Genotype-Phenotype Correlation and Clinical Findings in 145 Patients with Congenital Adrenal Hyperplasia: Single Centre Experience

Cilsaat G., Toksoy G., Bas F., Karaman B., Poyrazoglu Ş., Uyguner O., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.282, 2019 (SCI-Expanded, Scopus)

107. Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency

Abali Z. Y., Yildiz M., Bas F., Onal H., ABALI S., Cilsaat G., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.205-206, 2019 (SCI-Expanded, Scopus)

108. The investigation of genetic etiology in familial cases with congenital hypothyroidism

Al A. D. K., Isik F. B., Ozturan E. K., Sozuguzel M. D., Ozturk A. P., Poyrazoglu S., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.199, 2019 (SCI-Expanded, Scopus)

109. Genetic Evaluation of Idiopathic Short Stature

Karaman B., Bas F., Najafli A., Avci S., Al A. D. K., Toksoy G., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.323, 2019 (SCI-Expanded, Scopus)

110. The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation

Ozturk A. P., Altunoglu U., Ozturan E. K., Toksoy G., Poyrazoglu S., Bas F., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.452, 2019 (SCI-Expanded, Scopus)

111. Targeted Panel Gene Sequencing for Identification of Genetic Etiology of 46, XY Disorders of Sex Development

Poyrazoglu S., Toksoy G., Aghayev A., Karaman B., Avci S., Altunoglu U., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.193, 2019 (SCI-Expanded, Scopus)

112. Determination of insulin resistance and its relationship with hyperandrogenemia,anti-Müllerian hormone, inhibin A, inhibin B, and insulin-like peptide-3 levels in adolescent girls with polycystic ovary syndrome.

Yetim Ş., BAS F., YETIM Ç., UÇAR A., POYRAZOGLU S., BUNDAK R., et al.

Turkish journal of medical sciences , vol.49, no.4, pp.1117-1125, 2019 (SCI-Expanded, Scopus, TRDizin)

113. Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.

Jolly A., Jolly A., Bayram Y., Bayram Y., DEMİRCİOĞLU S., Turan S., et al.

The Journal of clinical endocrinology and metabolism , vol.104, no.8, pp.3049-3067, 2019 (SCI-Expanded, Scopus)

114. üçüncü basamak bir pediatrik endokrinoloji merkezinde izlenen ağır boy kısalığı vakalarının etiyolojik değerlendirilmesi

uçkun u., BAŞ F., POYRAZOĞLU Ş., ŞÜKÜR N. M., DARENDELİLER F. F., bundak r.

ÇOCUK DERGİSİ , vol.19, pp.63-76, 2019 (TRDizin)

115. Etiologic Evaluation of Severe Short Stature in Children at Tertiary Pediatric Endocrinology Centre

Uçkun U., BAŞ F., POYRAZOĞLU Ş., ŞÜKÜR N. M., DARENDELİLER F. F., BUNDAK R.

Çocuk Dergisi , 2019 (TRDizin)

116. Measurement of serum vitamin B12-related metabolites in newborns: implications for new cutoff values to detect B12 deficiency.

Yetim A., Aygun E., Yetim C., Ucar A., Karakas Z., Gokcay G. F., et al.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians , pp.1-9, 2019 (SCI-Expanded, Scopus)

117. MULTI-PARAMETRIC ULTRASOUND EVALUATION OF PEDIATRIC THYROID DYSHORMONOGENESIS

ADALETLI I., BAYRAMOGLU Z., CALISKAN E., YILMAZ R. S., Akyol S., BAS F., et al.

ULTRASOUND IN MEDICINE AND BIOLOGY , vol.45, no.7, pp.1644-1653, 2019 (SCI-Expanded, Scopus)

118. THE ROLE OF THYROID FINE-NEEDLE ASPIRATION CYTOLOGY IN THE TREATMENT AND FOLLOW-UP OF THYROID NODULES IN THE PEDIATRIC POPULATION

KARDELEN A. D., YıLMAZ C., POYRAZOGLU S., TUNCA F., BAYRAMOGLU Z., BAS F., et al.

ACTA ENDOCRINOLOGICA-BUCHAREST , no.3, pp.333-341, 2019 (SCI-Expanded, Scopus)

119. Comparison of the Clinical and Anthropometric Features of Treated and Untreated Girls with Borderline Early Puberty.

DEMIRKALE Z., ABALı Z., BAS F., POYRAZOGLU S., BUNDAK R., Darendeliler F. F.

Journal of pediatric and adolescent gynecology , vol.32, pp.264-270, 2019 (SCI-Expanded, Scopus)

120. A novel 3' untranslated region mutation in the SLC29A3 gene associated with pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus syndrome.

Riachi M., Bas F., Darendeliler F. F., Hussain K.

Pediatric diabetes , vol.20, no.4, pp.474-481, 2019 (SCI-Expanded, Scopus) Sustainable Development

121. Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

EREN E., Ergur A. T., İŞGÜVEN Ş. P., Bitkin E. C., BERBEROĞLU M., ŞIKLAR Z., et al.

Journal of clinical research in pediatric endocrinology , vol.11, no.2, pp.149-156, 2019 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

122. Frequency of Ambiguous Genitalia in 14,177 Newborns in Turkey.

AYDIN B., SAKA N., BAS F., BAS E., COBAN A., YILDIRIM S., et al.

Journal of the Endocrine Society , vol.3, pp.1185-1195, 2019 (Scopus)

123. Joubert syndrome with multiple pituitary hormone deficiency.

Akcan N., Bas F., Poyrazoglu Ş., Bundak R.

BMJ case reports , vol.12, 2019 (ESCI, Scopus)

124. Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

Abaci A., Catli G., Kirbiyik O., ŞAHİN N., Abali Z. Y., Unal E., et al.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.42, no.4, pp.453-470, 2019 (SCI-Expanded, Scopus)

125. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants

GÜRAN T., TEZEL B., GÜRBÜZ F., Selver E., HATIPOĞLU N., KARA C., et al.

Journal of clinical research in pediatric endocrinology , vol.11, pp.13-23, 2019 (SCI-Expanded, Scopus, TRDizin)

126. Vitamin D and Nutritional Status of Children Evaluated via Bioelectric Impedance Analysis

Khalilova F., Ozcetin M., Kilic A., Bas F., Yetim A., Keskindemirci G., et al.

HONG KONG JOURNAL OF PAEDIATRICS , vol.24, no.1, pp.9-15, 2019 (SCI-Expanded, Scopus) Sustainable Development

127. Management of hypoglycemia in newborn: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report.

ALİEFENDİOĞLU D., Coban A., HATİPOĞLU N., Ecevit A., ARISOY A. E., Yesiltepe G., et al.

Turk pediatri arsivi , vol.53, 2018 (Scopus, TRDizin) Sustainable Development

128. Neonatal Hyperglycemia, which threshold value, diagnostic approach and treatment?: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report.

Simsek D. G., Ecevit A., HATİPOĞLU N., Coban A., ARISOY A. E., Bas F., et al.

Turk pediatri arsivi , vol.53, 2018 (Scopus, TRDizin) Sustainable Development

129. Endokrin Hastalıklarda Çocukluktan Erişkine Geçiş Deneyimi

Karakılıç Özturan E., Kardelen A. D., Öztürk A. P., Kubat Üzüm A., Özçetin M., Baş F., et al.

Çocuk Dergisi , vol.18, no.3, pp.129-134, 2018 (TRDizin)

130. Assessment of paediatric Hashimoto's thyroiditis using superb microvascular imaging

BAYRAMOGLU Z., KANDEMIRLI S. G., CALISKAN E., YILMAZ R. S., KARDELEN A. D., POYRAZOGLU S., et al.

CLINICAL RADIOLOGY , vol.73, no.12, 2018 (SCI-Expanded, Scopus)

131. Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 gene mutation: case report and review of possible mechanisms.

Bas F., Abali Z. Y., Toksoy G., Poyrazoglu S., Bundak R., Gulec Ç., et al.

Hormones (Athens, Greece) , vol.17, no.4, pp.581-588, 2018 (SCI-Expanded, Scopus)

132. Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

Poyrazoglu S., Bundak R., Abali Z. Y., ONAL H., SARIKAYA S., AKGUN A., et al.

Journal of clinical research in pediatric endocrinology , vol.10, no.4, pp.336-342, 2018 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

133. Body mass index at the presentation of premature adrenarche is associated with components of metabolic syndrome at puberty.

Kaya G., Abali Z. Y., Bas F., Poyrazoglu S., Darendeliler F. F.

European journal of pediatrics , vol.177, no.11, pp.1593-1601, 2018 (SCI-Expanded, Scopus) Sustainable Development

134. A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations

Kardelen A. D., Toksoy G., Bas F., Abali Z. Y., Gencay G., Poyrazoglu S., et al.

Journal of clinical research in pediatric endocrinology , vol.10, no.3, pp.206-215, 2018 (SCI-Expanded, Scopus, TRDizin)

135. Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene.

Baş F., Toksoy G., Ergun-Longmire B., Uyguner Z. O., Abalı Z., Poyrazoğlu Ş., et al.

The Journal of steroid biochemistry and molecular biology , vol.181, pp.88-97, 2018 (SCI-Expanded, Scopus)

136. Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings

AKCAN N., POYRAZOGLU S., BAS F., BUNDAK R., Darendeliler F. F.

Journal of clinical research in pediatric endocrinology , vol.10, pp.100-107, 2018 (SCI-Expanded, Scopus, TRDizin)

137. Glycemic control and health behaviors in adolescents with type 1 diabetes

Yetimi A., Alikasifoglu M., Bas F., Eliacik K., Cig G., Erginoz E., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.60, no.3, pp.244-254, 2018 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

138. Determinants of Increased Aortic Diameters in Young Normotensive Patients With Turner Syndrome Without Structural Heart Disease.

Ucar A., Tugrul M. Z., Erol B. O., Yekeler E., Aydin B., Yildiz S., et al.

Pediatric cardiology , vol.39, no.4, pp.786-793, 2018 (SCI-Expanded, Scopus)

139. Approach to hypoglycemia in the newborn: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report.(Yenidoğanda hipoglisemiye yaklaşım:Türk Neonatoloji ve Çocuk Endokrinolojive Diyabet Dernekleri uzlaşı raporu)

ALİEFENDİOĞLU D., ÇOBAN E. A., HATİPOĞLU N., ECEVİT A. N., ARISOY A. E., YEŞİLTEPE MUTLU R. G., et al.

Turkish Archives of Pediatrics , 2018 (Peer-Reviewed Journal)

140. Yenidoğan hiperglisemisi, hangi eşik değer, tanısal yaklaşım ve tedavi?:Tütk Neonatoloji ve Çocuk Endokrinoloji ve Diabet Dernekleri uzlaşı raporu (Neonatal Hyperglycemia, which threshold value, diagnostic approach and treatment?:Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies. consensus report)

GÖKŞEN ŞİMŞEK R. D., ECEVİT A. N., HATİPOĞLU N., ÇOBAN E. A., ARISOY A. E., BAŞ F., et al.

TURK PEDIATRI ARSIVI , vol.53, no.1, pp.234-238, 2018 (Scopus, TRDizin)

141. Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty.

CETINKAYA S., Poyrazoglu S., Bas F., Ercan O., Yıldız M., Adal E., et al.

Journal of pediatric endocrinology & metabolism : JPEM , vol.31, no.2, pp.175-184, 2018 (SCI-Expanded, Scopus)

142. Copy-Number Variations of the Human Olfactory Receptor Gene Family in Patients with Macromastia and Prepubertal Gynecomastia

Bas F., Karaman B., Kardelen A. A. D., Heidargholizadeh S., Najafli A., Toksoy G., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.560, 2018 (SCI-Expanded, Scopus)

143. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants

Guran T., Tezel B., Gurbuz F., Eklioglu B. S., HATİPOĞLU N., Kara C., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.141-142, 2018 (SCI-Expanded, Scopus)

144. Evaluation of Three Patients with 46,XY Gonadal Dysgenesis due to Desert Hedgehog Gene Mutations

Poyrazoglu S., Aghayev A., Toksoy G., Karaman B., Avci S., Kardelen A. A. D., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.558-559, 2018 (SCI-Expanded, Scopus)

145. Clinical, Laboratory and Molecular Genetic Findings of Patients with 17 beta-Hydroxysteroid Dehydrogenase 3 Deficiency

Poyrazoglu S., Toksoy G., Aghayev A., Karaman B., Avci S., Altunoglu U., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.562, 2018 (SCI-Expanded, Scopus)

146. Osteoporosis-Pseudoglioma Syndrome (OPPG): Improvement of Osteoporosis on Biphosphonate Therapy

Ozturan E. K., Altunoglu U., Kardelen A. D., Abali Z. Y., Avci S., Karabey H. K., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.181-182, 2018 (SCI-Expanded, Scopus)

147. Evaluation of Genetic Etiology in Patients with 46,XY Disorders of Sex Development: One Center Experience

Aghayev A., Toksoy G., Poyrazoglu S., Karaman B., Avci S., Yildiz M., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.542, 2018 (SCI-Expanded, Scopus)

148. Liver tissue trace element levels in HepB patients and the relationship of these elements with histological injury in the liver and with clinical parameters

SAHIN M., Karayakar F., ERDOĞAN K. E., Bas F., Colak T.

JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY , vol.45, pp.70-77, 2018 (SCI-Expanded, Scopus) Sustainable Development

149. PROKR2 Mutations in Patients With Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency

Najafli A., Bas F., Karaman B., Kardelen Al A. D., Toksoy G., Poyrazoglu S., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.500, 2018 (SCI-Expanded, Scopus)

150. Nationwide Hypophosphatemic Rickets Study

ŞIKLAR Z., DEMİRCİOĞLU S., BEREKET A., ABACI A., Bas F., DEMİR K., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.109-110, 2018 (SCI-Expanded, Scopus)

151. The Experience of Transition from Childhood to Adulthood in Endocrinology

KARAKILIÇ ÖZTURAN E., KARDELEN A. D., ÖZTÜRK A. P., KUBAT ÜZÜM A., ÖZÇETİN M., BAŞ F., et al.

Çocuk Dergisi , vol.18, pp.129-134, 2018 (TRDizin)

152. Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype

Kardelen A. D., Darendeliler F. F., Gencay G., Ince Z., Aliyev B., Ozturan E. K., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.433-434, 2018 (SCI-Expanded, Scopus)

153. Electrocardiographic changes in children with diabetic ketoacidosis and ketosis

Aygun D., Aygun F., Nisli K., Bas F., Citak A.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.52, no.4, pp.194-201, 2017 (ESCI, Scopus, TRDizin) Sustainable Development

154. Two novel mutations in XYLT2 cause spondyloocular syndrome.

Taylan F., Abali Z. Y., Jaentti N., Gunes N., Darendeliler F. F., Bas F., et al.

American journal of medical genetics. Part A , vol.173, no.12, pp.3195-3200, 2017 (SCI-Expanded, Scopus)

155. The relationship between infancy growth rate and the onset of puberty in both genders

Aydin B. K., Devecioglu E., Kadıoğlu A., CAKMAK A. E., Kisabacak S., Gokcay G., et al.

PEDIATRIC RESEARCH , vol.82, no.6, pp.940-946, 2017 (SCI-Expanded, Scopus)

156. Sonography and Magnetic Resonance Imaging Characteristics of Testicular Adrenal Rest Tumors

Yilmaz R. S., Sahin D., Aghayev A., Erole O. B., Poyrazoglu S., Saka N., et al.

POLISH JOURNAL OF RADIOLOGY , vol.82, pp.583-588, 2017 (ESCI, Scopus)

157. Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAF^V600E Mutation.

Poyrazoglu S., Bundak R., Bas F., Yegen G., Sanli Y., Darendeliler F. F.

Journal of clinical research in pediatric endocrinology , vol.9, no.3, pp.185-193, 2017 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

158. Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients.

Aydin B. K., Saka N., Bas F., Yilmaz Y., Haliloglu B., GÜRAN T., et al.

Journal of pediatric and adolescent gynecology , vol.30, no.4, pp.449-455, 2017 (SCI-Expanded, Scopus)

159. Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height

SAVAS-ERDEVE S., CETINKAYA S., Abali Z. Y., Poyrazoglu S., Bas F., Berberoglu M., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.7, pp.759-766, 2017 (SCI-Expanded, Scopus)

160. Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families.

Dinçsoy B., DINÇKAN N., GÜVEN Y., BAŞ F., ALTUNOĞLU U., KUVVETLI S., et al.

European journal of medical genetics , vol.60, pp.163-168, 2017 (SCI-Expanded, Scopus)

161. PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY

Abaci A., Catli G., KIRBIYIK O., SAHIN N. M., Abali Z. Y., Unal E., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.551-552, 2017 (SCI-Expanded, Scopus)

162. THE RELATIONSHIP OF OBESITY AND INSULIN RESISTANCE WITH HYPERANDROGENEMIA, ANTI-MULLERIAN HORMONE, INHIBIN A, INHIBIN B AND INSULIN-LIKE PEPTIDE-3 LEVELS IN PATIENTS WITH POLYCYSTIC OVARY SYNDROME

Yetim A., Bas F., Bundak R., Poyrazoglu S., Darendeliler F. F.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.170-171, 2017 (SCI-Expanded, Scopus) Sustainable Development

163. Prevelance of vitamin D and B12 deficiency in adolescence

YETİM A., TIKIZ C., BAŞ F.

Çocuk Dergisi , vol.17, pp.24-29, 2017 (Peer-Reviewed Journal)

164. UNCOVERING A NEW MECHANISM IN THE PIGMENTARY HYPERTRICHOSIS AND NON-AUTOIMMUNE DIABETES MELLITUS (PHID) SYNDROME INVOLVING THE 3 ' UTR

Riachi M., Darendeliler F., Bas F., Hussain K.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.55, 2017 (SCI-Expanded, Scopus) Sustainable Development

165. A RARE CAUSE OF CONGENITAL ADRENAL HYPERPLASIA: CLINICAL AND GENETIC FINDINGS AND FOLLOW-UP OF SIX PATIENTS WITH 17 HYDROXYLASE DEFICIENCY

Kardelen A. D., Bas F., Toksoy G., Poyrazoglu Ş., Bundak R., Altunoglu U., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.429-430, 2017 (SCI-Expanded, Scopus)

166. THE ASSESSMENT OF GROWTH HORMONE TREATMENT AND ADULT HEIGHT IN PATIENTS WITH GROWTH HORMONE DEFICIENCY

Poyrazoglu S., Vazgecer E. O., Bas F., Bundak R., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.495, 2017 (SCI-Expanded, Scopus)

167. INCREASED AORTIC DIAMETERS IN NORMOTENSIVE CHILDREN AND ADOLESCENTS WITH TURNER SYNDROME WITH EMPHASIS ON ASSOCIATIONS WITH B-TYPE NATRIURETIC PEPTIDE AND INSULIN-LIKE GROWTH FACTOR1

Ucar A., Aksakal M. Z., Erol B. O., Yekeler E., Bas F., Poyrazoglu S., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.210, 2017 (SCI-Expanded, Scopus)

168. Graves Hastalığından Sonra Gelişen Hashimoto Tiroiditi

GENENÇ M., POYRAZOĞLU Ş., YAVAŞ ABALI Z., BAŞ F., BUNDAK R., DARENDELİLER F. F.

Türkiye Klinikleri Journal of Case Report , vol.24, no.2, pp.45-47, 2016 (Peer-Reviewed Journal)

169. Anti-müllerian hormone and inhibin-a, but not inhibin-b or insulin-like peptide-3, may be used as surrogates in the diagnosis of polycystic ovary syndrome in adolescents: Preliminary results

YETIM A., YETIM Ç., Baş F., EROL O., ÇıĞ G., UCAR A., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.8, no.3, pp.288-297, 2016 (SCI-Expanded, Scopus, TRDizin)

170. The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study.

Siklar Z., Genens M., Poyrazoglu S., Bas F., Darendeliler F. F., Bundak R., et al.

Journal of clinical research in pediatric endocrinology , vol.8, no.3, pp.305-12, 2016 (SCI-Expanded, Scopus, TRDizin)

171. Diagnosis and management of pediatric adrenal insufficiency

Ucar A., Bas F., Saka N.

WORLD JOURNAL OF PEDIATRICS , vol.12, no.3, pp.261-274, 2016 (SCI-Expanded, Scopus)

172. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome.

SARI E., BEREKET A., YESILKAYA E., Bas F., Bundak R., Aydin B. K., et al.

American journal of medical genetics. Part A , no.4, pp.942-8, 2016 (SCI-Expanded, Scopus)

173. Graves Hastalığından Sonra Gelişen Hashiomoto Tiroiditi

GENENŞ M., POYRAZOĞLU Ş., YAVAŞ ABALI Z., BAŞ F., BUNDAK R., DARENDELİLER F. F.

TÜRKİYE KLİNİKLERİ JOURNAL OF CASE REPORT , 2016 (Peer-Reviewed Journal)

174. Çocukluk Çağı Tiroid Bezi Kanserleri Tanı ve Tedavi

POYRAZOĞLU Ş., BAŞ F.

Türkiye Klinikleri J Pediatr Sci , vol.12, no.2, pp.70-76, 2016 (Peer-Reviewed Journal)

175. Ergenlik ve Sosyal Çalışma

Güdek K., Yetim Şahin A., Baş F., Kılıç A.

Çocuk Dergisi , vol.16, pp.92-97, 2016 (Peer-Reviewed Journal)

176. Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort.

GURAN T., BUONOCORE F., SAKA N., OZBEK M., AYCAN Z., BEREKET A., et al.

The Journal of clinical endocrinology and metabolism , vol.101, pp.284-92, 2016 (SCI-Expanded, Scopus)

177. Effect of Gonadotropin Releasing Hormone Analogues (GnRHa) on Final Height in Girls with Borderline Early Puberty or Normal Physiological Puberty Depend on Bone Age Advancement and Predicted Height

Hizli Z., Bas F., Poyrazoglu S., Genens M., Abali Z. Y., Bundak R., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.436, 2016 (SCI-Expanded, Scopus)

178. Onset of Puberty in Healthy Boys is Associated with a Decreased BMI Compared to Values Prior to the Onset of Puberty

Bundak R., Darendeliler F. F., Bas F., Poyrazoglu S., Gunoz H., Neyzi O.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.290, 2016 (SCI-Expanded, Scopus)

179. Precocious Puberty in Patients with Primary Adrenal Insufficiency due to Melanocortin Receptor 2 Mutation

Bas F., Abali Z. Y., GÜRAN T., Genens M., Poyrazoglu S., Bundak R., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.418, 2016 (SCI-Expanded, Scopus)

180. The 3M Syndrome: A Cause of Pre- and Post-Natal Severe Growth Retardation

Genens M., Altunoglu U., Bas F., Poyrazoglu S., Abali Z. Y., Bundak R., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.465-466, 2016 (SCI-Expanded, Scopus)

181. Clinicopathological Characteristics of Papillary Thyroid Cancer in Children With Emphasis on the Pubertal Status and Association With BRAFV600E Mutation

Poyrazoglu S., Bundak R., Bas F., Darendeliler F. F.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.481, 2016 (SCI-Expanded, Scopus) Sustainable Development

182. Clinical Characteristics and Molecular Analysis of Patients with Neonatal Diabetes

Abali Z. Y., Bundak R., Bas F., De Franco E., Genens M., Poyrazoglu S., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.211, 2016 (SCI-Expanded, Scopus) Sustainable Development

183. Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children.

NEYZI O., BUNDAK R., GÖKÇAY G. F., GÜNÖZ H., FURMAN A., DARENDELILER F. F., et al.

Journal of clinical research in pediatric endocrinology , vol.7, pp.280-93, 2015 (SCI-Expanded, Scopus, TRDizin)

184. A Homozygous TPO Gene Duplication (c.1184_1187dup4) Causes Congenital Hypothyroidism in Three Siblings Born to a Consanguineous Family.

CANGUL H., AYDIN B., Bas F.

Journal of pediatric genetics , vol.4, pp.194-8, 2015 (ESCI)

185. Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group.

Darendeliler F. F., YESILKAYA E., BEREKET A., Bas F., Bundak R., SARI E., et al.

Journal of clinical research in pediatric endocrinology , vol.7, no.3, pp.183-91, 2015 (SCI-Expanded, Scopus, TRDizin)

186. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.

Bas F., Uyguner Z. O., Darendeliler F., Aycan Z., Çetinkaya E., Berberoglu M., et al.

Endocrine , vol.49, no.2, pp.479-91, 2015 (SCI-Expanded, Scopus)

187. An easily missed diagnosis: 17-alpha-hydroxylase/17,20-lyase deficiency

KÜÇÜKEMRE-AYDıN B., ÖĞRENDIL-YANAR Ö., BILGE I., Baş F., POYRAZOĞLU Ş., YıLMAZ A., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.57, no.3, pp.277-281, 2015 (SCI-Expanded, Scopus, TRDizin)

188. Increased arterial stiffness in young normotensive patients with Turner syndrome: associations with vascular biomarkers

Ucar A., Oz F., Bas F., Oflaz H., Nisli K., Tugrul M. Z., et al.

CLINICAL ENDOCRINOLOGY , vol.82, no.5, pp.719-727, 2015 (SCI-Expanded, Scopus)

189. A Thiamine Responsive Megaloblastic Anemia Presented with Hypertriglyceridemia and Autoimmune Diabetes

Yılmaz Y., Karakaş Z., Aydın B., Baş F., Ünüvar A., Karakaş Z., et al.

Exp Clin Endocrinol Diabetes Rep , no.2, pp.8-10, 2015 (Peer-Reviewed Journal)

190. Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

YESILKAYA E., BEREKET A., Darendeliler F. F., Bas F., Poyrazoglu S., Aydin B. K., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.1, pp.27-36, 2015 (SCI-Expanded, Scopus, TRDizin)

191. Epidemiologic Features of Type 1 Diabetic Patients between 0 and 18 Years of Age in Istanbul City

Demir F., Gunoz H., Saka N., Darendeliler F. F., Bundak R., Bas F., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.1, pp.49-56, 2015 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

192. Long-term endocrine evaluation of childhood brain tumors

Abalı Z. Y., BAŞ F., POYRAZOĞLU Ş., Akcan N., Genenş M., Bundak R., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.7, pp.22, 2015 (SCI-Expanded, Scopus, TRDizin)

193. A bactericidal agent used in attempts suicide İsoniazid

ÖZÇEKER D., HAŞLAK F., YETİM ŞAHİN A., ÇITAK A., BAŞ F., TAMAY Z. Ü.

Çocuk Dergisi , 2015 (Peer-Reviewed Journal) Sustainable Development

194. Comparative analysis of glucoinsulinemic markers and proinflammatory cytokines in prepubertal children born large-versus appropriate-for gestational age.

Cetin C., Bas F., Ucar A., Poyrazoglu S., Saka N., Bundak R., et al.

Endocrine , vol.47, no.3, pp.816-24, 2014 (SCI-Expanded, Scopus) Sustainable Development

195. Associations of Size at Birth and Postnatal Catch-up Growth Status With Clinical and Biomedical Characteristics in Prepubertal Girls With Precocious Adrenarche: Preliminary Results

Ucar A., Yackobovitch-Gavan M., Erol O. B., Yekeler E., Saka N., Bas F., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.99, no.8, pp.2878-2886, 2014 (SCI-Expanded, Scopus)

196. Sitting height and sitting height/height ratio references for Turkish children

Bundak R., Bas F., Furman A., Gunoz H., Darendeliler F., Saka N., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.173, no.7, pp.861-869, 2014 (SCI-Expanded, Scopus)

197. Evaluation of endocrine function in children admitted to pediatric intensive care unit

Aydin B. K., Demirkol D., Bas F., Turkoglu U., Kumral A., Karabocuoglu M., et al.

PEDIATRICS INTERNATIONAL , vol.56, no.3, pp.349-353, 2014 (SCI-Expanded, Scopus)

198. Pelvic ultrasound findings in prepubertal girls with precocious adrenarche born appropriate for gestational age

Ucar A., Erol O. B., Yekeler E., Yildiz İ., Bozlak S., Saka N., et al.

CLINICAL ENDOCRINOLOGY , no.5, pp.699-705, 2014 (SCI-Expanded, Scopus) Sustainable Development

199. Metabolic syndrome in young people

Poyrazoglu S., Bas F., Darendeliler F.

CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY , vol.21, no.1, pp.56-63, 2014 (SCI-Expanded, Scopus) Sustainable Development

200. ADHERENCE TO GROWTH HORMONE THERAPY: RESULTS OF A MULTICENTER STUDY

Aydin B. K., Aycan Z., Siklar Z., Berberoglu M., Ocal G., Çetinkaya S., et al.

ENDOCRINE PRACTICE , vol.20, no.1, pp.46-51, 2014 (SCI-Expanded, Scopus)

201. Z-Score Reference Values for Height in Turkish Children Aged 6 to 18 Years

Gunoz H., Bundak R., Furman A., Darendeliler F. F., Saka N., Bas F., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.1, pp.28-33, 2014 (SCI-Expanded, Scopus)

202. Netherton Syndrome Associated with Growth Hormone Deficiency

Aydin B. K., Bas F., Tamay Z. Ü., Kilic G., Suleyman A., Bundak R., et al.

PEDIATRIC DERMATOLOGY , vol.31, no.1, pp.90-94, 2014 (SCI-Expanded, Scopus)

203. Are metabolic syndrome antecedents in prepubertal children associated with being born idiopathic large for gestational age?

Cetin C., Ucar A., Bas F., Poyrazoglu Ş., Bundak R., Saka N., et al.

PEDIATRIC DIABETES , vol.14, no.8, pp.585-592, 2013 (SCI-Expanded, Scopus)

204. Frequency and severity of ketoacidosis at onset of autoimmune type 1 diabetes over the past decade in children referred to a tertiary paediatric care centre: potential impact of a national programme highlighted

Ucar A., Saka N., Bas F., Sukur M., Poyrazoglu Ş., Darendeliler F., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.26, pp.1059-1065, 2013 (SCI-Expanded, Scopus) Sustainable Development

205. The role of leptin, soluble leptin receptor, adiponectin and visfatin in insulin sensitivity in preterm born children in prepubertal ages.

Yanni D., Darendeliler F. F., Bas F., Aydin B. K., Coban A., Ince Z.

Cytokine , vol.64, no.1, pp.448-53, 2013 (SCI-Expanded, Scopus)

206. Osteoma cutis

Aydin B. K., Yazganoglu K. D., Baykal C., Buyukbabani N., Ucar A., Bas F., et al.

PEDIATRICS INTERNATIONAL , vol.55, no.2, pp.257-258, 2013 (SCI-Expanded)

207. Reduced atherogenic indices in prepubertal girls with precocious adrenarche born appropriate for gestational age in relation to the conundrum of DHEAS

Ucar A., Saka N., Bas F., HATİPOĞLU N., Bundak R., Darendeliler F. F.

ENDOCRINE CONNECTIONS , vol.2, no.1, pp.2-11, 2013 (SCI-Expanded, Scopus)

208. Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

Flanagan S. E., Xie W., Caswell R., Damhuis A., Vianey-Saban C., Akcay T., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , vol.92, no.1, pp.131-136, 2013 (SCI-Expanded, Scopus) Sustainable Development

209. Growth Hormone/Insulin-Like Growth Factor-1 Axis as Related to Body Mass Index in Patients with Idiopathic Short Stature

Cengiz P., Bas F., Atalar F., Ucar A., Darendeliler F., Akan G., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.5, no.1, pp.13-19, 2013 (SCI-Expanded, Scopus)

210. Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

Simsek D. G., Aycan Z., ÖZEN S., Cetinkaya S., Kara C., Abali S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.5, no.1, pp.20-26, 2013 (SCI-Expanded, Scopus) Sustainable Development

211. Sequential Use of Hydrocortisone and Dexamethasone in Prenatal Treatment of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Ucar A., Saka N., Bas F., Poyrazoglu Ş., Bundak R., Darendeliler F.

HORMONE RESEARCH IN PAEDIATRICS , vol.79, no.5, pp.323-324, 2013 (SCI-Expanded, Scopus)

212. Precocious adrenarche in children born appropriate for gestational age: is there a difference between genders?

Ucar A., Saka N., Bas F., Bundak R., Gunoz H., Darendeliler F.

EUROPEAN JOURNAL OF PEDIATRICS , vol.171, no.11, pp.1661-1666, 2012 (SCI-Expanded, Scopus)

213. No Effect of the IGF-1 Gene rs35767 and rs17032362 Polymorphisms in the Etiology of Idiopathic Short Stature

Tekcan D., Bas F., Atalar F., Aydin B. K., Akan G., Tarhan T., et al.

EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES , vol.120, no.7, pp.395-400, 2012 (SCI-Expanded, Scopus)

214. Thyroid Hormones in Children on Antiepileptic Therapy

Aygun F., Ekici B., Aydinli N., Aydin B. K., Bas F., Tatli B.

INTERNATIONAL JOURNAL OF NEUROSCIENCE , vol.122, no.2, pp.69-73, 2012 (SCI-Expanded, Scopus)

215. Is Premature Thelarche in the First Two Years of Life Transient?

Ucar A., Saka N., Bas F., Bundak R., Gunoz H., Darendeliler F.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.3, pp.140-145, 2012 (SCI-Expanded, Scopus)

216. Clinical and Laboratory Characteristics of Children Referred for Early Puberty: Preponderance in 7-8 Years of Age

Kılıç A., Durmus M. S., Unuvar E., Yildiz I., Aydin B. K., Ucar A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.4, pp.208-212, 2012 (SCI-Expanded, Scopus) Sustainable Development

217. Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

GÜRBÜZ F., KOTAN L. D., Mengen E., ŞIKLAR Z., BERBEROĞLU M., Dokmetas S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.3, pp.121-126, 2012 (SCI-Expanded, Scopus)

218. The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

Bas F., Darendeliler F., AYCAN Z., ÇETİNKAYA E., Berberoglu M., Siklar Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.77, no.2, pp.85-93, 2012 (SCI-Expanded, Scopus)

219. Permanent Neonatal Diabetes Mellitus: Same Mutation, Different Glycemic Control with Sulfonylurea Therapy on Long-Term Follow-up

Aydin B. K., Bundak R., Bas F., Maras H., Saka N., Gunoz H., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , no.2, pp.107-110, 2012 (SCI-Expanded, Scopus) Sustainable Development

220. The Distribution of Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism in the Turkish Population

Bas F., Kelesoglu F., Timirci O., Eryilmaz S. K., Bozkurt N., Aydin B. K., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.3, no.3, pp.126-131, 2011 (SCI-Expanded, Scopus)

221. Comparison of Lipid Profiles with AP0A1 MspI Polymorphism in Obese Children with Hyperlipidemia

Toptas B., Gormus U., Ergen A., Gurkan H., Kelesoglu F., Darendeliler F. F., et al.

IN VIVO , vol.25, no.3, pp.425-430, 2011 (SCI-Expanded, Scopus) Sustainable Development

222. İdyopatik boy kısalığı

DARENDELİLER F. F., Küçükemre Aydın B., BAŞ F.

ÇOCUK DERGİSİ , vol.11, no.4, pp.147-150, 2011 (Peer-Reviewed Journal)

223. 46,XY cinsel farklılaşma sorunlarına yaklaşım: Testosteron sentez kusurları

BAŞ F.

Türkiye Klinikleri Pediatrik Bilimler , vol.7, no.3, pp.35-43, 2011 (Peer-Reviewed Journal)

224. Ambulatory blood pressure monitoring and renal functions in term small-for-gestational age children

Bilge I., Poyrazoglu S., Bas F., Emre S., Sirin A., Gökalp S., et al.

PEDIATRIC NEPHROLOGY , vol.26, no.1, pp.119-126, 2011 (SCI-Expanded, Scopus)

225. Post-transplant glucose status in 61 pediatric renal transplant recipients: Preliminary results of five Turkish pediatric nephrology centers

Buyan N., Bilge I., Turkmen M. A., Bayrakci U., Emre S., Fidan K., et al.

PEDIATRIC TRANSPLANTATION , vol.14, no.2, pp.203-211, 2010 (SCI-Expanded, Scopus) Sustainable Development

226. Kriptorşidisi olan çocuğa yaklaşım

Küçükemre Aydın B., BAŞ F., DARENDELİLER F. F.

Klinik Tıp Pediatri , vol.2, no.1, pp.19-21, 2010 (Peer-Reviewed Journal)

227. Endocrine late effects of childhood cancer therapy

POYRAZOĞLU Ş., BAŞ F., Darendeliler E., DARENDELİLER F. F.

TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY , vol.25, no.1, pp.37-46, 2010 (ESCI, Scopus) Sustainable Development

228. Comparison of Lipid Profiles in Relation to APOB EcoRI Polymorphism in Obese Children with Hyperlipidemia

Timirci O., Darendeliler F., Bas F., Arzu E. H., Umit Z., Isbir T.

IN VIVO , vol.24, no.1, pp.65-69, 2010 (SCI-Expanded, Scopus) Sustainable Development

229. The international index of erectile function: Does mode of administration affect its psychometric properties?

Serefoglu E. C., Dogan B., Cimen H. L., BAŞ F.

JOURNAL OF SEXUAL MEDICINE , vol.6, pp.444, 2009 (SCI-Expanded, Scopus)

230. Investigation of impaired carbohydrate metabolism in pediatric liver transplant recipients

Gokce S., Durmaz Ö., Celtik C., Aydogan A., Bas F., Turkoglu U., et al.

PEDIATRIC TRANSPLANTATION , vol.13, no.7, pp.873-880, 2009 (SCI-Expanded, Scopus) Sustainable Development

231. The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children

GÜRAN T., Turan S., BEREKET A., Akcay T., Unluguzel G., Bas F., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.168, no.9, pp.1043-1048, 2009 (SCI-Expanded, Scopus) Sustainable Development

232. Diagnostic spectrum of congenital hypothyroidism in Turkish children

Tamam M., Adalet I., Bakir B., Tuerkmen C., Darendeliler F., Bas F., et al.

PEDIATRICS INTERNATIONAL , vol.51, no.4, pp.464-468, 2009 (SCI-Expanded, Scopus)

233. No Activating Mutations of FSH Receptor in Four Children with Ovarian Juvenile Granulosa Cell Tumors and the Association of These Tumors with Central Precocious Puberty

Bas F., Pescovitz O. H., Steinmetz R.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , vol.22, no.3, pp.173-179, 2009 (SCI-Expanded, Scopus)

234. Ghrelin levels are decreased in non-obese prepubertal children born large for gestational age

Darendeliler F. F., Poyrazoglu Ş., Bas F., Sancakli O., Gokcay G.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.160, no.6, pp.951-956, 2009 (SCI-Expanded, Scopus)

235. Adiponectin is an indicator of insulin resistance in non-obese prepubertal children born large for gestational age (LGA) and is affected by birth weight

Darendeliler F. F., Poyrazoglu Ş., Sancakli O., Bas F., Gokcay G., Aki S., et al.

CLINICAL ENDOCRINOLOGY , vol.70, no.5, pp.710-716, 2009 (SCI-Expanded, Scopus)

236. A patient with 22q11.2 deletion syndrome: case report

Kabataş Eryılmaz S., BAŞ F., Satan A., DARENDELİLER F. F., BUNDAK R., Günöz H., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.1, no.3, pp.151-154, 2009 (Scopus)

237. Type 1 diabetes mellitus associated with autoimmune thyroid disease, celiac disease and familial Mediterranean fever: case report

Bas F., Kabatas-Eryilmaz S., Gunoz H., Darendeliler F., Kucukemre B., Bundak R., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.51, no.2, pp.183-186, 2009 (SCI-Expanded, Scopus) Sustainable Development

238. GENETIC ASPECTS OF HYPERINSULINISM IN INFANCY AND RESPONSE TO THERAPY

Darendeliler F. F., Bas F.

IUBMB LIFE , vol.61, no.3, pp.300, 2009 (SCI-Expanded, Scopus)

239. CYP21A2 GENE MUTATIONS IN CONGENITAL ADRENAL HYPERPLASIA: GENOTYPE-PHENOTYPE CORRELATION

Saka N.

IUBMB LIFE , vol.61, no.3, pp.301, 2009 (SCI-Expanded, Scopus)

240. COMPARISON OF LIPID PROFILES WITH APO A-I MSPI POLYMORPHISM ON OBESE CHILDREN WITH HYPERLIPIDEMIA BY USING DGGE

Toptas B., Darendeliler F. F., Bas F., Isbir T.

IUBMB LIFE , vol.61, no.3, pp.319-320, 2009 (SCI-Expanded, Scopus)

241. CYP21A2 gene mutations in congenital adrenal hyperplasia: Genotype-phenotype correlation in Turkish children

BAŞ F., Kayserili H., DARENDELİLER F. F., BUNDAK R., UYGUNER Z. O., GÜNÖZ H., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.1, no.3, pp.116-128, 2009 (Scopus)

242. COMPARISON OF LIPID PROFILE WITH APO B-100 ECORI POLYMORPHISM ON OBESE CHILDREN WITH HYPERLIPIDEMIA BY USING DENATURATING GRADIENT GEL ELECTROPHORESIS

Timirci O., Darendeliler F. F., Bas F., Isbir T.

IUBMB LIFE , vol.61, no.3, pp.322, 2009 (SCI-Expanded, Scopus)

243. Boy kısalığı olan çocuğa yaklaşım

Küçükemre Aydın B., BAŞ F., DARENDELİLER F. F.

Klinik Tıp Pediatri , vol.1, no.1, pp.30-36, 2009 (Peer-Reviewed Journal)

244. Target Height Estimation in Children with Idiopathic Short Stature Who Are Referred to the Growth Clinic

Poyrazoglu S., Darendeliler F., Bas F., Bundak R., Saka N., DARCAN Ş., et al.

HORMONE RESEARCH , vol.72, no.3, pp.178-183, 2009 (SCI-Expanded, Scopus)

245. Molecular analysis of PIT1, PROP1, LHX3, and HESX1 in patients with combined pituitary hormone deficiency: multicenter study

Bas F., Darendeliler F. F., Oyguner O., Aycan Z., Cetinkaya E., BERBEROĞLU M., et al.

HORMONE RESEARCH , vol.72, pp.396-397, 2009 (SCI-Expanded)

246. The relationship between IGF-1 response and 1st year height velocity on two different doses of GH in idiopathic GH deficiency (IGHD): a randomized, prospective clinical study

Bundak R., Arslanoglu I., Berberoglu M., Siklar Z., Isguven P., Ocal G., et al.

HORMONE RESEARCH , vol.72, pp.104-105, 2009 (SCI-Expanded)

247. CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish children.

Baş F., Kayserili H., Darendeliler F., Uyguner O., Günöz H., Yüksel A., et al.

Journal of clinical research in pediatric endocrinology , vol.1, pp.116-28, 2009 (SCI-Expanded, Scopus)

248. Serum IGF-1 and IGFBP-3 levels in healthy Turkish children between 0-6 years of age

YÜKSEL B., Ozbek M. N., Darendeliler F. F., BİDECİ A., Cetinkaya E., BERBEROĞLU M., et al.

HORMONE RESEARCH , vol.72, pp.261, 2009 (SCI-Expanded)

249. The exon 3 deleted/full length growth hormone receptor polymorphism and response to GH therapy in GH deficiency and Turner syndrome: a multicenter study

Darendeliler F. F., Bas F., Bozkurt N., Uzunhan O., Aycan Z., Cetinkaya E., et al.

HORMONE RESEARCH , vol.72, pp.109, 2009 (SCI-Expanded)

250. Evaluation of Adrenomedullary Function in Patients with Congenital Adrenal Hyperplasia

Tutunculer F., Saka N., Arkaya S. C., Abbasoglu S., Bas F.

HORMONE RESEARCH , vol.72, no.6, pp.331-336, 2009 (SCI-Expanded, Scopus)

251. The distribution of exon 3-deleted/full-length growth hormone receptor polymorphism in Turkish population

Bas F., Kelesoglu F., Eryilmaz S. K., Darendeliler F. F., Aydin B. K., Timirci O., et al.

HORMONE RESEARCH , vol.72, pp.87, 2009 (SCI-Expanded)

252. Resistance to thyroid hormone in a Turkish child with A317T mutation in the thyroid hormone receptor-beta gene

Poyrazoglu S., Tuetuencueler F., Bas F., Darendeliler F.

TURKISH JOURNAL OF PEDIATRICS , vol.50, no.6, pp.577-580, 2008 (SCI-Expanded, Scopus)

253. Elevated ghrelin levels in preterm born children during prepubertal ages and relationship with catch-up growth.

Darendeliler F., Bas F., Bundak R., Coban A., Disci R., Sancakli O., et al.

European journal of endocrinology , vol.159, no.5, pp.555-60, 2008 (SCI-Expanded, Scopus) Sustainable Development

254. Adult height in Turkish patients with Turner syndrome without growth hormone treatment

BEREKET A., Turan S., Elcioglu N., Hacihanefioglu S., Memioğlu N., Bas F., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.50, no.5, pp.415-417, 2008 (SCI-Expanded, Scopus)

255. Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients

Poyrazoglu S., Saka N., Bas F., İşgüven P., Dogu A., Turan S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.8, pp.745-751, 2008 (SCI-Expanded, Scopus) Sustainable Development

256. Insulin, adiponectin, IGFBP-1 levels and body composition in small for gestational age born non-obese children during prepubertal ages

Sancakli O., Darendeliler F., Bas F., Gokcay G., Disci R., Aki S., et al.

CLINICAL ENDOCRINOLOGY , vol.69, no.1, pp.88-92, 2008 (SCI-Expanded, Scopus)

257. The effect of growth hormone treatment on head circumference in growth hormone-deficient children

Darendeliler F., Bas F., Goekce M., Poyrazoglu Ş., Bundak M. S. R., Saka N., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.50, no.4, pp.331-335, 2008 (SCI-Expanded, Scopus)

258. Hipoglisemi

Küçükemre Aydın B., BAŞ F.

Klinik Tıp Pediatri , vol.2, no.6, pp.8-16, 2008 (Peer-Reviewed Journal)

259. Successful Results of Pamidronate Treatment in Children With Osteogenesis Imperfecta With Emphasis on the Interpretation of Bone Mineral Density for Local Standards

Poyrazoglu S., Gunoz H., Darendeliler F., Bas F., Tutunculer F., Eryilmaz S. K., et al.

JOURNAL OF PEDIATRIC ORTHOPAEDICS , vol.28, no.4, pp.483-487, 2008 (SCI-Expanded, Scopus)

260. Çocuk ve ergenlik döneminde hipertiroidi

BAŞ F.

ÇOCUK DERGİSİ , vol.8, pp.25-33, 2008 (TRDizin)

261. Türk çocuklarında vücut ağırlığı, boy uzunluğu, baş çevresi ve vücut kitle indeksi referans değerleri

Neyzi O., Günöz H., Furman A., BUNDAK R., Gökçay G., DARENDELİLER F. F., et al.

ÇOCUK SAĞLIĞI VE HASTALIKLARI DERGİSİ , vol.51, pp.1-14, 2008 (Scopus)

262. Çocuk ve ergenlerde hipertansiyon: etiyoloji ve tanı

BAŞ F.

ÇOCUK DERGİSİ , vol.8, pp.70-74, 2008 (TRDizin)

263. Çocuk ve ergenlerde kalsiyum metabolizması bozuklukları

BAŞ F.

ÇOCUK DERGİSİ , vol.8, pp.55-69, 2008 (TRDizin)

264. Vitamin D bağımlı rahitis tipI ve tip II

DARENDELİLER F. F., BAŞ F., HANÇERLİ S.

Türkiye Klinikleri J Pediatr Sci , vol.4, no.5, pp.51-55, 2008 (Peer-Reviewed Journal)

265. Insulin resistance and body composition in preterm born children during prepubertal ages.

Darendeliler F., Bas F., Bundak R., Coban A., Sancakli O., Eryilmaz S. K., et al.

Clinical endocrinology , vol.68, no.5, pp.773-9, 2008 (SCI-Expanded, Scopus)

266. The effect of growth hormone treatment on bone mineral density in prepubertal girls with Turner syndrome: a multicentre prospective clinical trial

Aycan Z., Çetinkaya E., Darendeliler F. F., Vidinlisan S., Bas F., Bideci A., et al.

CLINICAL ENDOCRINOLOGY , vol.68, no.5, pp.769-772, 2008 (SCI-Expanded, Scopus)

267. Catch-up growth in appropriate- or small-for-gestational age preterm infants.

Darendeliler F. F., Çoban A., Bas F., Bundak R., Disci R., Suekuer M., et al.

The Turkish journal of pediatrics , vol.50, no.3, pp.207-13, 2008 (SCI-Expanded, Scopus)

268. Çocukluk dönemi santral diyabetes insipidus vakalarının etiyolojik değerlendirmesi

ERSOY M., DARENDELİLER F. F., BAŞ F., BUNDAK R., Saka H. N., Günöz H.

ÇOCUK DERGİSİ , vol.8, no.4, pp.217-220, 2008 (TRDizin) Sustainable Development

269. Mandibuloakral displazi: Vaka sunumu ve laminopatilere genel bakış

Pehlivan D., BAŞ F., Rosti R. Ö., DARENDELİLER F. F., KAYSERİLİ H.

ÇOCUK DERGİSİ , vol.8, no.4, pp.251-256, 2008 (Peer-Reviewed Journal)

270. Çocukluk ve ergenlik döneminde adrenal yetersizlik

BAŞ F., Eryılmaz Kabataş S.

Güncel Çocuk Sağlığı , vol.1, no.3, pp.9-26, 2008 (Peer-Reviewed Journal)

271. Preterm doğan çocuklarda prepubertal dönemde insülin direncinin değerlendirilmesi

DARENDELİLER F. F., BAŞ F., BUNDAK R., ÇOBAN E. A., Baş N., Sancaklı Ö., et al.

ÇOCUK DERGİSİ , vol.8, no.2, pp.0-92, 2008 (TRDizin)

272. Bone mineral density in children with acute lymphoblastic leukemia during consolidation treatment

Dogan E., Saribeyoglu E., Bas F., Darendeliler F. F., Agaoglu L.

HORMONE RESEARCH , vol.70, pp.187, 2008 (SCI-Expanded)

273. Puberty and pubertal growth in healty Turkish girls: no evidence for secular trend

BUNDAK R., DARENDELİLER F. F., GÜNÖZ H., BAŞ F., SAKA H. N., NEYZİ O.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.1, pp.8-14, 2008 (Scopus)

274. Elevated Ghrelin levels in preterm born children during prepubertal ages and relationship with catch up growth

DARENDELILER F. F., Bas F., Coban A., Disci R., SANCAKLI O., Gokcay G., et al.

HORMONE RESEARCH , vol.70, pp.148, 2008 (SCI-Expanded)

275. Prevalance of testicular microlithiasis in patients with congenital adrenal hyperplasia

Saka N., Poyrazoglu S., Agayev A., Yekeler E.

HORMONE RESEARCH , vol.70, pp.214-215, 2008 (SCI-Expanded)

276. Which target height estimation is appropriate for children with idiopathic short stature?

Poyrazoglu S., Darendeliler F. F., Bas F., Bundak R., DARCAN Ş., Sukur M., et al.

HORMONE RESEARCH , vol.70, pp.116, 2008 (SCI-Expanded)

277. Adiponectin as an early indicator of insulin resistance in non-obese prepubertal children born large for gestational age

Darendeliler F. F., Poyrazoglu S., Bas F., Sancakli O., Gokcay G., Bas N., et al.

HORMONE RESEARCH , vol.70, pp.62, 2008 (SCI-Expanded)

278. CYP21 gene mutations in congenital adrenal hyperplasia: Genotype-phenotype correlation in Turkish children

Bas F., Darendeliler F. F., Kayserili H., Uyguner O., Wollnik B., Saka N., et al.

HORMONE RESEARCH , vol.70, pp.156-157, 2008 (SCI-Expanded)

279. Effect of hypo- and euthyroid status on serum cystatin C levels

Tekerek H., Ozden T. A., Bas F., Darendeliler F. F.

HORMONE RESEARCH , vol.70, pp.168-169, 2008 (SCI-Expanded)

280. Ambulatory blood pressure monitoring in children with small for gestational age: the preliminary results of one center study

Gokalp S., Bilge I., Kabatas S., Bas F., Emre S., Darendeliler F. F.

PEDIATRIC NEPHROLOGY , vol.22, no.9, pp.1499, 2007 (SCI-Expanded, Scopus)

281. Analysis of puberty and pubertal growth in healthy boys

Bundak R., Darendeliler F. F., Günöz H., Bas F., Saka N., Neyzi O.

EUROPEAN JOURNAL OF PEDIATRICS , vol.166, no.6, pp.595-600, 2007 (SCI-Expanded, Scopus)

282. Corticotropin and cortisol response to maximal exercise testing in central diabetes insipidus

Bas F., Darendeliler F. F., Tatli B., Unal M., Kayserilioglu A.

PEDIATRICS INTERNATIONAL , vol.49, no.1, pp.53-57, 2007 (SCI-Expanded, Scopus) Sustainable Development

283. Comparison of the effect two modes of hCG stimulation on testicular descent and on plasma testosterone levels in children true unilateral cryptorchidism

BUNDAK R., ERMİŞ B., BAŞ F., DARENDELİLER F. F.

INTERNATIONAL PEDIATRICS , vol.22, no.1, pp.8-12, 2007 (Peer-Reviewed Journal)

284. Effects of growth hormone on growth, insulin resistance and related hormones (ghrelin, leptin and adiponectin) in Turner syndrome

Darendeliler F. F., Aycan Z., Çetinkaya E., Vidilisan S., Bas F., Bideci A., et al.

HORMONE RESEARCH , vol.68, no.1, pp.1-7, 2007 (SCI-Expanded, Scopus)

285. Growth references for Turkish children aged 6 to 18 years

Neyzi O., Furman A., Bundak R., Gunoz H., Darendeliler F. F., Bas F.

ACTA PAEDIATRICA , vol.95, no.12, pp.1635-1641, 2006 (SCI-Expanded, Scopus)

286. Evaluation of glucose intolerance in adolescents relative to adults with type 2 diabetes mellitus

Babaoglu K., Hatun S., Arslanoglu I., İşgüven P., Bas F., Ercan O., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.19, no.11, pp.1319-1326, 2006 (SCI-Expanded, Scopus) Sustainable Development

287. Ergenlik Gecikmesi

BAŞ F., POYRAZOĞLU Ş., DARENDELİLER F. F.

Türkiye Klinikleri Pediatrik Bilimler , vol.2, no.10, pp.24-31, 2006 (Peer-Reviewed Journal)

288. Event related potentials in girls with congenital adrenal hyperplasia

Isoglu-Alkac U., Gunoz H., Karamursel S., Bas F.

INTERNATIONAL JOURNAL OF PSYCHOPHYSIOLOGY , vol.61, no.3, pp.334, 2006 (SCI-Expanded)

289. Hyperinsulinism in infancy Genetic aspects

DARENDELİLER F. F., BAŞ F.

Pediatr Endocrinol Rev , vol.3, pp.521-526, 2006 (Scopus)

290. Çocuk ve ergende hipertiroidizm

BAŞ F.

ÇOCUK DERGİSİ , vol.6, pp.132-138, 2006 (TRDizin)

291. Hiperinsulinism in infancy-Genetic aspects

BAŞ F., DARENDELİLER F. F.

PEDIATRIC ENDOCRINOLOGY REV , vol.3, pp.521-526, 2006 (Peer-Reviewed Journal)

292. Worster-Drought syndrome (congenital bilateral perisylvian syndrome) with posterior pituitary ectopia, pituitary hypoplasia, empty sella and panhypopituitarism: A patient report

Bas F., Darendeliler F. F., Yapıcı Z., Gökalp S., Bundak R., Sakai N., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.19, no.4, pp.535-540, 2006 (SCI-Expanded, Scopus) Sustainable Development

293. Body mass index references for Turkish children

Bundak R., Furman A., Gunoz H., Darendeliler F. F., Bas F., Neyzi O.

ACTA PAEDIATRICA , vol.95, no.2, pp.194-198, 2006 (SCI-Expanded, Scopus) Sustainable Development

294. Effects of growth hormone treatment on ghrelin, leptin and adiponectin levels in Turner syndrome

Demirel F., Aycan Z., Cetinkaya E., Vidinlisan S., Bas F., Bideci A., et al.

HORMONE RESEARCH , vol.65, pp.188, 2006 (SCI-Expanded)

295. Evaluation of insulin resistance and leptin, ghrelin, adiponectin levels in children with classic congenital adrenal hyperplasia

Bas F., Gunoz H., Darendeliler F. F., Bundak R., Eryilmaz S. K., Poyrazoglu S., et al.

HORMONE RESEARCH , vol.65, pp.119, 2006 (SCI-Expanded)

296. Evaluation of adrenomedullary function in patients with congenital adrenal hyperplasia (CAH)

Tutunculer F., Saka N., Can S. A., Abbasoglu S., Bas F., Gunoz H.

HORMONE RESEARCH , vol.65, pp.118, 2006 (SCI-Expanded)

297. The properties of brain cognitive processing in girls with congenital adrenal hyperplasia

Gunoz H., Alkac U. I., Bas F., Karamursel S.

HORMONE RESEARCH , vol.65, pp.118-119, 2006 (SCI-Expanded)

298. Body composition in prepubertal children with respect to their birth weights

Sancakli O., Darendeliler F. F., Bas F., Gokcay G., Aki S., Eskiyurt N.

HORMONE RESEARCH , vol.65, pp.142, 2006 (SCI-Expanded)

299. Factors associated with obesity in children with hypothalamo-pituitary tumors

DEMİRCİOĞLU S., BEREKET A., Guran T., Akcay T., Gunoz H., Saka N., et al.

HORMONE RESEARCH , vol.65, pp.83, 2006 (SCI-Expanded) Sustainable Development

300. Insulin resistance and IGF-IGFBP axis in prepubertal children with respect to their birth weights

Sancakli O., Darendeliler F. F., Bas F., Gokcay G.

HORMONE RESEARCH , vol.65, pp.55, 2006 (SCI-Expanded)

301. Evaluation of patients with Graves' disease

Poyrazoglu S., Saka N., Bas F., Isguven P., Dogu A., Turan S., et al.

HORMONE RESEARCH , vol.65, pp.41, 2006 (SCI-Expanded)

302. Evaluation of insulin resistance in preterm born children in prepuberty

Darendeliler F. F., Bundak R., Bas F., Coban A., Kucukemre B., Ince Z., et al.

HORMONE RESEARCH , vol.65, pp.67-68, 2006 (SCI-Expanded)

303. Evaluation of insulin-like growth factor (IGF)-I and IGF binding protein-3 generation test in short stature

Darendeliler F. F., OCAL C., BAS F.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.18, no.5, pp.443-452, 2005 (SCI-Expanded, Scopus)

304. Weismann-Netter-Stuhl syndrome in two siblings

Yekeler E., Özdemir C., Gökalp S., Yıldırım A., Bas F., Günöz H., et al.

SKELETAL RADIOLOGY , vol.34, no.3, pp.176-179, 2005 (SCI-Expanded, Scopus)

305. Constitutional delay of growth and puberty: From presentation to final height

Poyrazoglu F., GÜNÖZ H., Darendeliler F. F., Saka N., Bundak R., Bas F.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.18, no.2, pp.171-179, 2005 (SCI-Expanded, Scopus)

306. Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: An analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

Darendeliler F., Berberoglu M., Ocal G., Adiyaman P., Bundak R., Gunoz H., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.18, no.10, pp.949-954, 2005 (SCI-Expanded, Scopus)

307. Turner sendromunda büyüme hormonu tedavi sonuçlarının değerlendirilmesi: Türkiye KIGS (Pfizer Uluslararası Büyüme Veri Tabanı) veri tabanı analiz sonuçları

DARENDELİLER F. F., BAŞ F., Berberoğlu M., ÖCAL G., Günöz H., Darcan Ş., et al.

ÇOCUK DERGİSİ , vol.5, no.1, pp.21-26, 2005 (TRDizin)

308. Transient Pseudohypoaldosteronism in an infant with urinary tract anomaly

Tütüncüler F., Günöz H., Bas F., Bundak R., Saka N., Neyzi O.

PEDIATRICS INTERNATIONAL , vol.46, no.5, pp.618-620, 2004 (SCI-Expanded, Scopus)

309. Reevaluation of growth hormone deficiency during and after growth hormone (GH) treatment: Diagnostic value of GH tests and IGF-I and IGFBP-3 measurements

Darendeliler F., Spinu I., Bas F., Bundak R., Isguven P., Arslanoglu I., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.17, no.7, pp.1007-1012, 2004 (SCI-Expanded, Scopus)

310. Diyet dondurmanın diyabetik çocukların kan şekeri düzeyine etkisi

Günöz H., Garipağaoğlu M., BAŞ F., BUNDAK R., Yılmaz S.

ÇOCUK DERGİSİ , vol.4, no.3, pp.149-152, 2004 (TRDizin) Sustainable Development

311. Büyüme hormonu eksikliği etyolojisi, demografik veriler ve tedavi sonuçlarının değerlendirilmesi: Türkiye verileri. KIGS (Pfizer Uluslar arası büyüme veri tabanı) analiz sonuçları

DARENDELİLER F. F., Berberoğlu M., Öcal G., Adıyaman P., BUNDAK R., Saka H. N., et al.

ÇOCUK DERGİSİ , vol.4, no.3, pp.141-148, 2004 (TRDizin)

312. Tip I diyabetli çocuklarda büyüme ve püberte

POYRAZOĞLU Ş., Saka H. N., BUNDAK R., BAŞ F., DARENDELİLER F. F., Günöz H.

ÇOCUK DERGİSİ , vol.4, no.2, pp.83-87, 2004 (TRDizin) Sustainable Development

313. A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency

TÜKEL T., Uyguner O., Wei J., Yüksel-Apak M., Saka N., Song D., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.88, no.12, pp.5893-5897, 2003 (SCI-Expanded, Scopus)

314. ABCC8 (SUR1) and KCNJ11 (KIR6.2) mutations in persistent hyperinsulinemic hypoglycemia of infancy and evaluation of different therapeutic measures

Darendeliler F. F., Fournet J., Bas F., Junien C., Gross M., Bundak R., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.15, no.7, pp.993-1000, 2002 (SCI-Expanded, Scopus)

315. Follow-up height after discontinuation of growth hormone treatment in children with intrauterine growth retardation

Darendeliler F. F., Bundak R., Kabatas S., Günöz H., Bas F., Saka N.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.15, no.6, pp.795-800, 2002 (SCI-Expanded, Scopus) Sustainable Development

316. Familial secundum atrial septal defect with dysrhythmia associated with web neck

Kilic Z., Ucar B., Bas F., DİNLEYİCİ E. Ç., Sari E.

TURKISH JOURNAL OF PEDIATRICS , vol.44, no.1, pp.69-72, 2002 (SCI-Expanded, Scopus)

317. Growth hormone treatment in short children with intrauterine growth retardation

Bundak R., Darendeliler F. F., Gunoz H., Bas F., Saka N., Neyzi O.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.14, no.3, pp.313-318, 2001 (SCI-Expanded, Scopus)

318. The effect of growth hormone treatment on biochemical indices in hypophosphatemic rickets

Darendeliler F. F., Bas F., Karaaslan N., Hekim N., Bundak R., Saka N., et al.

HORMONE RESEARCH , vol.55, no.4, pp.191-195, 2001 (SCI-Expanded, Scopus) Sustainable Development

319. Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children.

Bilge I., Kayserili H., Emre S., Nayir A., Sirin A., Tukel T., et al.

Pediatric nephrology (Berlin, Germany) , vol.14, no.12, pp.1111-4, 2000 (SCI-Expanded, Scopus)

320. Glucocorticoid receptors in patients with congenital adrenal hyperplasia

Saka N., Guven M., Bas F., Darendeliler F. F., Bundak R., Gunoz H., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.13, no.8, pp.1101-1107, 2000 (SCI-Expanded, Scopus)

321. Kuşkulu genitalyalı 103 hastanın etyoloji, tanı ve cinsel kimlik açısından değerlendirilmesi

DARENDELİLER F. F., BAŞ F., Saka H. N., KAYSERİLİ H., Apak M., Karaaslan N., et al.

KLİNİK GELİŞİM , vol.13, pp.109-114, 2000 (Peer-Reviewed Journal)

322. Bilateral ovarian steroid cell tumor in congenital adrenal hyperplasia due to classic 11 beta-hydroxylase deficiency

Bas F., Saka N., Darendeliler F. F., Tuzlali S., Ilhan R., Bundak R., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.13, no.6, pp.663-667, 2000 (SCI-Expanded, Scopus)

323. HLA-DR and -DQ associations with insulin-dependent diabetes mellitus in a population of Turkey

SARUHAN-DIRESKENELI G., UYAR F. A., BAS F., GUNOZ H., BUNDAK R., SAKA N., et al.

HUMAN IMMUNOLOGY , vol.61, no.3, pp.296-302, 2000 (SCI-Expanded, Scopus) Sustainable Development

324. Tuberculin reactivity in young children following neonatal BCG vaccination

Gokcay G., Partalci A., Bas F., Neyzi O.

JOURNAL OF TROPICAL PEDIATRICS , vol.46, no.1, pp.51-52, 2000 (SCI-Expanded, Scopus) Sustainable Development

325. Successful therapy with calcium channel blocker (nifedipine) in persistent neonatal hyperinsulinemic hypoglycemia of infancy

Bas F., Darendeliler F. F., Demirkol D., BUNDAK R., Saka N., Günöz H.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.12, no.6, pp.873-878, 1999 (SCI-Expanded, Scopus)

326. Deflazacort treatment in progressive diaphyseal dysplasia (Camurati-Engelmann disease)

Bas F., Darendeliler F. F., Petorak İ., Sadıkoğlu B., BİLİR A., Bundak R., et al.

JOURNAL OF PAEDIATRICS AND CHILD HEALTH , vol.35, no.4, pp.401-405, 1999 (SCI-Expanded, Scopus)

327. Evaluation of gonadal function in 107 intersex patients by means of serum antimullerian hormone measurement

Rey R., Belville C., Nihoul-Fekete C., Michel-Calemard L., Forest M., Lahlou N., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.84, no.2, pp.627-631, 1999 (SCI-Expanded, Scopus)

328. Çocukluk döneminde santral diyabetes insipidusun etyolojik değerlendirilmesi

Yavuz T., DARENDELİLER F. F., Şükür M., Minareci K. Ö., BAŞ F., BUNDAK R., et al.

KLİNİK GELİŞİM , vol.12, pp.803-807, 1999 (Peer-Reviewed Journal) Sustainable Development

329. Yenidoğan döneminde BCG aşısı yapılmış okul öncesi dönemdeki çocukların tüberkulin reaksiyonları

GÖKÇAY G., PARTALCI A., Neyzi O., BAŞ F.

Klinik Gelişim , vol.11, pp.663-667, 1998 (Peer-Reviewed Journal) Sustainable Development

330. Kriptorşidik çocuklarda farklı iki human korionik gonadotropin (hCG) tedavi protokolünün karşılaştırılması

ERMİŞ B., BUNDAK R., BAŞ F., BONEVAL C., DARENDELİLER F. F., SAKA H. N., et al.

KLİNİK GELİŞİM , vol.10, pp.267-271, 1997 (Peer-Reviewed Journal)

331. Successful therapy with 3,5,3'-triiodothyroacetic acid (TRIAC) in pituitary resistance to thyroid hormone

Darendeliler F. F., Bas F.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.10, no.5, pp.535-538, 1997 (SCI-Expanded, Scopus)

332. Brachymetacarpia V in familial short stature

Sukur M., Darendeliler F. F., Bundak R., Bas F., Saka N., Gunoz H.

ANNALS OF HUMAN BIOLOGY , vol.24, no.4, pp.371-375, 1997 (SCI-Expanded, Scopus)

333. İnsuline bağımlı diyabetli çocuk ve adolesanlarda metabolik kontrolün diğer parametrelerle ilişkisi

GARİPAĞAOĞLU M., Saka H. N., Hissever H., DARENDELİLER F. F., BUNDAK R., BAŞ F., et al.

Endokrinolojide Yönelişler Dergisi , vol.6, no.4, pp.150-154, 1997 (Peer-Reviewed Journal) Sustainable Development

334. Long-term diazoxide treatment in persistent hyperinsulinemic hypoglycemia of infancy: A patient report

Darendeliler F. F., Bundak R., Bas F., Saka N., Gunoz H.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.10, no.1, pp.79-81, 1997 (SCI-Expanded, Scopus)

335. Çocuk yaş grubunda hastaneye yatan alt solunum yolu infeksiyonlarında prognozu etkileyen faktörler

Partalcı A., BAŞ F., GÖKÇAY G., BULUT A., NALBANT H., NEYZİ O.

ÇOCUK SAĞLIĞI VE HASTALIKLARI DERGİSİ , vol.39, pp.113-120, 1996 (Scopus)

336. spironolactone therapy in hypertrichosis

DARENDELILER F. F., BAŞ F., BALABAN S., BUNDAK R., Demirkol D., SAKA N., et al.

European Journal of Endocrinology , vol.135, no.5, pp.604-608, 1996 (SCI-Expanded, Scopus)

337. Çocuklarda böbrek yetersizliğinde akut periton diyalizi

Karaböcüoğlu M., BAŞ F., Öney V., Nayır A., UĞUR S., UZEL N.

KLİNİK GELİŞİM , vol.8, pp.3512-3535, 1995 (Peer-Reviewed Journal)

338. Çocuklarda status epilepticus

KARABÖCÜOĞLU M., BAŞ F., ÇALIŞKAN M., UĞUR S., UZEL N.

KLİNİK GELİŞİM , vol.7, pp.3345-3347, 1994 (Peer-Reviewed Journal)

339. Bir olgu nedeni ile nörofibromatoz tip I ve renovasküler hipertansiyon

BAŞ F., Alpay H., NAYIR A., EMRE S., TANMAN F., ŞİRİN A.

Istanbul Çocuk Kliniği Dergisi , vol.29, pp.240-243, 1994 (Peer-Reviewed Journal)

340. Atnalı böbrek anomalisi ile birlikte rastlanan diğer bulgular

BAŞ F., ALPAY H., NAYIR A., EMRE S., ŞİRİN A., Kadıoğlu A., et al.

İstanbul Çocuk Kliniği Dergisi , vol.29, pp.136-139, 1994 (Peer-Reviewed Journal)

341. THYROID ULTRASOUND IN IDDM

DARENDELILER F. F., Kadıoğlu A., BAS F., BUNDAK R., Günöz H., Saka N., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY , vol.7, no.1, pp.33-37, 1994 (SCI-Expanded, Scopus) Sustainable Development

342. Ani bebek ölümü sendromu ve uyuma pozisyonu

BAŞ F., GÖKÇAY G., Neyzi O.

KLİNİK GELİŞİM , vol.6, pp.2707-2710, 1993 (Peer-Reviewed Journal)

Papers Presented at Peer-Reviewed Scientific Conferences 268

1. Atypia Of Undetermined Significance (AUS) in Pediatric Thyroid Nodules: Surgery After First Fine Needle Aspiration (FNA) Or Follow-Up?

Yola Atalah Y. E., Vurallı Bakkaloğlu D., Özlük M. Y., İşcan A. Y., Sormaz İ. C., Aksakal N., et al.

Joint Congress Of ESPE and ESE, Kobenhavn, Denmark, 10 - 13 May 2025, pp.1479, (Summary Text)

2. Early Detection of Peripheral and Autonomic Neuropathy in Children And Adolescents With Type 1 Diabetes Mellitus

Yola Atalah Y. E., Taşdemir V., Şirin İnan N. G., Çevikdizici M., Mutlu Ü., Kardelen Al A. D., et al.

Joint Congress of ESPE and ESE, Kobenhavn, Denmark, 10 - 15 May 2025, pp.1479, (Summary Text)

3. Triple a syndrome: phenotypic and genotypic diversity and a novel AAAS gene variant

Sharıfova Mırzayev S., Koç C., Yıldız M., Kardelen Al A. D., Aslanger A. D., Karaman V., et al.

European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025, Kobenhavn, Denmark, 10 - 13 May 2025, pp.174, (Full Text)

4. Pediatrik Tiroid Nodüllerinde Önemi Belirsiz Atipi: İlk İnce İğne Aspirasyon Biyopsisi Sonrası İzlem Mi Operasyon Mu?

Yola Atalah Y. E., Vurallı Bakkaloğlu D., Özlük M. Y., İşcan A. Y., Sormaz İ. C., Aksakal N., et al.

luslararası Katılımlı XXIX. Ulusal Pediatrik Endokrinoloji Ve Diyabet Kongresi, Antalya, Turkey, 15 - 20 April 2025, pp.391, (Summary Text)

5. Tip 1 Diyabet Tanılı Çocuk ve Adölesanlarda Periferik ve Otonomik Nöropatinin Erken Teşhisi

Yola Atalah Y. E., Taşdemir V., Şirin İnan N. G., Çevikdizici M., Mutlu Ü., Kardelen Al A. D., et al.

Uluslararası Katılımlı XXIX. Ulusal Pediatrik Endokrinoloji Ve Diyabet Kongresi, Antalya, Turkey, 15 - 20 April 2025, pp.76, (Summary Text)

6. Pubertal development in hypophosphatemic rickets: does it have an impact on growth?

Kandemir T., Bayrak Demirel Ö., Koç Çalışgan C., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course, Kobenhavn, Denmark, 10 - 13 May 2025, pp.217-218, (Summary Text)

7. Sleep disturbances in adolescents with PCOS: does metabolic status have an impact beyond obesity?

Kandemir T., Yanık H., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., Darendeliler F., et al.

8. Does pubertal induction with transdermal or oral estrogen have an impact on uterine dimensions in Turner syndrome?

Yanık H., Evrüke İ. M., Koç Çalışgan C., Dural Ö., Kardelen Al A. D., Yıldız M., et al.

9. Factors affecting caregiver burden in families of children with type 1 diabetes

Bayrak Demirel Ö., Kandemir T., Koç C., Yanık H., Karaca N., Kardelen Al A. D., et al.

10. Medullary thyroid carcinoma and pathogenic ret proto-oncogene variants in children: clinical outcomes following prophylactic/therapeutic thyroidectomy

Koç C., Yola Atalah Y. E., Yıldız M., Önder S., Yegen G., Aksakal N., et al.

11. Friedreich ataxia and impaired steroidogenesis

Bayrak Demirel Ö., Öney C., Akbaş S., Kandemir T., Aslanger A. D., Kardelen Al A. D., et al.

12. Tıp fakültesi öğrencilerinde nomofobi ve mükemmeliyetçilik ilişkisi.

Yetim Şahin A., Çilesiz B. E., Doğan F. E., Kandemir İ., Tuğrul Aksakal M. Z., Baş F.

9. Ulusal Ergen Sağlığı Kongresi , Diyarbakır, Turkey, 25 - 26 April 2025, pp.40-41, (Full Text)

13. Adolesan dönemde nutrisyon değerlendirmesi.

Tuğrul Aksakal M. Z., Kandemir İ., Sarı M. A., Koçer Z., Sivrikaya T., Güler E., et al.

9. Ulusal Ergen Sağlığı Kongresi, Diyarbakır, Turkey, 25 - 26 April 2025, pp.38-39, (Full Text)

14. Hipofosfatemik Raşitizmli Çocuklarda Ergenlik: Büyüme İçin Kritik Bir Dönem mi?

Kandemir T., Bayrak Demirel Ö., Koç Çalışgan C., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

XXIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi’, Antalya, Turkey, 15 - 20 April 2025, pp.256, (Summary Text)

15. Noonan Sendromlu Çocuklarda Kemik Sağlığı: Büyüme ve Hormonal Faktörlerin Rolü

Kandemir T., Yanık H., Sharıfova Mırzayev S., Aslanger A. D., Kardelen Al A. D., Yıldız M., et al.

XXIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi’, Antalya, Turkey, 15 - 20 April 2025, pp.262, (Summary Text)

16. Polikistik Over Sendromu Tanılı Adolesanlarda Uyku Bozuklukları: Metabolik Durum İle Obeziteden Bağımsız Olarak İlişkili Mi?

Kandemir T., Yanık H., Kardelen Al A. D., Yıldız M., Darendeliler F., Baş F.

XXIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi’, Antalya, Turkey, 15 - 20 April 2025, pp.224, (Summary Text)

17. Büyüme Hormonu Eksikliği Tedavisinde Yeni Bir Alternatif: Haftalık Uygulanan Somatrogon ile Kısa Dönem Sonuçlar

Koç C., Baş F.

47.Pediatri Günleri, İstanbul, Turkey, 9 - 11 April 2025, pp.87-88, (Full Text)

18. Klasik Tip Konjenital Adrenal Hiperplazi Olgularında Alternatif Tedavi Yaklaşımlarının Erişkin Boy Üzerine Etkisi

Sharıfova Mırzayev S., Yanık H., Koç Çalışgan C., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

XXIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 15 - 20 April 2025, pp.67, (Summary Text)

19. Tip 1 Diyabetli Ergenlerde Diyabete Özgü Beslenme Bilgi Düzeyi ve İlişkili Faktörler

ELİUZ TİPİCİ B., Irmak F. N., Aslan Culum A., BAŞ F.

Uluslararası Katılımlı XXIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi XXIII. Diyabet Ekibi Kursu, Antalya, Turkey, 15 April 2025, pp.37-38, (Summary Text)

20. Devlet Destekli Sürekli Glukoz İzlem Cihazı Kullanımında Kan Şekeri İzlem Verilerinin Paylaşılmamasının Metabolik Kontrol Ve Hipoglisemi Korkusu Üzerine Etkisi

Yola Atalah Y. E., Tercan U., Sharıfova Mırzayev S., Koç Çalışgan C., Kardelen Al A. D., Yıldız M., et al.

5. Diyabet Teknolojileri Sempozyumu, İzmir, Turkey, 6 - 07 December 2024, pp.56, (Summary Text)

21. Hipoglisemiden Hiperglisemiye: ABCC8 Gen Varyantlarının Klinik ile İlişkisi

Koç C., Yücesoy M. A., Durmaz D., Aslanger A. D., Kardelen Al A. D., Yıldız M., et al.

6.Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 13 - 15 February 2025, pp.1, (Summary Text)

22. Antley-Bixler sendromlu iki kardeşte POR geninde yeni bir varyant

Karaman V., Bayrak Demirel Ö., Özden S. T., Aslanger A. D., Yıldız M., Poyrazoğlu Ş., et al.

6. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 13 - 15 February 2025, pp.75, (Full Text)

23. Friedreich Ataksisi ve Steroidogenez Bozuklukları

Bayrak Demirel Ö., Öney Yılmaz C., Akbaş S., Kandemir T., Aslanger A. D., Kardelen Al A. D., et al.

6. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 13 - 15 February 2025, pp.75-76, (Summary Text)

24. Parsiyel Androjen Reseptör Kusurunda Nadir Genetik Varyantlar

Kandemir T., Aslanger A. D., Karaman V., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

6. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 13 - 15 February 2025, pp.87, (Full Text)

25. Pubertal Virilizasyon ile Prezente Olan Bir Olguda NR5A1 Gen Delesyonuna Bağlı 46,XY Cinsiyet Gelişim Farklılığı

Bayrak Demirel Ö., Yola Atalah Y. E., Sharıfova Mırzayev S., Aslanger A. D., Karaman V., Kardelen Al A. D., et al.

12. Çocuk Endokrinolojisi Olgu Sunumları Sempozyumu, Ankara, Turkey, 2 - 03 November 2024, pp.50, (Summary Text)

26. Tip 1 Diyabetli Çocuk ve Adolesanlarda Sürekli Glukoz Izleminin Uyku Kalitesi Üzerine Etkisi

Kandemir T., Yanık H., Koç C., Bayrak Demirel Ö., Karaca N., Kardelen Al A. D., et al.

5.Diyabet Teknolojileri Sempozyumu, İzmir, Turkey, 6 - 07 December 2024, pp.23, (Summary Text)

27. Mikrosefali, Epilepsi ve Diyabet Sendromu (MEDS) Olgusunda Yeni Bir Klinik Prezentasyon Şekli: Neonatal Hiperinsülinemik Hipoglisemi

Yola Atalah Y. E., Yanık H., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., Darendeliler F. F., et al.

12. Çocuk Endokrinolojisi Olgu Sunumları Sempozyumu, İzmir, Turkey, 2 - 03 November 2024, pp.212, (Summary Text)

28. Step-by-Step Genetic Insight into a Case of Growth Retardation

Tekin A., TOKSOY G., KINA B. G., ASLANGER A. D., KARAMAN B., SELÇUK B. Ş., et al.

57th Conference of the European-Society-of-Human-Genetics (ESHG), Berlin, Germany, 1 - 04 June 2024, vol.32, pp.1559, (Summary Text)

29. Investigation of Pituitary Function in Langerhans Cell Histiocytosis: A Comprehensive Analysis of Clinical and Radiological Findings

KOÇ ÇALIŞGAN C., TUĞCU D., İRKİN D., KARDELEN AL A. D., ÜNÜVAR A., KARAKAŞ Z., et al.

62nd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), England, 16 - 18 November 2024, (Full Text)

30. Investigation of Pituitary Function in Langerhans Cell Histiocytosis: Comprehensive Analysis of Clinical and Radiological Findings

Koç C., Tuğcu D., İrkin D., Kardelen Al A. D., Ünüvar A., Karakaş Z., et al.

ESPE The 62nd Annual Meeting, Liverpool, England, 16 - 18 November 2024, pp.131-132, (Summary Text)

31. Frasier syndrome with 46,XY gonadal dysgenesis diagnosed during etiological evaluation of nephrotic syndrome: A case report

Yanık H., Koç C., Sönmez F., Uyanık B., Kardelen Al A. D., Yıldız M., et al.

62nd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Liverpool, England, 16 - 18 November 2024, pp.456-457, (Summary Text)

32. Evaluation of metabolic syndrome risk using metabolic syndrome z-score in Bardet-Biedl Syndrome patients with various genotypes

Kandemir T., Tercan U., Bayrak Demirel Ö., Yıldırım B. T., Karaman V., Kardelen Al A. D., et al.

62nd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Liverpool, England, 16 - 18 November 2024, pp.385, (Summary Text)

33. Clinical and molecular characteristics of 26 patients with P450 oxidoreductase deficiency: A multicenter study

Yıldız M., Bayrak Demirel Ö., Çayır A., Ünal E., Aslanger A. D., Kaygusuz S. B., et al.

62nd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Liverpool, England, 16 - 18 November 2024, pp.477-478, (Summary Text)

34. Diagnosis of Cushing’s Disease with DesmopressinInduced Bilateral Inferior Petrosal Sinus Sampling: A Case Report

Bayrak Demirel Ö., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., Baş F., Darendeliler F.

62nd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Liverpool, England, 16 - 18 November 2024, vol.97, pp.324-325, (Summary Text)

35. Students in Turkey show a continuing positive secular change of height but a worrying increase of overweight in males

Bayrak Demirel Ö., Koç C., Şükür N. M., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

62nd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Liverpool, England, 16 - 18 November 2024, pp.408-409, (Summary Text)

36. Investigating the Effects of Familial Mediterranean Fever on Growth and Puberty: Does the Duration of Puberty Change?

Bayrak Demirel Ö., Arık S. D., Kandemir T., Akgün Ö., Kardelen Al A. D., Yıldız M., et al.

62nd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Liverpool, England, 16 - 18 November 2024, vol.97, no.12, pp.145-146, (Summary Text)

37. Early assessment of 24-hour ambulatory blood pressure and arterial stiffness in children with type 1 diabetes mellitus to protect vascular health

Eryılmaz C. C., YILDIZ M., BAKIR KAYI A., Özbaba İ., KARPUZOĞLU F. H., AKSU B., et al.

50th Annual Conference ISPAD 2024, Lizbon, Portugal, 16 - 19 October 2024, (Full Text)

38. Evaluation of bone health in patients diagnosed with juvenile idiopathic arthritis

Çakıroğlu Ü., Akgün Ö., Arık S. D., Eliuz Tipici B., Baş F., Aktay Ayaz N.

31st European Paediatric Rheumatology Congress, Gothenburg, Sweden, 11 - 14 September 2024, vol.22, no.83, pp.8-9, (Summary Text)

39. Rare causes of osteogenesis imperfecta: a cross-sectional study of skeletal features and treatment response in a Turkish cohort

KARDELEN AL A. D., DEMİR K., ÖZTÜRK A. P., ASLANGER A. D., GÜLEÇ Ç., TUNA İNCE E. B., et al.

11th International Conference on Children’s Bone Health (ICCBH) 2024, Salzburg, Austria, 22 - 25 June 2024, pp.370-372, (Summary Text)

40. Tip 1 Diyabetli Çocuk Ve Ergenlerde Tanı Sırasında Otoimmünite ve HLA-DR3/DR4 İlişkisi

Yola Atalah Y. E., Saruhan Direskeneli G., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., Baş F., et al.

Uluslararası Katılımlı XXVIII. Ulusal Pediatrik Endokrinoloji Ve Diyabet Kongresi, Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.85, (Summary Text)

41. Two cases of HDR syndrome due to a large deletion in the 10p15.3p14 region

Memiş G., Arslan H. K., Akbaş S., Aslanger A. D., Yeşil Sayın G., Yavuz S., et al.

European Human Genetics Conference 2024, Berlin, Germany, 1 - 04 June 2024, pp.1, (Summary Text)

42. Investigation of the genetic etiology of short stature

Candan B. Ö., Toksoy G., Aslanger A. D., Baş F., Al A. K., Karaman B.

European Human Genetics Conference, Berlin, Germany, 1 - 04 June 2024, pp.1, (Full Text)

43. Step-by-Step Genetic Insight into a Case of Growth Retardation (POSTER ID P13.067.A)

Tekin A., Toksoy G., Kına B. G., Karaman B., Özsait Selçuk B. Ş., Güleç Ç., et al.

European Society of Human Genetics Congress 2024, Berlin, Germany, 01 June 2024, (Summary Text)

44. Identification of genetic etiology in 130 patients with congenital hypopituitarism

Yavaş Abalı Z., Toksoy G., Baş F., Güran T., Öztürk A. P., Karaman V., et al.

European Human Genetics Conference, Berlin, Germany, 1 - 04 June 2024, pp.1, (Full Text)

45. Identification of genetic etiology in 130 patients with congenital hypopituitarism (POSTER ID P05.050.B)

YAVAŞ ABALI Z., TOKSOY G., BAŞ F., GÜRAN T., ÖZTÜRK A. P., KARAMAN V., et al.

European of Society of Human Genetics Congress 2024, Berlin, Germany, 01 June 2024, (Summary Text)

46. PNPLA3-rs738409 and TM6SF2-rs58542926 missense variants are associated with laboratory parameters in obese adolescents.

KHUDİYEVA S., OYACI Y., YETİM ŞAHİN A., BAŞ F., SAYIN S., KANDEMİR İ., et al.

European Human Genetics Conference, Berlin, Germany, 01 June 2024, (Full Text)

47. Differentiating Pefld type 3 from MAFLD: Is it about genetics?

KHUDİYEVA S., OYACI Y., YETİM ŞAHİN A., BAŞ F., SAYIN S., KANDEMİR İ., et al.

ESPGHAN 56th Annual Meeting, Italy, 15 May 2024, (Full Text)

48. TÜRK ÇOCUKLARINDA NIHAİ BOYUN GÜNCEL DEĞERLENDİRMESİ: “YÜZYILIN EĞILIMI” ÜZERINE ÖN ÇALIŞMA

Bayrak Demirel Ö., Koç C., Şükür N. M., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

28. ULUSAL PEDİATRİK ENDOKRİNOLOJİ KONGRESİ, Girne, Cyprus (Kktc), 30 April - 05 May 2024, vol.1, pp.96-97, (Summary Text)

49. DESMOPRESSIN UYARILI BILATERAL INFERIOR PETROSAL SINÜS ÖRNEKLEMESI ILE CUSHING HASTALIĞI TANISI: OLGU SUNUMU

Bayrak Demirel Ö., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., Baş F., Darendeliler F.

28. ULUSAL PEDİATRİK ENDOKRİNOLOJİ KONGRESİ, Girne, Cyprus (Kktc), 30 April - 05 May 2024, vol.1, pp.280-281, (Summary Text)

50. NADIR RASTLANILAN BARDET BIEDL SENDROMU TANILI OLGULARIN GENETIK, ENDOKRINOLOJIK VE METABOLIK ÖZELLIKLERI

Kandemir T., Tercan U., Bayrak Demirel Ö., Yıldırım B. T., Kardelen Al A. D., Aslanger A. D., et al.

XXVIII. ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Girne, Cyprus (Kktc), 2 - 05 May 2024, pp.200-201, (Summary Text)

51. AILEVI AKDENIZ ATEŞININ BÜYÜME VE ERGENLIK ÜZERINE ETKILERININ ARAŞTIRILMASI: ERGENLIK SÜRESI DEĞIŞIYOR MU?

Bayrak Demirel Ö., Arık S. D., Kandemir T., Akgün Ö., Kardelen Al A. D., Yıldız M., et al.

28. ULUSAL PEDİATRİK ENDOKRİNOLOJİ KONGRESİ, Girne, Cyprus (Kktc), 30 April - 05 May 2024, vol.1, pp.327-328, (Summary Text)

52. TIP 1 DIYABETLI ADOLESANDA TIROTOKSIK HIPOKALEMIK PERIYODIK PARALIZI

Koç C., Bayrak Demirel Ö., Tercan U., Abalı S., Kardelen Al A. D., Yıldız M., et al.

28. ULUSAL PEDİATRİK ENDOKRİNOLOJİ KONGRESİ, Girne, Cyprus (Kktc), 30 April - 05 May 2024, vol.1, pp.264, (Summary Text)

53. Evaluation of Microvascular Disorder and Metabolic Status with Nail Bed Capillaroscopy in Non-Syndromic Early-Onset Morbidly Obese Children

Tercan U., Akgün Ö., Kandemir T., Kardelen Al A. D., Yıldız M., Aktay Ayaz N., et al.

XXVIII. ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Girne, Cyprus (Kktc), 2 - 05 May 2024, pp.107-108, (Summary Text)

54. Menstrual cycle patterns and dysmenorrhea frequency in adolescent girls with familial Mediterranean fever: Cross-Sectional case-control study.

Demirkan F. G., Yetim Şahin A., Çakmak F., Akgün Ö., Guliyeva V., Tuğrul Aksakal M. Z., et al.

2nd Familial Mediterrean Fever Meeting, İstanbul, Turkey, 3 - 05 May 2024, pp.10-11, (Full Text)

55. Obez Ergenlerde Alkolik Olmayan Karaciğer Yağlanmasında Genetik ve Epigenetik Değişikliklerin Araştırılması

Khudiyeva S., oYACI Y., YETİM ŞAHİN A., BAŞ F., Sayın S., KANDEMİR İ., et al.

46. Pediatri Günleri Geçmişten geleceğe hep birlikte el ele, Turkey, 16 - 18 April 2024, (Summary Text)

56. KRONİK BÖBREK YETMEZLİĞİ OLAN TÜRK ERGENLERDE SORUNLAR, BAŞA ÇIKMA TARZLARI VE TERCİH EDILEN ÇEVRİMİÇİ AKTİVİTENİN DEPRESYON, ANKSİYETE VE DİĞER PSİKOLOJİK BOZUKLUKLARLA İLİŞKİSİ

KANDEMİR İ., GÜDEK K., YETİM ŞAHİN A., Tuğrul Aksakal M., YÜRÜK YILDIRIM Z. N., YILMAZ A., et al.

46. Pediatri Günleri Geçmişten geleceğe hep birlikte el ele, Turkey, 16 - 18 April 2024, (Summary Text)

57. Klinik ve Laboratuvar Özellikleri ile Otoimmun Poliglandüler Tip 1 Tanılı Hastaların Değerlendirilmesi: Olgu serisi

Tercan U., Yıldız M., Poyrazoğlu Ş., Baş F., Darendediler F.

26. Ulusal Pediatrik Endokrinoloji Kongresi, Antalya, Turkey, 26 - 30 October 2022, pp.340-341, (Summary Text)

58. Effects of Regular Well-Child Follow Up From Birth on Adolescent Wellbeing: Preliminary Results

TUĞRUL AKSAKAL M. Z., ÖZBÖRÜ AŞKAN Ö., BAKIR KAYI A., YETİM ŞAHİN A., KESKİNDEMİRCİ G., Kuleli O., et al.

3. Uluslararası Sosyal Pediatri Kongresi, İzmir, Turkey, 16 November 2022, (Summary Text)

59. Do Athlete Girls Eat Healthy?

Eliuz Tipici B., Erdoğan F. N., Tuğrul Aksakal M. Z., Ketenci Altıkardeşler Ö., Yakal S., Yetim Şahin A., et al.

67. Türkiye Milli Pediatri Kongresi, Girne, Cyprus (Kktc), 18 - 22 October 2023, pp.361-362, (Summary Text)

60. INVESTIGATION OF SHOX GENE MUTATIONS

Candan B. Ö., Aslanger A. D., Özsait Selçuk B. Ş., Bulut G., Toksoy G., Baş F., et al.

14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Macedonia, 5 - 07 October 2023, pp.91, (Summary Text)

61. A Rare Diagnosis in a Virilized Adolescent with a 46,XX Karyotype- Gonadoblastoma with Dysgerminoma

KANDEMİR T., KARAKILIÇ ÖZTURAN E., DURAL Ö., BALCI E. İ., BAYRAM A., ÖNDER S., et al.

61ST ANNUAL MEETİNG OF THE EUROPEAN SOCİETY FOR PAEDİATRİC ENDOCRİNOLOGY (ESPE), The Hague, Netherlands, 21 - 23 September 2023, (Summary Text)

62. Nailfold capillaroscopy: An alternative non-invasive tool for evaluating microvascular involvement in children with type 1 diabetes

ÇAKMAK F., İNAN BALCI E., YILDIZ M., DEMİRKAN F. G., YETİM ŞAHİN A., POYRAZOĞLU Ş., et al.

61st European Society for Paediatric Endocrinology (ESPE) Annual Meeting, Netherlands, 21 - 23 September 2023, (Summary Text) Sustainable Development

63. A Rare Coexistence of Turner Syndrome and Mycosis Fungoides: A Case Report

Bayrak Demirel Ö., Karakılıç Özturan E., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., Baş F., et al.

61st Annual ESPE Meeting 2023, The Hague, Netherlands, 21 - 23 September 2023, (Unpublished)

64. Diagnostic Journey with an 80-gene Panel in Non-syndromic Early-Onset Severe Obesity: Association of Outcomes with Metabolic Status and Hyperphagia

Tercan U., Yıldız M., Aslanger A. D., Kardelen Al A. D., Poyrazoğlu Ş., Baş F., et al.

61st Annual ESPE (ESPE 2023), The Hague, Netherlands, 21 - 23 September 2023, pp.243-244, (Full Text) Sustainable Development

65. Investigation of Genetic Etiology of Short Stature

Karaman B., Najaflı A., Baş F., Darendeliler F. F.

14th European Cytogenomics Conference , Montpellier, France, 1 - 04 July 2023, pp.50, (Summary Text) Sustainable Development

66. TİP 1 Diyabetli Çocuklarda Non-invaziv Bir Yöntem Olan Tırnak Yatağı Kapilleroskopisi ile Mikrovasküler Etkilenmenin Değerlendirilmesi

Çakmak F., İnan Balcı E., Yıldız M., Demirkan F. G., Yetim Şahin A., Poyrazoğlu Ş., et al.

XXVII.ULUSAL PEDİATRİK ENDOKRİNOLOJİ ve DİYABET KONGRESİ, Antalya, Turkey, 2 - 07 May 2023, pp.115, (Summary Text)

67. Course of Papillary Thyroid Carcinoma Diagnosed in Childhood and Adolescence and Followed Through Adulthood: Experience from a Tertiary Referral Center

Hacişahinoğulları H., İnan Balcı E., Yenidünya Yalın G., Soyluk Selçukbiricik Ö., Baş F., Kubat Üzüm A., et al.

25 th European Congress of Endocrinology - ECE 2023, İstanbul, Turkey, 13 - 16 May 2023, pp.1-3, (Summary Text)

68. Transfer Of Congenital Adrenal Hyperplasia Patients From The Pediatric ClinicTo The Adult Clinic: A Single Center Experience

Bilik Oyman G., Kandemir T., Hacişahinoğulları H., Yenidünya Yalın G., Yıldız M., Gül N., et al.

25 th European Congress of Endocrinology - ECE 2023, İstanbul, Turkey, 13 - 16 May 2023, pp.1-3, (Summary Text)

69. Turner Sendromu İle Mikozis Fungoides Birlikteliği: Nadir Bir Olgu Sunumu

BAYRAK DEMİREL Ö., KARAKILIÇ ÖZTURAN E., KARDELEN AL A. D., YILDIZ M., POYRAZOĞLU Ş., BAŞ F., et al.

XXVII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 2 - 07 May 2023, (Summary Text)

70. Çocukluk Döneminde Tanı Alan Papiller Tiroid Karsinomu Hastalarının Erişkin Dönem Seyrinin Değerlendirilmesi

İnan Balcı E., Bayrak Demirel Ö., Hacışahinoğulları H., Yenidünya Yalın G., Soyluk Selçukbiricik Ö., Kubat Üzüm A., et al.

XXVII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 4 - 07 May 2023, vol.1, no.1, pp.134, (Summary Text)

71. Transition from childhood to adult care in type 1 diabetes mellitus: Single-center experience

YİĞİT YALÇIN B., TERCAN U., YILDIZ M., HACİŞAHİNOĞULLARI H., YENİDÜNYA YALIN G., GÜL N., et al.

25th European Congress of Endocrinology, İstanbul, Turkey, 13 May 2023, vol.90, pp.169, (Summary Text)

72. Boy Kısalığı ve Kiloda Artış Şikayetleri ile Başvuran Bir Hastada Saptanan Cushing Hastalığı

TUNCAY H. A., AYSAL B., KANDEMİR T., BAYRAK DEMİREL Ö., TERCAN U., KARDELEN AL A. D., et al.

45. Pediatri Günleri / 24. Pediatri Hemşireliği Günleri / 1. Pediatri Diyetisyenliği Günleri, İstanbul, Turkey, 25 - 28 April 2023, (Summary Text)

73. NOONAN SENDROMU : OLGU SUNUMU

Tırtır Yılmaz B., Kandemir T., Aslanger A. D., Yıldız M., Poyrazoğlu Ş., Baş F., et al.

45. Pediatri Günleri, İstanbul, Turkey, 25 - 28 April 2023, (Unpublished)

74. Comparison of Indices Used to Determine Obesity-Related Fatty Liver in Adolescents

Yetim Şahin A., Tuğrul Aksakal M. Z., Bulakçı M., Baş F.

45. Pediatri Günleri, İstanbul, Turkey, 25 - 28 April 2023, pp.10-11, (Summary Text)

75. Ergen Sporcularda Akıllı Telefon Bağımlılığı Düzeyi ve Uyku Üzerindeki Etkileri

Ketenci Altıkardeşler Ö., Yetim Şahin A., Tuğrul Aksakal M. Z., Baş F.

45.Pediatri Günleri, İstanbul, Turkey, 25 - 28 April 2023, pp.1-2, (Summary Text)

76. Konjenital Adrenal Hiperplazi Yenidoğan Taraması 2022 Sonuçları: Tek Merkez Deneyimi

Yavuz R., Kandemir T., Bayrak Demirel Ö., Tercan U., İnan Balcı E., Kardelen Al A. D., et al.

45. Pediatri Günleri / 24. Pediatri Hemşireliği Günleri / 1. Pediatri Diyetisyenliği Günleri, İstanbul, Türkiye, 25 - 28 Nisan 2023, İstanbul, Turkey, 25 - 28 April 2023, pp.408-409, (Summary Text)

77. Diyabetes Mellitusla Seyreden Nadir Bir Genodermatoz Nedeni: H Sendromu

Yaman B., Tercan U., Bayrak Demirel Ö., Kandemir T., Kardelen Al A. D., Yıldız M., et al.

45. PEDİATRİ GÜNLERİ, İstanbul, Turkey, 25 - 28 April 2023, pp.530-531, (Summary Text)

78. Evaluation of Genetic Etiology in Children Born Small for Gestational Age with Persistent Short Stature

ÖZTÜRK A. P., ASLANGER A. D., KARAKILIÇ ÖZTURAN E., KONUR E. N., GÜLEÇ Ç., KARAMAN V., et al.

60th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Roma, Italy, 15 - 17 September 2022, pp.313, (Summary Text)

79. Osteogenezis Imperfekta Tanılı 15 Olgunun Moleküler Sonuçları

Hacer Ö., Aslanger A. D., Kalaycı T., Güleç Ç., Demir K., Toksoy G., et al.

15. Ulusal Tıbbi Genetik Kongresi, Muğla, Turkey, 09 November 2022, pp.149, (Summary Text)

80. Gebelik Haftasına Göre Küçük Doğan (Sga) Çocuklarda Sebat Eden Boy Kısalığının Etiyolojisinin Genetik Analizler Ile Değerlendirilmesi

Karaman V., Aslanger A. D., Konur E. N., Öztürk A. P., Toksoy G., Özsait Selçuk B. Ş., et al.

15.ULUSLARARASI KATILIMLI, ULUSAL TIBBİ GENETİK KONGRESİ, Muğla, Turkey, 9 - 13 November 2022, pp.189, (Summary Text)

81. Metabolik Hastalıklarda Endokrinolojik Sorunlar; Biz ne yapabiliriz ?

İnan Balcı E., Balcı M. C., Karakılıç Özturan E., Yıldız M., Poyrazoğlu Ş., Baş F., et al.

XXVI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 26 October - 30 November 2022, pp.91, (Full Text)

82. Papillary Tyhroid Carcinoma in Two Siblings With Congenital Famial Hypothyroidism

İnan Balcı E., Yıldız M., Poyrazoğlu Ş., Baş F., Darendeliler F. F.

60 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) Rome , Rome, Italy, 15 - 17 September 2022, pp.571-572, (Full Text)

83. Investigation of Genes Associated with Multiple Pituitary Hormone Deficiencies via Next Generation Sequencing Technology

ÖZTÜRK A. P., TOKSOY G., BAŞ F., YAVAŞ ABALI Z., Bagirova G., KARAMAN V., et al.

60th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Roma, Italy, 15 September 2022, (Full Text)

84. Ağır Boy Kısalığı Olan Olgumuzda Cornelia de Lange Sendromu ve IGFR1 kusuru birlikteliği

İNAN BALCI E., ASLANGER A. D., KARAKILIÇ ÖZTURAN E., YILDIZ M., POYRAZOĞLU Ş., BAŞ F., et al.

11. Çocuk Endokrinolojisi Olgu sunumları, Turkey, 13 May 2022, pp.68, (Summary Text)

85. SENDROMİK BÜYÜME GELİŞME GERİLİĞİNİN NADİR BİR NEDENİ: 1q21.1 DUPLİKASYON SENDROMU

ASLANGER A. D., ÖZTÜRK A. P., BAŞ F., KARAMAN B.

ÇOCUK ENDOKRİNOLOJİSİ OLGU SUNUMLARI -11-, Turkey, 13 May 2022, pp.67, (Summary Text)

86. ERKEN ERGENLİK İLE RATHKE KLEFT KİSTİ BİRLİKTELİĞİ

Bayrak Demirel Ö., Yıldız M., Poyrazoğlu Ş., Baş F., Darendeliler F. F.

11. OLGU SUNUMLARI SEMPOZYUMU, İstanbul, Turkey, 13 May - 14 October 2022, (Unpublished)

87. COVID-19 INFECTION IN CHILDREN WITH CANCER AFTER THE FIRST WAVE IN TURKEY: A STUDY OF THE TURKISH PEDIATRIC ONCOLOGY (TPOG) AND HEMATOLOGY (TPHD) SOCIETIES

TUĞCU D., ÇÖLLÜ M., TUNA DEVECİ R., BİLİCİ M., BAŞ F., KARAMAN S., et al.

PEDIATRIC BLOOD CANCER;53rd Congress of the International Society of Paediatric Oncology (SIOP) Virtual Congress, Hawaii, United States Of America, 21 - 24 October 2021, vol.68, pp.139-140, (Summary Text) Sustainable Development

88. Hiperprolaktinemi Etiyolojisinde Nadir Bir Neden: 6-Piruvoil-Tetrahidrobiopterin Sentaz (PTPS) Eksikliği

Tercan U., Yıldız M., Selamioğlu A., Karaca M., Poyrazoğlu Ş., Baş F., et al.

25. Ulusal Pediatrik Endokrinoloji Kongresi, Antalya, Turkey, 6 - 10 October 2021, pp.281-282, (Summary Text)

89. Sitokrom P450 oksidoredüktaz eksikliğine bağlı konjenital adrenal hiperplazi hastalarının klinik ve laboratuvar özellikleri: Olgu serisi

Bayrak Demirel Ö., Baş F., Kalaycı T., Yıldız M., Konur E. N., Poyrazoğlu Ş., et al.

25. Ulusal Pediatrik Endokrinoloji Kongresi, Antalya, Turkey, 6 - 10 October 2021, pp.305-307, (Full Text)

90. İdiyopatik Boy Kısalığında Nihai Boy ve Etiyolojiye Yönelik Değerlendirme

Önal Özen İ., Bayrak Demirel Ö., Yıldız M., Poyrazoğlu Ş., Baş F., Darendeliler F. F.

25. Ulusal Pediatrik Endokrinoloji Kongresi, Antalya, Turkey, 6 - 10 October 2021, pp.253-254, (Full Text)

91. Çoğul Hipofiz Hormon Eksikliklerinde İlişkili Genlerin Yeni Nesil Dizileme Teknolojisi İle Araştırılması

ÖZTÜRK A. P., TOKSOY G., BAŞ F., YAVAŞ ABALI Z., KARAMAN V., YILDIZ M., et al.

XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 06 October 2021, (Summary Text)

92. Response to growth hormone therapy with high IGF-1-levels and severe insulin resistance in two-cases with SOFT syndrome: A novel homozygous mutation in POC1A

KARAKILIÇ ÖZTURAN E., ALTUNOĞLU U., ÖZTÜRK A. P., TOKSOY G., TUTKU TURGUT G., POYRAZOĞLU Ş., et al.

59th Annual ESPE (ESPE 2021 Online), 22 - 23 September 2021, vol.94, pp.277, (Summary Text)

93. Evaluation of early puberty in boys and girls with Silver-Russell Syndrome: Discordance between testicular growth and pituitary-gonadal hormones in male cases

YILDIZ M., BAŞ F., KARAMAN B., POYRAZOĞLU Ş., BAŞARAN S., DARENDELİLER F. F.

59th ESPE 2021 Meeting, Turkey, 22 September 2021, (Summary Text)

94. Phenotypic Characteristics of Patients with 45,X/46,XY Mosaicism: Growth, Gonadal Pathology and Tumour Risk.

POYRAZOĞLU Ş., BAŞ F., KARAMAN B., YILDIZ M., BAŞARAN S., DARENDELİLER F. F.

59 th Annual Meeting of the . European Society of Paediatric Endocrinology, 22 September 2021, (Full Text)

95. Folow-up of individuals with gender dyshoria:experience of a pediatric endocrinology clinic in a tertiary center

KARAKILIÇ ÖZTURAN E., ÖZTÜRK A. P., BAŞ F., POYRAZOĞLU Ş., AYAZ A. B., KAPTAN S., et al.

4TH EUROPEAN PROFESSIONAL ASSOCIATION FOR TRANSGENDER HEALTH, Sweden, 11 August 2021, (Full Text)

96. Follow-up of individuals with gender dysphoria: Experience of a pediatric endocrinology clinicin a tertiary center

Karakılıç Özturan E., Öztürk A. P., Baş F., Poyrazoğlu Ş., Ayaz A. B., Kaptan S., et al.

4th EPATH Hybrid Conference: Reconnecting and Redefining Transgender Care, Gothenburg, Sweden, 11 - 13 August 2021, pp.77, (Summary Text)

97. Primer Gonadal Yetmezliğin Etiyolojisinde Yeni ve Nadir Bir Neden: Transaldolaz Eksikliği

YILDIZ M., ÖNAL Z., SARBAN E., KABİL T. G., ASLANGER A. D., YEŞİL SAYIN G., et al.

10. Çocuk Endokrinolojisi Olgu, Turkey, 09 April 2021, pp.73, (Summary Text)

98. PRİMER GONADAL YETMEZLİĞİN ETİYOLOJİSİNDE YENİ VENADİR BİR NEDEN: TRANSALDOLAZ EKSİKLİĞİ

Yıldız M., Önal Z., Sarban E., Kabil T. G., Aslanger A., Yeşil G., et al.

Çocuk endokrinolojisi olgu sunumları-10, İzmir, Turkey, 09 April 2021, pp.73, (Summary Text)

99. NÖROBLASTOM TANILI HASTADA ERKEN PUBERTE İLE TANI ALAN KONJENİTAL ADRENAL HİPERPLAZİ OLGUSU

SARBAN E., YILDIZ M., ÖZTÜRK A. P., KARAMAN S., YEŞİL G., POYRAZOĞLU Ş., et al.

Çocuk endokrinolojisi olgu sunumları-10, İzmir, Turkey, 09 April 2021, (Summary Text)

100. BOY KISALIĞI İLE BAŞVURAN BİR OLGUDA AYIRICI TANI: İDİYOPATİK BOY KISALIĞI GERÇEK TANI MI?

KARAKILIÇ ÖZTURAN E., ÖZTÜRK A. P., ASLANGER A., YEŞİL G., SARBAN E., YILDIZ M., et al.

Çocuk endokrinolojisi olgu sunumları-10, İzmir, Turkey, 09 April 2021, (Summary Text)

101. Boy kısalığı ile başvuran bir olguda ayırıcı tanı: İdiyopatik boy kısalığı gerçek tanı mı

KARAKILIÇ ÖZTURAN E., ÖZTÜRK A. P., ASLANGER A. D., YEŞİL SAYIN G., SARBAN E., YILDIZ M., et al.

10. Çocuk Endokrinolojisi Olgu sunumları, Turkey, 09 April 2021, pp.119, (Summary Text)

102. TBX19 mutasyonuna bağlı konjenital izole ACTH eksikliği ile beraber sekonder hipotirodi, BH eksikliği ve hiper IgE benzeri sendrom birlikteliği

ÖZTÜRK A. P., YÜCEL E., SABAN E., KARAKILIÇ ÖZTURAN E., ASLANGER A. D., YEŞİL SAYIN G., et al.

10. Çocuk Endokrinolojisi Olgu sunumları, Turkey, 09 April 2021, pp.110, (Summary Text)

103. OSTEOGENEZİS İMPERFEKTA TANILI HASTALARDA BÜYÜME VE PUBERTE

Öztürk A. P., Dudaklı A., Karakılıç Özturan E., Yıldız M., Poyrazoğlu Ş., Baş F., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrimiçi Kongresi, 30 October - 01 November 2020, (Unpublished)

104. Ailevi Erken Puberte Olgularında MKRN3 ve DLK1 Genlerinin Dizilenmesi

BAŞARAN S., UYGUNER Z. O., BAŞ F., DARENDELİLER F. F., POYRAZOĞLU Ş., KARAKILIÇ ÖZTURAN E.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrimiçi Kongresi, Turkey, 30 October - 03 November 2020, (Full Text)

105. Klasik tip 21 hidroksilaz eksikliğine bağlı konjenital adrenal hiperplazi tanılı olgularda puberte özellikleri, pubertal boy kazanımı ve final boya etki eden faktörlerin değerlendirilmesi: çok merkezli çalışma

YAVAŞ ABALI Z., YILDIZ M., BAŞ F., ÖNAL H., ABALI S., ÇİLSAAT G., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Ankara, Turkey, 30 October 2020, (Summary Text)

106. Her Tip 1 Diyabet tanısı alan hasta Tip1 Diyabet olmayabilir: MODY tanılı hastalarımızın değerlendirilmesi

ÖZBAY D., KARDELEN AL A. D., KARAKILIÇ ÖZTURAN E., ÖZTÜRK A. P., YILDIZ M., POYRAZOĞLU Ş., et al.

XXIV Ulusal Pediatri Endokrinoloji ve Diyabet Kongresi, Çevrim içi, Turkey, 30 October - 01 November 2020, (Summary Text) Sustainable Development

107. Osteogenezis İmperfekta Tanılı Hastalarda Büyüme Ve Puberte

ÖZTÜRK A. P., DUDAKLI A., KARAKILIÇ ÖZTURAN E., KARDELEN AL A. D., YILDIZ M., POYRAZOĞLU Ş., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Ankara, Turkey, 30 October 2020, (Summary Text)

108. Çocukluk çağında nadir bir vaka: Hipofizer jigantizm

UFACIK YÖNDEM A., ÖZTÜRK A. P., KARAKILIÇ ÖZTURAN E., KARDELEN AL A. D., YILDIZ M., POYRAZOĞLU Ş., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Çevrim içi, Turkey, 30 October - 01 November 2020, (Summary Text)

109. Turner Sendromunda önerilen dozda büyüme hormonu tedavisi altında yüksek IGF-1 düzeylerinin değerlendirilmesi: Tedavi yönetimindeki zorluklar

KARAKILIÇ ÖZTURAN E., KARAGÖZ N., KARDELEN AL A. D., ÖZTÜRK A. P., CEYLANER S., POYRAZOĞLU Ş., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Çevrim içi, Turkey, 30 October - 01 November 2020, (Summary Text)

110. Global gelişim geriliği ve boy kısalığı nedeniyle “Kleefstra sendromu 2” tanısı alan hastada daha önce bildirilmeyen diyabet ve büyüme hormonu eksikliği birlikteliği

KARAKILIÇ ÖZTURAN E., ALTUNOĞLU U., ÖZTÜRK A. P., KARDELEN AL A. D., YILDIZ M., POYRAZOĞLU Ş., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Çevrim içi, Turkey, 30 October - 01 November 2020, (Summary Text)

111. Osteogenezis İmperfekta Tanılı Hastalarda Büyüme Ve Puberte

ÖZTÜRK A. P., DUDAKLI A., KARAKILIÇ ÖZTURAN E., KARDELEN AL A. D., YILDIZ M., POYRAZOĞLU Ş., et al.

XXIV Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Çevrim içi, Turkey, 30 October - 01 November 2020, (Summary Text)

112. Silver-Russell Sendromu tanılı kız ve erkek olgularımızda erkence pubertenin değerlendirilmesi ve erkek olgularda testis büyümesi ile hipofizer-gonadal hormonlar arasında uyumsuzluk

Yıldız M., Baş F., Karaman B., Poyrazoğlu Ş., Başaran S., Darendeliler F. F.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Ankara, Turkey, 30 October - 01 November 2020, pp.102, (Summary Text)

113. Nadir bir boy kısalığı nedeni olan SOFT sendromu tanılı olgularımızda çok yüksek IGF1 düzeyleri ve ağır insülin direnci birlikteliği ile büyüme hormonu tedavisine yanıtın değerlendirilmesi

KARAKILIÇ ÖZTURAN E., ALTUNOĞLU U., TOKSOY G., ÖZTÜRK A. P., KARDELEN AL A. D., TURGUT G. T., et al.

XXIV ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Çevrim içi, Turkey, 30 October - 01 November 2020, (Summary Text)

114. SOFT Sendromu Tanılı Olgularımızda Çok Yüksek IGF1 Düzeyleri Ve Ağır İnsülin Direnci Birlikteliği İle Büyüme Hormonu Tedavisine Yanıtın Değerlendirilmesi

Karakılıç Özturan E., Altunoğlu U., Toksoy G., Öztürk A. P., Kardelen Al A. D., Turgut G. T., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrimiçi Kongresi , 30 October - 01 November 2020, pp.1-2, (Summary Text)

115. Global gelişim geriliği ve boy kısalığı olan bir hastada nadir görülen bir sendrom: Kleefstra sendromu 2

Karakılıç Özturan E., Altunoğlu U., Öztürk A. P., Kardelen Al A. D., Yıldız M., Poyrazoğlu Ş., et al.

XXIV.XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrimiçi Kongresi, Ankara, Turkey, 30 October - 01 November 2020, pp.1-2, (Summary Text)

116. Steroid 11 beta-hidroksilaz eksikliği olan 100 çocuk hastanın klinik bulgularının genetik ve adrenokortikal hormon profili ile ilişkisinin değerlendirilmesi

YILDIZ M., IŞIK E., DEMİRCİOĞLU S., KESKİN M., Özbek M. N., BAŞ F., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi, Turkey, 30 October - 01 November 2020, (Summary Text)

117. Ayme-Gripp Sendromu Olan Bir Olguda Büyüme Hormonu Tedavisi

Öztürk A. P., Akkuş N., Karakılıç Özturan E., Yıldız M., Poyrazoğlu Ş., Baş F., et al.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrimiçi Kongresi , 30 October - 01 November 2020, (Unpublished)

118. SUN-077 Do Low Sex Hormone Binding Globulin Levels in Newborns Predict Weight Gain in Infancy and Early Childhood?

Küçükemre Aydın B., Yasa B., P. Moore J., Yasa C., POYRAZOĞLU Ş., BAŞ F., et al.

ENDO 2020 Congress, United States Of America, 28 - 31 March 2020, (Full Text)

119. Çocukluk Çağı Obez ve Erişkin Metabolik Bozuklukları olan Hastalarda Leptin ve Leptin Reseptörü Polimorfizmlerinin Serum Leptin Seviyeleri ile Karşılaştırılması

Akan G., Atalar F., Baş F., Demir G., Tarhan T., Bundak R., et al.

Endokrin Hastalıklar ve Genetik Sempozyumu, Bolu, Turkey, 8 - 10 October 2009, pp.112, (Full Text)

120. Konjenital Adrenal Hiperplazi Vakalarında LEP ve LEPR Gen Polimorfizmlerinin İnsülin Direnci ile İlişkilendirilmesi

BAŞ F., TARHAN T., ATALAR F., AKAN G., Demir G., DARENDELILER F., et al.

XIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, pp.103, (Full Text)

121. PPAR Gamma Gene Expression is Positively Correlated with Leptin and MC4R Expressions in Congenital Adrenal Hyperplasia

ATALAR F., BAŞ F., TARHAN T., AKAN G., DARENDELILER F., BUNDAK R., et al.

50th Annual Meeting of the European Society of Pediatric Endocrinology (ESPE), United Kingdom, pp.172, (Full Text)

122. İdiyopatik Boy Kısalığı Etiyopatogenezinde IGF-1 Gen Polimorfizmi Araştırılması

Tekcan D., Baş F., Atalar F., Akan G., Tarhan T., Darendeliler F.

33. Pediatri Günleri ve 12. Pediatri Hemşireliği Günleri, İstanbul, Turkey, 28 - 31 March 2011, pp.13, (Full Text)

123. “Expression of IGF-1, IGFBP-3, IGF-1R Genes in Idiopathic Short Stature

CENGIZ P., BAŞ F., BUNDAK R., ATALAR F., DARENDELILER F., AYDIN B. K., et al.

49th Annual Meeting of the European Society of Pediatric Endocrinology (ESPE), Czech Republic, pp.198, (Full Text)

124. İdiyopatik Boy Kısalığı Hastalarında IGF-1, IGFBP-3 Düzeyleri ve Gen Ekspresyonlarının İlişkisi

Cengiz P., ATALAR F., BAŞ F., BUNDAK R., DARENDELILER F., AKAN G., et al.

XIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, pp.135, (Full Text)

125. Leptin ve Leptin Reseptör Polimorfizmlerinin Çocukluk Çağı Obezitesi ile İlişkisi

Akan G., Atalar F., Baş F., Demir G., Tarhan T., Darendeliler F., et al.

XIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 17 - 21 November 2009, pp.160, (Full Text)

126. Erken Obezite Tedavisi için Marker olan Pro12ALA Ppar? Ve VAL103ILE MC4R Polimorfizmlerinin Obez Çocuklardaki Sıklıklarının Araştırılması

Demir G., ATALAR F., BAŞ F., AKAN G., TARHAN T., DARENDELILER F., et al.

Endokrin Hastalıklar ve Genetik Sempozyumu, Bolu, Turkey, pp.90, (Full Text) Sustainable Development

127. CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children

ATALAR F., WOLLNIK B., DARENDELILER F., BAŞ F., GÜNÖZ H., KAYSERILI H., et al.

43rd Annual Meeting European Society for Paediatric Endocrinology, Switzerland, pp.109, (Full Text)

128. Correlation of Leptin, Leptin Receptor Gene Polymorphism and Expression with Insulin Resistance in Congenital Adrenal Hyperplasia

BAŞ F., ATALAR F., DARENDELILER F., TARHAN T., AKAN G., AYDIN B. K., et al.

49th Annual Meeting of the European Society of Pediatric Endocrinology (ESPE), Czech Republic, pp.118, (Full Text)

129. “Leptin, Leptin Receptor, MC4R, PPAR Gamma and Osteopontin Gene Polymorphisms in Obese and Overweight Children”

ATALAR F., BAŞ F., AKAN G., TARHAN T., DARENDELILER F., AYDIN B. K., et al.

49th Annual Meeting of the European Society of Pediatric Endocrinology (ESPE), Czech Republic, pp.79, (Full Text)

130. Proinflamatuvar Bir Mediatör Olan Osteopontin ve Obezite

TARHAN T., ATALAR F., BAŞ F., AKAN G., Demir G., DARENDELILER F., et al.

Endokrin Hastalıklar ve Genetik Sempozyumu, Bolu, Turkey, pp.113, (Full Text) Sustainable Development

131. Konjenital Adrenal Hiperplazide Pro12Ala ve Val103 Polimorfizmlerinin İncelenmesi

TARHAN T., ATALAR F., BAŞ F., AKAN G., Demir G., DARENDELILER F., et al.

XIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, pp.124, (Full Text)

132. Çocukluk Çağı Obezitesinde IGF-1 Ve IGFBP-3 Genleri ile Lepin Gen Ekspresyonlarının Korelasyonunun Araştırılması

Atalar F., Baş F., Akan G., Tarhan T., Darendeliler F., Bundak R., et al.

XIV.Ulusal Pediatrik Endokrin ve Diyabet Kongresi, Muğla, Turkey, 4 - 10 October 2010, pp.122, (Full Text)

133. The Crosstalk Between the Insulin-Like Growth Factor (IGF)-IGF Binding Proteins Axis and Leptin: Differential Impact of Childhood Obesity in IGF-1, IGFBP-3 and Leptin

ATALAR F., BAŞ F., AKAN G., TARHAN T., DARENDELILER F., BUNDAK R., et al.

European Society For Paediatric Endocrinology (ESPE), United Kingdom, pp.553, (Full Text) Sustainable Development

134. Leptin Ve Leptin Regülatörlerinin Çocukluk Çağı Obezitesindeki Rollerinin Araştırılması

AKAN G., TARHAN T., ATALAR F., BAŞ F., DARENDELILER F., BUNDAK R., et al.

XIV.Ulusal Pediatrik Endokrin ve Diyabet Kongresi, Muğla, Turkey, pp.207, (Full Text)

135. Genotype-Phenotype Correlation and Clinical Findings in 145 Patients with Congenital Adrenal Hyperplasia: Single Centre Experience

Çilsaat G., Toksoy G., Baş F., Karaman B., Poyrazoğlu Ş., Uyguner Z. O., et al.

58 th Annual Meeting European Society for Paediatric Endocrinology (ESPE), Vienna, Austria, 20 - 22 September 2019, vol.1, no.1, pp.282, (Summary Text) Sustainable Development

136. Cinsiyet Kimlik Hoşnutsuzluğu Olan Adölesan Bireylerin Izlemi: Üçüncü Basamak Bir Merkezin Deneyimi

Karakılıç Özturan E., Öztürk A. P., Kardelen Al A. D., Poyrazoğlu Ş., Baş F., Ayaz A. B., et al.

ADSAD 1. Ulusal Ergen Sağlığı Kongresi, İstanbul, Turkey, 15 - 17 November 2019, pp.46, (Summary Text)

137.

Tuğrul Aksakal M. Z., Yetim Şahin A., Kılıç A., Baş F., Darendeliler F., Gökçay E. G.

ADSAD I. Ulusal Ergen Sağlığı Kongresi, İstanbul, Turkey, 15 - 17 November 2019, pp.52, (Summary Text)

138. **Novel variants in DHH gene identified with 46,XY gonadal dysgenesis**

Aghayev A., Toksoy G., Poyrazoglu Ş., Karaman B., Avci S., Abali Z. Y., et al.

52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 15 - 18 June 2019, pp.1250-1251, (Summary Text)

139. Targeted Panel Gene Sequencing for Identification of Genetic Etiology of 46, XY Disorders of Sex Development

Poyrazoğlu Ş., TOKSOY G., Aghayev A., KARAMAN B., Şahin A., ALTUNOĞLU U., et al.

European Society for Paediatric Endocrinology (ESPE), Basel, Switzerland, 20 - 22 September 2019, pp.193, (Full Text)

140. Two Siblings with Hypophosphatemic Rickets: SLC34A3 Gene Mutations with Different Clinical Phenotypes

KARAKILIÇ ÖZTURAN E., ÖZTÜRK A. P., KARDELEN A. D., POYRAZOĞLU Ş., BAŞ F., DARENDELİLER F. F.

The 58th Annual ESPE Meeting, Viyana, Austria, 19 - 21 September 2019, pp.92, (Full Text)

141. Targeted panel gene sequencing for identification of genetic etiology of 46,XY disorders sex development.

POYRAZOĞLU Ş., TOKSOY G., AGHAYEV A., KARAMAN B., AVCI Ş., ALTUNOĞLU U., et al.

58th ESPE 2019 Meeting, Vienna, Austria, 19 - 21 September 2019, vol.91, no.1, pp.1-682, (Summary Text)

142. Genetic Evaluation of Idiopathic Short Stature

KARAMAN B., BAŞ F., Najaflı A., Avcı Ş., Kardelen A. D., Toksoy G., et al.

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, 6 - 08 September 2019, (Summary Text)

143. The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation

Öztürk A. P., Altunoğlu U., Toksoy G., Karakılıç Özturan E., Poyrazoğlu Ş., Baş F., et al.

58th Annual Meeting of European Society for Paediatric Endocrinology (ESPE), Vienna, Austria, 19 - 21 September 2019, vol.1, no.1, pp.452, (Summary Text)

144. Follow-up of Individuals with Gender Identity Disorders: A Long and Challenging Process

Karakılıç Özturan E., Öztürk A. P., Kardelen Al A. D., Poyrazoğlu Ş., Baş F., Ayaz A. B., et al.

58th Annual ESPE meeting, Vienna, Austria, 19 - 21 September 2019, vol.92, pp.486-487, (Summary Text)

145. Çocuk Endokrinoloji Ünitesinde Yapılan Dinamik Testler ve Yan Etkileri

Yılmaz S., SEMİN N., Karaca N., POYRAZOĞLU Ş., BAŞ F., DARENDELİLER F. F.

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 17 - 21 April 2019, (Summary Text)

146. Konjenital Hipotiroidi Tanılı Ailevi Vakalarda Genetik Etiyolojinin Araştırılması

KARDELEN AL A. D., IŞIK F. B., KARAKILIÇ ÖZTURAN E., SÖZÜGÜZEL M. D., ÖZTÜRK A. P., POYRAZOĞLU Ş., et al.

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 17 - 21 April 2019, (Summary Text)

147. Boy Kısalığının Genetik Etiyolojisinin Araştırılması

KARAMAN B., BAŞ F., NAJAFLI A., AVCI Ş., KARDELEN AL A. D., TOKSOY G., et al.

XXIII Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 17 - 21 April 2019, (Summary Text)

148. 46,XY Cinsiyet Gelişim Bozukluğu Hastalarının Genetik Etyolojisinin Değerlendirilmesi

POYRAZOĞLU Ş., AGHAYEV A., TOKSOY G., KARAMAN B., AVCI Ş., ALTUNOĞLU U., et al.

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 17 April 2019, (Summary Text)

149. Lise öğrencilerinin okul türlerine göre anksiyete ve depresyon açısından karşılaştırılması

Yetim Şahin A., Köse N., Apaydın R., Kılıç A., Baş F.

41. Pediatri Günleri, İstanbul, Turkey, 8 - 10 April 2019, pp.2-3, (Summary Text)

150. Kronik böbrek yetmezlikli ergen ve genç erişkinlerde riskli davranışların ruhsal durum ile ilişkisi.

Güdek K., Yetim Şahin A., Apaydın R., Yılmaz A., Baş F.

Ergen Sağlığı Kongresi, Ankara, Turkey, 22 - 24 March 2019, pp.1-2, (Summary Text)

151. Otoimmün Diyabetin Nadir Bir Nedeni:LRBA Eksikliği

Kardelen Al A. D., Karakılıç Özturan E., Kara M., Güller D., Ceylaner S., Cantez S., et al.

ÇOCUK ENDOKRINOLOJISI OLGU SUNUMLARI -9-, İstanbul, Turkey, 19 - 20 October 2018, pp.14, (Summary Text) Sustainable Development

152. Hiperinsülinemik Hipoglisemiden Diyabete

Karakılıç Özturan E., Kardelen Al A. D., Poyrazoğlu Ş., Baş F., Darendeliler F. F.

ÇOCUK ENDOKRINOLOJISI OLGU SUNUMLARI -9-, İstanbul, Turkey, 19 - 20 October 2018, pp.81, (Summary Text) Sustainable Development

153. Long term side effects of childhood acute lymphoblastic leukemia therapy on bone mineral metabolism

Caliskan S. G., Karaman S., Bas F., Unuvar A., Aydogdu S., Karagenc A. O., et al.

9th International Eurasian Hematology Oncology Congress (EHOC), İstanbul, Turkey, 17 - 20 October 2018, vol.73, (Summary Text)

154. Nationwide Hypophosphatemic Rickets Study

ŞIKLAR Z., TURAN S., BEREKET A., ABACI A., BAŞ F., DEMİR K., et al.

57.th Annual Meeting of the European Society for Paediatric Endocrinology(ESPE), ATİNA, Greece, 27 - 29 September 2018, (Summary Text)

155. Clinical, laboratory and molecular genetic findings of patients with 17beta hydroxysteroid dehydrogenase 3 deficiency

POYRAZOĞLU Ş., TOKSOY G., AGHAYEV A., KARAMAN B., ŞAHİN A., ALTUNOĞLU U., et al.

meeting of European Society of pediatric endocrinology 2018, 27 - 29 September 2018, (Full Text)

156. PROKR2 Mutations in Patients with Growth Hormone Deficiency andMultiple Pituitary Hormone Deficiency

Najaflı A., BAŞ F., KARAMAN B., UYGUNER Z. O., BAŞARAN S., POYRAZOĞLU Ş., et al.

57. ESPE 2018, 27 - 29 September 2018, (Full Text)

157. Evaluation of Three Patients with 46,XY Gonadal Dysgenesis due to Desert Hedgehog Gene Mutations

POYRAZOĞLU Ş., KARAMAN B., BAŞ F., Darendeliler F., TOKSOY G., BAŞARAN S., et al.

57th Annual Meeting of the European Society for Paediatric Endocrinology, Atina, Greece, 27 - 29 September 2018, pp.558, (Full Text)

158. Evaluation of Genetic Etiology in Patients with 46,XY Disorders of Sex Development: One Center Experience

AGHAYEV A., TOKSOY G., POYRAZOĞLU Ş., KARAMAN B., AVCI Ş., YILDIZ M., et al.

57th ESPE 2018 Meeting, Atina, Greece, 27 September 2018, (Summary Text)

159. Copy-Number Variations of the Human Olfactory Receptor Gene Family in Patients with Macromastia and Prepubertal Gynecomastia

BAŞ F., KARAMAN B., KARDELEN AL A. D., HEIDARGHOLİZADEH S., NAJAFLI A., TOKSOY G., et al.

57th ESPE 2018 Meeting, Atina, Greece, 27 September 2018, (Summary Text)

160. Copy-Number Variations of the Human Olfactory Receptor Gene Familyin Patients with Macromastia and Prepubertal Gynecomastia

BAŞ F., KARAMAN B., UYGUNER Z. O., BAŞARAN S., POYRAZOĞLU Ş., DARENDELİLER F. F., et al.

57. ESPE 2018, 27 - 29 September 2018, (Full Text)

161. Evaluation of Genetic Etiology in Patientswith 46,XY Disorders of SexDevelopment:One Center Experience

aghayev a., BAŞ F., KARAMAN B., UYGUNER Z. O., BAŞARAN S., POYRAZOĞLU Ş., et al.

57. ESPE 2018, 27 - 29 September 2018, (Full Text)

162. Vascularity Index via Superb Microvascular Imaging is PositivelyCorrelated With Radioactive Iodine Uptake andDosage of Medication in Thyroid Dyshormonogenesis

BAYRAMOĞLU Z., ÇALIŞKAN E., YILMAZ R. S., AKYOL SARI Z. N., KARDELEN A. D., POYRAZOĞLU Ş., et al.

Euroson 2018, 6 - 09 September 2018, (Full Text)

163. Osteoporosis-pseudoglioma Syndrome (OPPG): Improvement of Osteoporosis on Biphosphonate Therapy

Karakılıç Özturan E., Altunoğlu U., Kardelen Al A. D., Yavaş Abalı Z., Avcı Ş., Kayserili Karabay H., et al.

57th Annual ESPE, Athens, Greece, 27 - 29 September 2018, vol.89, pp.90, (Summary Text)

164. 21 HİDROKSİLAZ EKSİKLİĞİNE BAĞLI KLASİK OLMAYAN KONJENİTAL ADRENAL HİPERPLAZİDE KLİNİK, LABORATUVAR, GENETİK ÖZELLİKLER, TEDAVİYE ALINAN YANITLAR VE ULAŞILAN FİNAL BOY VERİLERİ

SAVAŞ ERDEVE Ş., ÇETİNKAYA S., YAVAŞ ABALI Z., POYRAZOĞLU Ş., BAŞ F., BERBEROĞLU M., et al.

22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET DERNEĞİ, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)

165. Endokrin Hastalıklarda Çocukluktan Erişkine Geçiş

Karakılıç Özturan E., Kardelen A. D., Kubat Üzüm A., Özçetin M., Baş F., Poyrazoğlu Ş., et al.

XXII. Ulusal Pediatrik Endokronoloji ve Diyabet Kongresi , Antalya, Turkey, 18 - 22 April 2018, pp.118, (Summary Text)

166. Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

ŞIKLAR Z., TURAN S., BEREKET A., ABACI A., GÜRAN T., DEMİR K., et al.

22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)

167. Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: 38.936 Bebeği Kapsayan Pilot Çalışma Verilerinin Değerlendirilmesi

GÜRAN T., tezel b., GÜRBÜZ F., SELVER EKLİOĞLU B., HATİPOĞLU N., KARA C., et al.

XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)

168. Çocuklarda hipogonadizm tedavisine yaklaşım

BAŞ F.

22. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 17 - 22 April 2018, (Full Text)

169. Clinical findings and genetic analysis of patients with macromastia and prepubertal gynecomastia

DARENDELİLER F. F., BAŞ F., KARAMAN B., POYRAZOĞLU Ş., KARDELEN A. D., TOKSOY G., et al.

ENDO 2018, 23 - 26 March 2018, (Full Text)

170. Molecular Genetic diagnostıc efficiency of targeted next generation sequencing on “disorders of sex development”.

TOKSOY G., AGHAYEV A., POYRAZOĞLU Ş., AVCI Ş., KARAMAN B., YAVAŞ ABALI Z., et al.

ERCIYES MEDİCAL GENETICS DAYS, Turkey, 7 - 10 March 2018, no.1, (Full Text)

171. Characteristics in 5-Alpha Reductase Type 2 Deficiency: A Multicenter Study from Turkey.

ABACI A., ÇATLI G., Kırbıyık Ö., ŞAHİN N. M., ABALI Z. Y., ÜNAL E., et al.

10th International Meeting of Pediatric Endocrinology, 10 - 17 September 2017, (Summary Text)

172. A rare cause of congenital adrenal hyperplasia: Clinical and genetic findings and follow-up of six patients with 17 hydroxylase deficiency.

KARDELEN A. D., BAŞ F., TOKSOY G., POYRAZOĞLU Ş., BUNDAK R., ALTUNOĞLU U., et al.

10 th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2017, vol.88, pp.457-458, (Summary Text)

173. The relation between urinary Bisphenol A levels and body weight among children.

Kılıç A., Gümüş S., Yetim Şahin A., Özçetin M., Baş F., Darendeliler F.

American Academy of Pediatrics Experience National Conference and Exhibition, Michigan, United States Of America, 16 - 19 September 2017, pp.10-11, (Full Text)

174. PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY.

ABACI A., ÇATLI G., kırbıyık ö., şahin n., YAVAŞ ABALI Z., ünal e., et al.

IMPE 2017, 14 - 17 September 2017, (Summary Text)

175. The relationship of obesity and insulin resistance with hyperandrogenemia, anti-Müllerian hormone, inhibin A, inhibin B and insulin-like peptide-3 levels in patients with polycystic ovary syndrome

YETİM A., BAŞ F., YETİM Ç., POYRAZOĞLU Ş., BUNDAK R., DARENDELİLER F. F.

10 th International Meeting of Pediatric Endocrinology, 14 - 17 September 2017, (Summary Text)

176. Uncovering a new mechanism in the pigmentary hypertrichosis and non-autoimmune diabetes mellitus (PHID) syndrome involving the 3’ UTR

Riachi M., DARENDELİLER F. F., BAŞ F., Hussain K.

10 th International Meeting of Pediatric Endocrinology Meeting, Washington, Kiribati, 14 - 17 September 2017, (Summary Text)

177. The assessment of growth hormone treatment and adult height in patients with growth hormone deficiency

POYRAZOĞLU Ş., VAZGEÇER OGULTEKIN E., BAŞ F., BUNDAK R., DARENDELİLER F. F.

10 th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2017, (Summary Text)

178. Increased aortic diameters in normotensive children and adolescents with Turner syndrome with emphasis on associations with B-type natriuretic peptide and insülin like growth factors

UÇAR A., AKSAKAL M. Z., OĞUZ E., YEKELER E., BAŞ F., POYRAZOĞLU Ş., et al.

10 th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2017, (Summary Text)

179. 45,X/46,XY MOSAICISM: CLINICAL CHARACTERISTICS AND FOLLOW-UP DATA45,X/46,XY MOSAICISM: CLINICAL CHARACTERISTICS AND FOLLOW-UP DATA

POYRAZOĞLU Ş., BAŞ F., BUNDAK R., DARENDELİLER F. F.

6th international DSD symposium, 29 June - 01 July 2017, (Summary Text)

180. Ondört Yıldır İzlenen Wolcott Rallison Sendromu (WRS) Tanılı Bir Olgu

ÇAM S., ARSLANOĞLU İ., BOLU S., BAŞ F., BUNDAK R.

XXI. Ulusal Pediatrik Endokrinoloji Kongresi, Turkey, 26 - 30 April 2017

181. 5-Alfa Redüktaz Tip 2 Eksikliği Tanılı Olguların Fenotipik, Hormonal ve Moleküler Genetik Özellikleri: Çok Merkezli Ulusal Veriler

ABACI A., ÇATLI G., KIRBIYIK Ö., MURATOĞLU ŞAHİN N., YAVAŞ ABALI Z., UNAL E., et al.

XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 26 April 2017, (Summary Text)

182. Ondört yıldır izlenen Wolcott Rallison Sendromu (WRS) tanılı olgu

ÇAM S., ARSLANOĞLU İ., BOLU S., BAŞ F., BUNDAK R.

XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 26 - 30 April 2017, (Summary Text)

183. Nadir görülen konjenital adrenal hiperplazi nedeni: 17-hidroksilaz eksikliği tanılı vakalarımızın klinik ve genetik bulguları, izlem özellikleri

KARDELEN A. D., BAŞ F., TOKSOY G., POYRAZOĞLU Ş., BUNDAK R., ALTUNOĞLU U., et al.

XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 26 - 30 April 2017, (Summary Text)

184. Çocuklarda Vücut Kompozisyon Analizi ve Vitamin D Düzeyi

Khalilova F., Kılıç A., Yetim Şahin A., Baş F., Özçetin M., Eliuz Tipici B., et al.

39. Pediatri Günleri, İstanbul, Turkey, 3 - 05 April 2017, pp.43-44, (Summary Text)

185. Yenidoğanda biyotine bağlı biyokimyasl hipertiroidi.

Ulak Özkan M., KARDELEN AL A. D., GÜNEŞ D., POYRAZOĞLU Ş., BAŞ F., Bundak R., et al.

39.Pediatri Günleri ve 18. Pediatri Hemşireliği Günleri, İstanbul, Turkey, 2 - 05 April 2017, pp.170, (Summary Text)

186. Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 (PIT1) gene mutation

YAVAŞ ABALI Z., BAŞ F., POYRAZOĞLU Ş., BUNDAK R., DARENDELİLER F. F.

The Endocrine Society’s 99 th Annual Meeting, 1 - 04 April 2017, (Summary Text)

187. 46, XY Cinsiyet Gelişim Bozukluğu olan Dört Olguda AR ve SRD5A2 Geninde Yeni Mutasyonlar

Aghayev A. R., Toksoy G., Baş F., Altunoğlu U., Karaman B., Poyrazoğlu Ş., et al.

2. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 23 - 25 February 2017, pp.1, (Full Text)

188. Erken ergenlik olgular ile Uzmanına danışalım

BAŞ F.

60. Türkiye Milli Pediatri Kongresi, Antalya, Turkey, 9 - 13 November 2016

189. Sınırda Erken Puberteli ve Normal Fizyolojik Puberteli Kız Çocuklarında Kemik Yaşı ve Öngörülen Erişkin Boy Temelinde Gonadotropin Salgılatıcı Hormon Analoglarının (GnRHa) Final Boya Etkisi

Hızlı Demirkale Z., Baş F., Poyrazoğlu Ş., Darendeliler F. F.

XX. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Turkey, 5 - 09 October 2016, pp.201, (Summary Text)

190. Türkiyenin kuzey batı bölgesinde çocukluk döneminde tip 1 diyabet insidansı

POYRAZOĞLU Ş., BUNDAK R., YAVAŞ ABALI Z., İŞSEVER H., BAŞ F., DARENDELİLER F. F.

XX. Ulusal Pediatrik Endokrinoloji ve Diyabet kongresi, İzmir, Turkey, 6 - 09 October 2016

191. Türkiye nin Kuzey Batı Bölgesinde Çocukluk Döneminde Tip 1 Diyabet İnsidansı

POYRAZOĞLU Ş., BUNDAK R., Yavaş Abalı Z., İşsever H., BAŞ F., DARENDELİLER F. F., et al.

XX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 5 - 09 October 2016

192. 21 hidroksilaz eksikliğine bağlı klasik olmayan konjenital adrenal hiperplazide klinik laboratuvar genetik özellikler tedaviye alınan yanıtlar ve ulaşılan final boy verileri Ulusal örneklem

ERDEVE SAVAŞ Ş., ÇETİNKAYA S., YAVAŞ ABALI Z., POYRAZOĞLU Ş., BAŞ F., BERBEROĞLU M., et al.

XX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 5 - 08 October 2016

193. Hipotalamo hipofizer hastalıkların perioperatif yönetimi

BAŞ F.

XX. Ulusal Pediatrik Endokrin ve Diyabet Kongresi, Antalya, Turkey, 5 - 08 October 2016, (Full Text)

194. Polikistik over sendromlu olgularda insülin direnci ile hiperandrojenemi inhibin A inhibin B ve insülin like peptid 3 düzeyleri ile ilişkisinin araştırılması

YETİM A., BAŞ F., KILIÇ A., DARENDELİLER F. F.

XX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 5 - 08 October 2016, (Full Text)

195. Onset of puberty in healthy boys is associated with a decreased BMI compared to values prior to the onset of puberty

BUNDAK R., DARENDELİLER F. F., BAŞ F., POYRAZOĞLU Ş., GÜNÖZ H., NEYZİ O.

55 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Paris, France, 10 - 12 September 2016, vol.86, pp.290, (Summary Text)

196. Clinical characteristics and molecular analysis of patients with neonatal diabetes

YAVAŞ ABALI Z., BUNDAK R., BAŞ F., De FRANCO E., GENENŞ M., POYRAZOĞLU Ş., et al.

55 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Paris, France, 10 - 12 September 2016, vol.86, pp.211, (Summary Text)

197. Effect of gonadotropin releasing hormone analogues GnRHa on final height in girls with borderline early puberty or normal physiological puberty depend on bone age advancement and predicted height

HIZLI Z., BAŞ F., POYRAZOĞLU Ş., GENENŞ M., YAVAŞ ABALI Z., BUNDAK R., et al.

55 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Paris, France, 10 - 12 September 2016, vol.86, pp.436, (Summary Text)

198. Clinicopathological characteristics of papillary thyroid cancer in children with emphasis on the pubertal status and association with BRAF V600E mutation

POYRAZOĞLU Ş., BUNDAK R., BAŞ F., DARENDELİLER F. F.

55 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Paris, France, 10 - 12 September 2016, vol.86, pp.481, (Summary Text)

199. Precocious puberty in patients with primary adrenal insufficiency due to melanocortin receptor 2 mutation

BAŞ F., YAVAŞ ABALI Z., GÜRAN T., GENENŞ M., POYRAZOĞLU Ş., POYRAZOĞLU Ş., et al.

55 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE, Paris, France, 10 - 12 September 2016, vol.86, pp.418, (Summary Text)

200. The 3M syndrome A cause of pre and post natal severe growth retardation

GENENŞ M., ALTUNOĞLU U., BAŞ F., POYRAZOĞLU Ş., YAVAŞ ABALI Z., BUNDAK R., et al.

55 th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Paris, France, 10 - 12 September 2016, vol.86, pp.465, (Summary Text)

201. Ağır büyüme geriliği olan diyabetli olguda SLC29A3 gen mutasyonu

YAVAŞ ABALI Z., BAŞ F., KESKİN M., GENENŞ M., POYRAZOĞLU Ş., BUNDAK R., et al.

Çocuk Endokrinolojisi Olgu Sunumları-8, Adana, Turkey, 29 April - 30 June 2016

202. Silver Russel sendromunda erken puberte Tanı sürecinde klinik ve laboratuvar bulguları arasındaki uyumsuzluk

POYRAZOĞLU Ş., YAVAŞ ABALI Z., BAŞ F., GENENŞ M., BUNDAK R., DARENDELİLER F. F.

Çocuk Endokrinolojisi Olgu Sunumları-8, Turkey, 29 - 30 April 2016

203. Tiroid Fonksiyon Testleri ile Tiroid Hastalıkları Olgular Eşliğinde Değerlendirme

BAŞ F., YAVAŞ ABALI Z., GENENŞ M.

MEZUNİYET SONRASI EĞİTİM, İstanbul, Turkey, 06 April 2016