Prof. ŞÜKRAN POYRAZOĞLU

Publication Network

Articles 226

1. Gonadal Function and Its Evolution in 46,XX Testicular/Ovotesticular DSD

Sepich M., Bertelloni S., Tyutyusheva N., Lucas-Herald A., Mazen I., Cools M., et al.

Journal of Clinical Endocrinology and Metabolism , vol.111, no.5, 2026 (SCI-Expanded, Scopus)

2. Identifying Genetic Factors Contributing to Non-Syndromic Early-Onset Childhood Obesity Utilizing Whole-Exome Sequencing in Consanguineous Families

Olgun H. B., Poyrazoğlu Ş., Tuncer Kılınç F. N.

Genes , vol.17, pp.1-16, 2026 (Peer-Reviewed Journal)

3. Glucocorticoid-prescribing trends in congenital adrenal hyperplasia, 2017 to 2023

Roxas A., Gihawi A., Makarchuk M., Bryce J., Chen M., Ahmed S. F., et al.

ENDOCRINE CONNECTIONS , vol.15, no.3, 2026 (SCI-Expanded, Scopus)

4. 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)

5. Evaluation of rare NR1D2 variants in MODY-X: clinical, genetic, and in silico insights.

Aydogan C., Kanca-Demirci D., Gul N., Poyrazoglu Ş., Tokat B., Mutlu U., et al.

Journal of endocrinological investigation , 2026 (SCI-Expanded, Scopus)

6. 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)

7. 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

8. 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)

9. 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)

10. Gender differences in the distribution of IDL, LDL, and HDL lipoprotein subfractions in MODY compared to type 2 diabetes: Data from the MODY-Ist study

YILMAZ AYDOĞAN H., Demirci D. K., GÜL N., YANAR F., POYRAZOĞLU Ş., Yilmaz S. G., et al.

JOURNAL OF DIABETES AND ITS COMPLICATIONS , vol.39, no.12, 2025 (SCI-Expanded, Scopus) Sustainable Development

11. 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)

12. Phenotypic Variation and Pubertal Outcomes in Males and Females With 46,XY Partial Gonadal Dysgenesis

Tadokoro-Cuccaro R., Hughes I. A., Cools M., van de Vijver K., de Mendonca B. B., Domenice S., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.110, no.12, 2025 (SCI-Expanded, Scopus) Sustainable Development

13. 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)

14. **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

15. 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

16. Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study

Ozgen I. T., KANDEMİR T., YILDIZ M., POYRAZOĞLU Ş., ŞIKLAR Z., Abseyi N. S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.38, no.8, pp.830-837, 2025 (SCI-Expanded, Scopus) Sustainable Development

17. 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)

18. Blood pressure and its associations in 554 children and young people with congenital adrenal hyperplasia

Lawrence N. R., Bacila I., Tonge J., Dawson J., Collins G. S., Lang Z., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.192, no.5, pp.529-539, 2025 (SCI-Expanded, Scopus)

19. 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

20. Prevalence and management of hypertension in Turner syndrome: data from the International Turner Syndrome (I-TS) registry

Mathara Diddhenipothage S. A. D., Beck K. J., Amiyangoda G., Bryce J., Cima L., De Groote K., et al.

ENDOCRINE CONNECTIONS , vol.14, no.2, 2025 (SCI-Expanded, Scopus) Sustainable Development

21. 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)

22. 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)

23. 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)

24. **Target gene variations of PPAR isoforms may contribute to MODY heterogeneity: A preliminary comparative study with type 2 diabetes**

Yilmaz-Aydogan H., Kanca-Demirci D., Gul N., Aydogan C., Poyrazoglu Ş., Tutuncu Y., et al.

DIABETES RESEARCH AND CLINICAL PRACTICE , vol.218, 2024 (SCI-Expanded, Scopus)

25. Investigating Leptin Gene Variants and Methylation Status in Relation to Breastfeeding and Preventing Obesity

Kilic A., Pehlivan S., Varkal M. A., Tuncel F. C., Kandemir I., Ozcetin M., et al.

CHILDREN-BASEL , vol.11, no.11, 2024 (SCI-Expanded, Scopus) Sustainable Development

26. 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)

27. 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)

28. Temporal Trends in Acute Adrenal Insufficiency Events in Children With Congenital Adrenal Hyperplasia During 2019-2022

Tseretopoulou X., Ali S. R., Bryce J., Amin N., Atapattu N., Bachega T. A. S. S., et al.

JOURNAL OF THE ENDOCRINE SOCIETY , vol.8, no.10, 2024 (ESCI, Scopus) Sustainable Development

29. Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

Şıklar Z., Özsu E., Kızılcan Çetin S., Özen S., Çizmecioğlu-Jones F., Balkı H. G., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.16, no.3, pp.288-296, 2024 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

30. 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)

31. Characterization of 35 Novel NR5A1/SF-1 Variants Identified in Individuals With Atypical Sexual Development: The SF1next Study

Naamneh Elzenaty R., Martinez de Lapiscina I., Kouri C., Sauter K., Sommer G., Castaño L., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , 2024 (SCI-Expanded, Scopus) Sustainable Development

32. 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

33. Whole Exome Sequencing Revealed Paternal Inheritance of Obesity-related Genetic Variants in a Family with an Exclusively Breastfed Infant

Olgun Celebioglu H. B., Ozturk A. P., Poyrazoglu Ş., Tuncer F. N.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.16, no.4, pp.450-457, 2024 (SCI-Expanded, Scopus, TRDizin)

34. Metabolic Syndrome and Type 2 Diabetes Mellitus in Overweight and Obese Children: A Single Centre Experience

Demirbuga A., Poyrazoglu Ş., Bundak R.

JOURNAL OF CHILD - COCUK DERGISI , no.3, pp.154-161, 2024 (ESCI, TRDizin)

35. Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

Kouri C., Sommer G., Martinez de Lapiscina I., Elzenaty R. N., Tack L. J. W., Cools M., et al.

EBIOMEDICINE , vol.99, 2024 (SCI-Expanded, Scopus) Sustainable Development

36. Long-term 10-year comparison of girls with congenital adrenal hyperplasia who underwent early and late feminizing genitoplasty

Erginel B., Ozdemir B., Karadeniz M., Poyrazoglu Ş., Keskin E., Soysal F. G.

PEDIATRIC SURGERY INTERNATIONAL , vol.39, no.1, 2023 (SCI-Expanded, Scopus) Sustainable Development

37. 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)

38. Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study

Schröder M. A. M., Neacşu M., Adriaansen B. P. H., Sweep F. C. G. J., Ahmed S. F., Ali S. R., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , vol.189, no.4, pp.460-468, 2023 (SCI-Expanded, Scopus) Sustainable Development

39. Predictors of surgical complications in boys with hypospadias: data from an international registry

Scougall K., Bryce J., Baronio F., Boal R. L., Castera J. R., Castro S., et al.

WORLD JOURNAL OF PEDIATRIC SURGERY , vol.6, no.4, 2023 (ESCI, Scopus) Sustainable Development

40. 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)

41. A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review

Besci Ö., Fırat S. N., Özen S., Çetinkaya S., Akın L., Kör Y., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.108, no.9, pp.2371-2388, 2023 (SCI-Expanded, Scopus) Sustainable Development

42. 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)

43. 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)

44. 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

45. 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)

46. Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls

Guaragna-Filho G., Guerra-Junior G., Tadokoro-Cuccaro R., Hughes I. A., Barros B. A., Hiort O., et al.

SEXUAL DEVELOPMENT , vol.17, no.1, pp.16-25, 2023 (SCI-Expanded, Scopus) Sustainable Development

47. 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

48. 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

49. 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

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. 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)

52. 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)

53. 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)

54. 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)

55. 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

56. 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)

57. 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)

58. 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)

59. Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry.

Lawrence N., Bacila I., Dawson J., Bryce J., Ali S. R., van den Akker E. L. T., et al.

Clinical endocrinology , vol.97, no.5, pp.551-561, 2022 (SCI-Expanded, Scopus)

60. An International Study of the Association between Local Health Care Resources and Acute Adrenal Insufficiency Events in Children with Congenital Adrenal Hyperplasia

Tseretopoulou X., Ali S. R., Bryce J., Navoda A., Birkebaek N. H., Baronio F., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.401-402, 2022 (SCI-Expanded, Scopus)

61. Blood pressure (BP) status in Congenital Adrenal Hyperplasia (CAH) - longitudinal analysis of real world data from the I-CAH registry

Lawrence N. R., Bacila I., Dawson J., Ali S. R., van den Akker E. L. T., Sartori Sanchez Bachega T. A., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.112-113, 2022 (SCI-Expanded, Scopus)

62. Gonadal morphology in 46,XY gonadal dysgenesis: I-DSD Registry-based study

Tadokoro-Cuccaro R., Hughes I., Cools M., van de Vijver K., de Mendonca B. B., Domenice S., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.44-45, 2022 (SCI-Expanded, Scopus)

63. Predictors of surgical outcomes in boys with hypospadias

Scougall K., Bryce J., Baronio F., Boal R. L., Castera R., Castro S., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.376-377, 2022 (SCI-Expanded, Scopus)

64. 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)

65. **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)

66. 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)

67. 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)

68. 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)

69. A National Multicenter Study of Leptin (LEP) and Leptin Receptor (LEPR) Deficiency and a Systematic Review of Patients with Pathogenic LEP/LEPR Variants

BESCİ Ö., Firat S. N., ÖZEN S., Cetinkaya S., Akin L., Kor Y., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.239, 2022 (SCI-Expanded, Scopus)

70. Treatment of congenital adrenal hyperplasia in children aged 0-3 years: A retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure.

Neumann U., van der Linde A., Krone R. E., Krone N. P., Güven A., Güran T., et al.

European journal of endocrinology , vol.187, pp.587-596, 2022 (SCI-Expanded, Scopus)

71. 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)

72. 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

73. 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

74. 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)

75. 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)

76. 46,XY Partial gonadal dysgenesis; diagnosis and long-term outcome at puberty

Cuccaro R. T., Hughes I., Cools M., van de Vijver K., de Mendonca B. B., Domenice S., et al.

SEXUAL DEVELOPMENT , no.SUPPL 1, pp.33-35, 2022 (SCI-Expanded, Scopus)

77. Predictors of surgical outcomes in boys with hypospadias

Scougall K., Bryce J., Baronio F., Boal R. L., Roberto Castera J., Castro S., et al.

SEXUAL DEVELOPMENT , no.SUPPL 1, pp.73-75, 2022 (SCI-Expanded, Scopus)

78. 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

79. Precision Diagnosis of Maturity-Onset Diabetes of the Young with Next-Generation Sequencing: Findings from the MODY-IST Study in Adult Patients

Aydogan H., Gul N., Demirci D. K., Mutlu Ü., Gulfidan G., Arga K. Y., et al.

OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY , vol.26, no.4, pp.218-235, 2022 (SCI-Expanded, Scopus) Sustainable Development

80. 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

81. Growth, puberty and testicular function in boys born small for gestational age with a nonspecific disorder of sex development.

Tack L. J. W., van der Straaten S., Riedl S., Springer A., Holterhus P., Hornig N. C., et al.

Clinical endocrinology , vol.96, no.2, pp.165-174, 2022 (SCI-Expanded, Scopus)

82. 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

83. The Role of American Thyroid Association Pediatric Thyroid Cancer Risk Stratification and BRAF^V600E Mutation in Predicting the Response to Treatment in Papillary Thyroid Cancer Patients ≤18 Years Old

Giles Senyurek Y., Iscan Y., Sormaz İ. C., Poyrazoglu Ş., Tunca F.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.14, no.2, pp.196-206, 2022 (SCI-Expanded, Scopus, TRDizin)

84. 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)

85. 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)

86. 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)

87. 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

88. 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)

89. 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)

90. **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)

91. Broad range of phenotypes in an international cohort of 75 DSD individuals with SF-1/NR5A1 variants

Kouri C., Sommer G., Ahmed F., Balsamo A., Baronio F., Bryce J., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.87-89, 2021 (SCI-Expanded, Scopus)

92. Variation of glucocorticoid dose and biomarkers in children with congenital adrenal hyperplasia longitudinal analysis of real world data from the I-CAH registry

Lawrence N., Bacila I., Dawson J., Bryce J., van den Akker E. L., Sartori Sanchez Bachega T. A., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.26, 2021 (SCI-Expanded, Scopus)

93. 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)

94. 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)

95. 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)

96. Long-Term Cardiometabolic Morbidity in Young Adults with Classic 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia

Righi B., Ali S. R., Bryce J., Tomlinson J. W., Bonfig W., Baronio F., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.69-70, 2021 (SCI-Expanded, Scopus)

97. 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)

98. International practice of therapy monitoring in congenital adrenal hyperplasia - Real World data from the I-CAH registry

Lawrence N., Bacila I., Dawson J., Bryce J., van den Akker E., Sartori Sanchez Bachega T. A., et al.

HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 1, pp.67-68, 2021 (SCI-Expanded, Scopus)

99. 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)

100. Monogenic Childhood Diabetes: Dissecting Clinical Heterogeneity by Next-Generation Sequencing in Maturity-Onset Diabetes of the Young

Kanca Demirci D., Darendeliler F. F., Poyrazoglu Ş., Al A. D., Gül N., Tutuncu Y., et al.

OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY , vol.25, no.7, pp.431-449, 2021 (SCI-Expanded, Scopus)

101. 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)

102. 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)

103. 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

104. Gonadectomy in conditions affecting sex development: a registry-based cohort study.

Lucas-Herald A. K., Bryce J., Kyriakou A., Ljubicic M. L., Arlt W., Audi L., et al.

European journal of endocrinology , vol.184, no.6, pp.791-801, 2021 (SCI-Expanded, Scopus)

105. International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia: data from the I-CAH registry.

Bacila I., Freeman N., Daniel E., Sandrk M., Bryce J., Ali S. R., et al.

European journal of endocrinology , vol.184, pp.553-563, 2021 (SCI-Expanded, Scopus)

106. 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

107. 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)

108. Testosterone Therapy and Its Monitoring in Adolescent Boys with Hypogonadism: Results of an International Survey from the I-DSD Registry.

Stancampiano M. R., Lucas-Herald A. K., Bryce J., Russo G., Barera G., Balsamo A., et al.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation , vol.15, no.4, pp.236-243, 2021 (SCI-Expanded, Scopus) Sustainable Development

109. 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

110. Real World Estimates Of Adrenal Insufficiency Related Adverse Events In Children With Congenital Adrenal Hyperplasia.

Ali S., Bryce J., Haghpanahan H., Lewsey J., Tan L., Atapattu N., et al.

The Journal of clinical endocrinology and metabolism , vol.106, 2021 (SCI-Expanded, Scopus)

111. Surgical Practice in Girls with Congenital Adrenal Hyperplasia: An International Registry Study.

Hebenstreit D., Ahmed F. S., Krone N., Krall C., Bryce J., Alvi S., et al.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation , vol.15, no.4, pp.229-235, 2021 (SCI-Expanded, Scopus)

112. **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

113. 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)

114. 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)

115. 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)

116. Conservative Management of Vaginal Hypoplasia

DURAL Ö., POYRAZOĞLU Ş.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.12, pp.50-52, 2020 (SCI-Expanded, Scopus, TRDizin)

117. Hormone Replacement Therapy in a Patient with Hypogonadism and Coexisting Medical Conditions

DURAL Ö., POYRAZOĞLU Ş.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.12, pp.46-49, 2020 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

118. 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

119. 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)

120. 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)

121. 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)

122. 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)

123. 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)

124. 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)

125. 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)

126. 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)

127. Long-Term Outcome In Leydig Cell Hypoplasia

Boncompagni A., Bryce J., Lucaccioni L., Iughetti L., Acerini C., Cuccaro R. T., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.259, 2019 (SCI-Expanded, Scopus)

128. 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)

129. 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)

130. 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)

131. 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)

132. 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)

133. 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)

134. 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)

135. 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)

136. Joubert syndrome with multiple pituitary hormone deficiency.

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

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

137. Oral Bacteria of Children with Turner Syndrome

Unsal G., Topcuoglu N., Guven Y., Poyrazoglu S., Kulekci G., Aktoren O.

JOURNAL OF PEDIATRIC RESEARCH , vol.6, no.1, pp.44-50, 2019 (ESCI, TRDizin)

138. 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)

139. 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)

140. 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)

141. 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

142. 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

143. 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)

144. 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)

145. 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)

146. 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)

147. 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)

148. 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)

149. 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)

150. 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)

151. 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)

152. 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)

153. 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)

154. 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)

155. Gonadectomy for Adults With DSD Conditions In The International Disorders of Sex Development Registry

Lucas-Herald A. K., Kyriakou A., Bryce J., Rodie M., Acerini C., Arlt W., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.549-550, 2018 (SCI-Expanded, Scopus)

156. 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)

157. 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)

158. 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)

159. 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)

160. 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)

161. 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

162. 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)

163. 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)

164. Potential risk factors for vitamin D levels in medium- and long-term use of antiepileptic drugs in childhood.

YILDIZ E., POYRAZOGLU Ş., Bektas G., KARDELEN A. D., AYDıNLı N.

Acta neurologica Belgica , vol.117, pp.447-453, 2017 (SCI-Expanded, Scopus)

165. 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)

166. Birth Weight in Different Etiologies of Disorders of Sex Development.

Poyrazoglu S., DARENDELILER F. F., AHMED S., HUGHES I., BRYCE J., JIANG J., et al.

The Journal of clinical endocrinology and metabolism , vol.102, pp.1044-1050, 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. 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)

169. 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

170. 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)

171. 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)

172. 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)

173. Classic Architecture with Multicentricity and Local Recurrence, and Absence of TERT Promoter Mutations are Correlates of BRAF(V600E) Harboring Pediatric Papillary Thyroid Carcinomas

Onder S., Sari S. O., Yegen G., Sormaz I. C., Yilmaz I., Poyrazoglu S., et al.

ENDOCRINE PATHOLOGY , vol.27, no.2, pp.153-161, 2016 (SCI-Expanded, Scopus)

174. 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)

175. 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)

176. 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)

177. 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)

178. 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

179. 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

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. 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)

182. Obezite ve Vitamin-Mineral İlişkisi

Poyrazoğlu Ş.

Türkiye Klinikleri Pediatri Dergisi , vol.11, no.3, pp.36-41, 2015 (Peer-Reviewed Journal) Sustainable Development

183. 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)

184. 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)

185. 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)

186. 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)

187. 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)

188. Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

Poyrazoglu S., Akcay T., Arslanoglu I., Atabek M. E., Atay Z., Berberoglu M., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.1, pp.37-44, 2015 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

189. Dentofacial Findings in Turner Syndrome

Şahin Ünsal G., Poyrazoğlu Ş., Saka H. N., Ulukapı I.,

Ege Üniversitesi Diş Hekimliği Fakültesi , vol.36, no.1, pp.10-18, 2015 (TRDizin)

190. Turner Sendromlu Çocukların Ağız İçi Bulguları

Ünsal G. Ş., Poyrazoğlu Ş., Saka H. N., Ulukapı I.,

Türkiye Klinikleri Pediatri Dergisi , vol.1, no.1, pp.1-6, 2015 (TRDizin)

191. 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

192. 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)

193. 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)

194. 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

195. 2013 Lwpes/Espe 9th Joint Meeting, Milan, Italy, Selected Highlights

Poyrazoglu S., Volkl T. M. K., Karantza M.

PEDIATRIC ENDOCRINOLOGY REVIEWS PER , vol.11, no.3, pp.328-336, 2014 (SCI-Expanded, Scopus)

196. 2013 lwpes/espe gth joint Meeting, Milan, Italy, selected highlights

POYRAZOĞLU Ş., Volkl T. M., Karantza M.

Pediatric Endocrinology Reviews , vol.11, no.3, pp.328-336, 2014 (Scopus)

197. 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

198. 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)

199. 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

200. Aralık Sayısının “Tanınız Nedir?” Yanıtı: Hipertiroidi Basedow Graves Hastalığı

Kılıç A., Poyrazoğlu Ş., Soydemir D., Yıldız İ.

Çocuk Dergisi , vol.13, no.1, pp.51-54, 2013 (TRDizin)

201. 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)

202. 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)

203. 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)

204. 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

205. Prevalence of Testicular Microlithiasis in Males with Congenital Adrenal Hyperplasia and Its Association with Testicular Adrenal Rest Tumors

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

HORMONE RESEARCH IN PAEDIATRICS , vol.73, no.6, pp.443-448, 2010 (SCI-Expanded, Scopus)

206. 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)

207. 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)

208. Glucocorticoid receptor gene polymorphisms and their relation with glucocorticoid sensitivity and obesity in patients with congenital adrenal hyperplasia

Saka N., Poyrazoglu S., Sayitoglu M., Ozbek U., Sen N., ISGUVEN P., et al.

HORMONE RESEARCH , vol.72, pp.346, 2009 (SCI-Expanded) Sustainable Development

209. 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)

210. Severe short stature: an unusual finding in lipoid proteinosis.

POYRAZOĞLU Ş., Günöz H., Darendeliler F.

Journal of clinical research in pediatric endocrinology , vol.1, no.2, pp.97-101, 2008 (Scopus)

211. 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)

212. 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

213. 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)

214. 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)

215. Evaluation of permanent growth hormone deficiency (GHD) in young adults with childhood onset GHD: A multicenter study

BERBEROĞLU M., ŞIKLAR Z., Darendeliler F. F., Poyrazoglu S., DARCAN Ş., Isguven P., et al.

HORMONE RESEARCH , vol.70, pp.103, 2008 (SCI-Expanded)

216. 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)

217. 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)

218. 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)

219. Ergenlik Gecikmesi

BAŞ F., POYRAZOĞLU Ş., DARENDELİLER F. F.

Türkiye Klinikleri Pediatrik Bilimler , vol.2, no.10, pp.24-31, 2006 (Peer-Reviewed Journal)

220. 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)

221. 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)

222. 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

223. Haemophilus influenzae type b carriage among 3- to 24-month-old Turkish children

POYRAZOGLU S., KOMEC S., Gokcay G. F., Ongen B.

EPIDEMIOLOGY AND INFECTION , vol.133, no.6, pp.1113-1117, 2005 (SCI-Expanded, Scopus)

224. 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)

225. 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

226. Serum leptin levels in patients with 21-hydroxylase deficiency before and after treatment

POYRAZOGLU S., GUNOZ H., Darendeliler F. F.

TURKISH JOURNAL OF PEDIATRICS , vol.45, no.1, pp.33-38, 2003 (SCI-Expanded, Scopus)

Papers Presented at Peer-Reviewed Scientific Conferences 173

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. Friedreich ataxia and impaired steroidogenesis

Bayrak Demirel Ö., Öney C., Akbaş S., Kandemir T., Aslanger A. D., Kardelen Al A. D., et al.

9. 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.

10. 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.

11. 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.

12. 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)

13. 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)

14. 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)

15. 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)

16. 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)

17. 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)

18. 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)

19. 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)

20. 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)

21. 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)

22. 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)

23. 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)

24. 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)

25. 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)

26. 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)

27. 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)

28. 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)

29. 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)

30. 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)

31. 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)

32. 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)

33. 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)

34. 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)

35. 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)

36. 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)

37. 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)

38. 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)

39. Identification of obesity-related genetic variants in a family with an exclusively breastfed obese infant

Çelebioğlu H. B., Ozturk A. P., Poyrazoğlu Ş., Tuncer Kılınç F. N.

56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, England, 10 - 13 June 2023, pp.162, (Summary Text)

40. 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)

41. 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

42. 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

43. Evaluation of Clinical and Laboratory Findings of Papillary Thyroid Carcinoma Patients Diagnosed in Childhood

İnan Balcı E., Poyrazoğlu Ş.

45. PEDİATRİ GÜNLERİ, İstanbul, Turkey, 25 - 28 April 2023, pp.181-183, (Full Text) Sustainable Development

44. 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)

45. 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)

46. 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)

47. 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)

48. 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)

49. 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)

50. 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)

51. 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)

52. 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)

53. 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)

54. 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)

55. 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)

56. 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)

57. 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)

58. 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)

59. Differentiated Thyroid Carcinoma with Thyroid Dysfunction in Our Cases

İnan Balcı E., Poyrazoğlu Ş.

4. PEDİATRİ GÜNLERİ 23. PEDİATRİ HEMŞİRELİĞİ GÜNLERİ, İstanbul, Turkey, 17 - 20 April 2022, pp.499-500, (Full Text)

60. 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)

61. 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)

62. 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)

63. 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)

64. 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)

65. 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)

66. 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)

67. 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)

68. 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)

69. 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)

70. 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)

71. 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)

72. 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)

73. 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)

74. 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)

75. 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)

76. 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)

77. 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)

78. 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)

79. 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)

80. 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)

81. 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)

82. 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

83. 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)

84. 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)

85. 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)

86. 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)

87. 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)

88. 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)

89. 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

90. 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)

91. **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)

92. 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)

93. 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)

94. 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)

95. 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)

96. 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)

97. 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)

98. Diagnostic contribution of in house designed next generation sequencing panel gene test for Disorders of Sexual Development from Turkey

Aghayev A., Toksoy G., Poyrazoglu S., Karaman B., Avci S., Abali Z. Y., et al.

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.79-80, (Summary Text)

99. 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)

100. 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)

101. 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)

102. 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)

103. 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

104. 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

105. 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)

106. 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)

107. 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)

108. 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)

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

Poyrazoğlu Ş., Toksoy G., Aghayev A., KARAMAN B., Şahin A., Altunoğlu U., et al.

. 57th Annual Meeting of the European Society for Paediatric Endocrinology, Atina, Greece, 27 - 29 September 2018, pp.560, (Full Text)

110. 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)

111. 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)

112. 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)

113. 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)

114. 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)

115. 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)

116. 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)

117. 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)

118. 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)

119. 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)

120. 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)

121. 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)

122. 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)

123. 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)

124. 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)

125. 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)

126. 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)

127. 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)

128. 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)

129. 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)

130. 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)

131. 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

132. 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

133. 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

134. 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)

135. 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)

136. 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)

137. 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)

138. 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)

139. 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)

140. 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

141. 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

142. Tiroid ince iğne aspirasyon biyopsinin çocuklardaki tiroid nodüllerinin takip ve tedavisindeki rolü

YILMAZ C., GENENŞ M., ÖZLÜK M. Y., EROL O. B., YAVAŞ ABALI Z., POYRAZOĞLU Ş., et al.

38. Pediatri Günleri ve 17. Pediatri Hemşireliği Günleri, Turkey, 3 - 06 April 2016

143. Çocuklarda Obezite Ve İdrar Bisfenol A Düzeyleri

GÜMÜŞ S., KILIÇ A., VARKAL M. A., YILDIZ İ., POYRAZOĞLU Ş., BAŞ F., et al.

38. Pediatri Günleri ve 17. Pediatri Hemşireliği Günleri kongresi, İstanbul, Turkey, 3 - 06 April 2016, (Full Text)

144. Erken ergenlik bulguları ile araştırılan olguda primer hipotiroidizm ve hipofizde kitle görünümü

YILDIZ M., YAVAŞ ABALI Z., GENENŞ M., POYRAZOĞLU Ş., BAŞ F., BUNDAK R., et al.

38. Pediatri Günleri ve 17. Pediatri Hemşireliği Günleri, Turkey, 3 - 06 April 2016

145. Turner sendromunda ultrasonografi ile hepatik değerlendirme kesitsel bir çalışma

YAVAŞ ABALI Z., YAVUZ E., EROL O. B., GENENŞ M., POYRAZOĞLU Ş., BAŞ F., et al.

38. Pediatri Günleri ve 17. Pediatri Hemşireliği Günleri, Turkey, 3 - 06 April 2016

146. Çocuklarda Obezite Ve İdrar Bisfenol A Düzeyleri

Gümüş S., KILIÇ A., Varkal M. A., Varkal M. A., Yıldız İ., POYRAZOĞLU Ş., et al.

38. Pediatri günleri ve 17. Hemşirelik haftası, İstanbul, Turkey, 3 - 06 April 2016

147. Osteoporoz psödoglioma sendromu

SAPMAZ S., YAVAŞ ABALI Z., GENENŞ M., ALTUNOĞLU U., POYRAZOĞLU Ş., BAŞ F., et al.

38. Pediatri Günleri ve 17. Pediatri Hemşireliği Günleri, Turkey, 3 - 06 April 2016

148. Nonklasik konjenital adrenal hiperplazi hastalarının genotip ve fenotip özellikleri

Abalı S., Akcan N., Toksoy G., Baş F., Güran T., Atay Z., et al.

38. Pediatri Günleri ve 17. Pediatri Hemşireliği Günleri, İstanbul, Turkey, 3 - 06 April 2016, vol.1, no.1, pp.95, (Summary Text)

149. Can Mycoplasma Pneumoniae Be A Trigger For Type 1 Diabetes?

Hızlı Demirkale Z., Poyrazoğlu Ş., Baş F., Ağaçfidan A., Darendeliler F. F., Somer A.

1st CONGRESS of the EUROPEAN YOUNG PAEDIATRICIANS’ ASSOCIATION, İstanbul, Turkey, 4 - 06 December 2015, pp.122, (Summary Text) Sustainable Development

150. Association Between Urinary Bisphenol A Levels And Body Weight Among Children In Our Clinic

Gümüş S., KILIÇ A., Çok İ., Battal D., Poyrazoğlu Ş., Darendeliler F.

1st CONGRESS of the EUROPEAN YOUNG PAEDIATRICIANS’ ASSOCIATION, İstanbul, Turkey, 4 - 06 December 2015, pp.109, (Full Text)

151. The evaluation of AR and SRD5A2 gene mutations in 87 patients with 46 XY DSD children in Turkey

Akcan N., Toksoy G., UYGUNER Z. O., Saka N., Altunoğlu U., Genens M., et al.

54th Annual Meeting of the ESPE, Barcelona, Spain, 1 - 03 October 2015, no.1

152. Does applying regular questionnaire to patients on GH increase the compliance

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

54 rd Annual Meeting of the European Society for Paediatric Endocrinology, 30 September - 03 October 2015, vol.84, pp.463

153. The role of thyroid fine needle aspiration cytology in the treatment and follow up of thyroid nodules in the paediatric population

GENENŞ M., YILMAZ C., ÖZLÜK M. Y., EROL O. B., YAVAŞ ABALI Z., POYRAZOĞLU Ş., et al.

54 rd Annual Meeting of the European Society for Paediatric Endocrinology, 30 September - 03 October 2015, vol.84, pp.571

154. Metabolic syndrome frequency in longitudinally followed children with prematüre adrenarche during pubertal ages

KAYA G., POYRAZOĞLU Ş., EROL O., BAŞ F., BUNDAK R., DARENDELİLER F. F.

54 rd Annual Meeting of the European Society for Paediatric Endocrinology, 30 September - 03 October 2015, vol.84, pp.84

155. CYP11B1 gene mutations in patients congenital adrenal hyperplasia in Turkey

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

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 30 September - 03 October 2015, vol.84, no.1, pp.315, (Summary Text)

156. Multiple Pituitary Hormone Deficiency Associated with Pituitary Hyperplasia: A Case Repor

Genenş M., Akcan N., Yavaş Abalı Z., Baş F., Uyguner Z. O., Poyrazoğlu Ş., et al.

1.Ege Endocrinology and Genetic Symposium, İstanbul, Turkey, 25 - 27 February 2015, vol.7, no.56, pp.81, (Summary Text)

157. CYP21A2 gene aberrations in patients with non classical congenital adrenal hyperplasia

Akcan N., UYGUNER Z. O., Toksoy G., BAŞ F., Altunoğlu U., POYRAZOĞLU Ş., et al.

Endocrine Society’s 97th Annual Meeting and Expo, San Diego, United States Of America, 5 - 08 March 2015, no.1

158. Obesity At what age does obesity the disease of the 21st Century starts

KÜÇÜKEMRE AYDIN B., DEVECİOĞLU E., KISABACAK S., GÖKÇAY E. G., BAŞ F., POYRAZOĞLU Ş., et al.

The Endocrine Society’s 97th Annual Meeting, 5 - 08 March 2015

159. CYP21A2 gene aberrations in patıents with nonclassical congenital adrenal hyperplasia

AKCAN N., UYGUNER Z. O., TOKSOY G., BAŞ F., ALTUNOĞLU U., POYRAZOĞLU Ş., et al.

The Endocrine Society’s 97th Annual Meeting, 5 - 08 March 2015

160. Genotype and phenotype charasterictics of patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

AKCAN N., UYGUNER Z. O., TOKSOY G., KARAKILIÇ ÖZTURAN E., AYDIN B., BAŞ F., et al.

53 rd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Dublin, Ireland, 18 - 20 September 2014, vol.82, no.1, pp.176-177, (Summary Text)

161. Pediatrik yaş grubunda differansiye tiroid kanseri olgularının RAİ tedavi sonuçlarının retrospektif değerlendirilmesi

ALÇIN G., ŞANLI Y., POYRAZOĞLU Ş., KUYUMCU S., ÖZKAN Z. G., YILMAZ E., et al.

26. Ulusal Nükleer Tıp Kongresi, Turkey, 16 - 20 April 2014, pp.23

162. Joubert sendromu tanılı olguda çoğul hipofiz hormon eksikliği

Akcan Tombalak N., Altunoğlu U., Toksoy G., Poyrazoğlu Ş., Uyguner Z. O., Baş F., et al.

Çocuk Endokrinolojisi Olgu Sunumları-6, , 2014, İzmir, Turkey, 18 - 19 April 2014, vol.1, no.1, pp.6, (Summary Text)

163. Yirmi Yaş Altı Papiller Tiroid Kanserli Hastalarda Tanı Anında Klinik Özellikler ve Prognoz

MERİÇ S., Memişoğlu E., SORMAZ İ. C., TUNCA F., Poyrazoğlu Ş., Baş F., et al.

19. Ulusal Cerrahi Kongresi, Antalya, Turkey, 16 - 20 April 2014, pp.171, (Summary Text) Sustainable Development

164. A case of rapid-onset obesity with hypothalamic dysfunction, hypoventilation, autonomic dysregulation: ROHHAD syndrome

UÇAR A., BAŞ F., UMUR Ö., YILMAZ Y., POYRAZOĞLU Ş., BUNDAK R., et al.

9th Joint Meeting of Pediatric Endocrinology, Milan, Italy, 19 - 22 September 2013, vol.80, pp.241, (Summary Text)

165. Gestasyon Yaşına Uygun Doğan Prematür Adrenarşlı Kızlarda Pelvis Ultrasonografi Bulguları İle Hormonal Ölçümler Ve Metabolik Parametreler Arasında İlişki Varlığının Değerlendirilmesi

UÇAR A., EROL O. B., YEKELER E., YILDIZ İ., SAKA N., BOZLAK S., et al.

35. Pediatri Günleri ve 14. Pediatri Hemşireliği Günleri, İstanbul, Turkey, 9 - 12 April 2013, (Summary Text)

166. Obezite nedeni ile başvuran bir olguda Kabuki make up sendromu ve büyüme hormonu eksikliği

UÇAR A., BAŞ F., POYRAZOĞLU Ş., KAYSERİLİ KARABEY H., Saka N., BUNDAK R., et al.

35. Pediatri günleri ve 14. pediatri hemşireliği gün leri, Turkey, 9 - 12 April 2013 Sustainable Development

167. Graves Hastalığı olan Adolesanda Metimazole Bağlı Nadir Geç Dönem Yan Etki Nötropeni

KARAASLAN F., DİNÇ B., BAŞ F., KARAMAN S., AYDIN B., UÇAR A., et al.

35. Pediatri Günleri 14. Pediatri Hemşireliği Günleri, İstanbul, Turkey, 9 - 12 April 2013, pp.315

168. Çocuk ve ergenlerde haşitoksikoz ve Graves hastalığı vakalarının otoimmun tiroid hastalıkları yelpazesi içindeki yerinin değerlendirilmesi.

GÜNEŞ D., Satan A., UÇAR A., BAŞ F., DARENDELİLER F. F., POYRAZOĞLU Ş., et al.

XVI. Ulusal Pediatrik Endokrin ve Diyabet Kongresi, Samsun, Turkey, 6 - 10 November 2012, pp.218, (Summary Text)

169. Glucocorticoid receptor gene polymorphisms and their relation with glucocorticoid sensitivity and obesity in patients with congenital adrenal hyperplasia

nurçin s., POYRAZOĞLU Ş., SAYİTOĞLU M., ÖZBEK U., Şen N., AKIN L., et al.

8.th joint meeting global care in pediatric endocrinology, New York, United States Of America, 9 - 12 September 2009

170. Yenidoğan döneminde geçici diyabet ve lipoprotein lipaz eksikliği

POYRAZOĞLU Ş., YILDIZ İ., GÜNÖZ H., GÜNDOĞDU S., GÖKÇAY G. F.

28. Pediatri Günleri ve 7. Pediatri Hemşireliği Günleri, İstanbul, Turkey, 18 April 2006, vol.6, (Full Text)

171. Response to tetanus toxoid, conjugated and unconjugated polysaccarides vaccines after paediatric allogeneic stem cell transplantation

YALMAN N., Bilgen H., Isik N., Agirbasli H., Poyrazoglu S., Anak S., et al.

31st Annual Meeting of the European-Group-for-Blood-and-Marrow-Transplantation/21st Meeting of the EBMT-Nurses-Group/4th Meeting of the EBMT-Data-Management-Group, Prague, Czech Republic, 20 - 23 March 2005, vol.35, (Summary Text)

172. Hyper immunoglobulin M sendromu: İki olgu sunumu.

Somer A., Kayserili H., Yalçın I., Salman N., Poyrazoğlu Ş., Durandy A., et al.

15.Ulusal İmmünoloji Kongresi, Antalya, Turkey, 13 - 16 October 1999, pp.29, (Summary Text)

173. X-linked hyperimmunoglobulin M syndrome: a case report.

Somer A., Yalçın I., Salman N., Poyrazoğlu Ş., Kayserili H., Kılıç G., et al.

Vth Regional Congress of Pediatric Societies of Turkish Speaking Countries with International Participation, Bishkek, Kyrgyzstan, 25 - 28 September 1999, pp.95, (Summary Text)

Books 22

Other Publications 1

1. Differansiye tiroid kanserli hastaların klinik ve patolojik özellikleri ve tedavilerinin değerlendirilmesi

POYRAZOĞLU Ş., SAKA H. N., BAŞ F., BUNDAK R., DARENDELİLER F. F.

Presentation, pp.99, 2013 Sustainable Development

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