Publications & Works

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

Leucine tolerance in children with MSUD is not correlated with plasma leucine levels at diagnosis.

Kozanoǧlu T., Balcl M. C., Karaca M., Gökçay G. F.
Journal of pediatric endocrinology & metabolism : JPEM, 2022 (SCI-Expanded) identifier identifier

Risk Factors for Clinical Seizures in Neonates with Hypoxic-ischemic Encephalopathy Treated with Therapeutic Hypothermia

Bor M., Ilhan O., Karaca M., Calik M.
KLINISCHE PADIATRIE, vol.234, no.4, pp.206-214, 2022 (SCI-Expanded) identifier identifier identifier

Investigating myelin oligodendrocyte glycoprotein antibodies in hereditary citrullinemia

Oncel I., Yousefi M., İNCİ A., ARSLAN GÜLTEN Z., TEKE KISA P., Karaca M., et al.
MEDICAL HYPOTHESES, vol.160, 2022 (SCI-Expanded) identifier identifier

Cardiologic evaluation of Turkish mitochondrial fatty acid oxidation disorders

Balci M. C., Karaca M., Ergul Y., Omeroglu R. E., Demirkol M., Gokcay G. F.
PEDIATRICS INTERNATIONAL, vol.64, no.1, 2022 (SCI-Expanded) identifier identifier identifier

Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study

Bozkaya-Yilmaz S., Karadag-Oncel E., OLGAÇ DÜNDAR N., GENÇPINAR P., Sarioglu B., Arican P., et al.
EUROPEAN JOURNAL OF PEDIATRICS, vol.181, no.1, pp.383-391, 2022 (SCI-Expanded) Sustainable Development identifier identifier identifier

BTD Gene Mutations in Biotinidase Deficiency: Genotype-Phenotype Correlation

Oz O., Karaca M., Atas N., Gonel A., Ercan M.
JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN, vol.31, no.7, pp.780-785, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

Evaluation of the efficiency of serum biotinidase activity as a newborn screening test in Turkey

Ercan M., Akbulut E. D., Oz O., Atas N., Karaca M., YILMAZ F. M.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.34, no.1, pp.89-94, 2021 (SCI-Expanded) identifier identifier identifier

A rare urea cycle disorder in a neonate: N-acetylglutamate synthetase deficiency

Olgac A., Kasapkara C. S., Kilic M., Derinkuyu B. E., Azapagasi E., Kesici S., et al.
ARCHIVOS ARGENTINOS DE PEDIATRIA, vol.118, no.6, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

EVALUATION OF HEMATOLOGIC FINDINGS IN MUCOPOLYSACCHARIDOSIS CASES

Cakar N. E., Karaca M.
ACTA MEDICA MEDITERRANEA, vol.36, no.2, pp.797-800, 2020 (SCI-Expanded) identifier identifier

Investigation of alanine, propionylcarnitine (C3) and 3-hydroxyisovalerylcarnitine (C5-OH) levels in patients with partial biotinidase deficiency

Karaca M.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI, vol.44, pp.482-486, 2019 (SCI-Expanded) Creative Commons License

A novel homozygous GALC variant has been associated with Krabbe disease in a consanguineous family

Tuncer F. N., Iseri S. A. U., Yapici Z., Demir M., Karaca M., Calik M.
NEUROLOGICAL SCIENCES, vol.39, no.12, pp.2123-2128, 2018 (SCI-Expanded) identifier identifier identifier

The association between serum vitamin B-12 deficiency and tension-type headache in Turkish children

Calik M., Aktas M. S., Cecen E., Piskin I. E., Ayaydin H., Ornek Z., et al.
NEUROLOGICAL SCIENCES, vol.39, no.6, pp.1009-1014, 2018 (SCI-Expanded) identifier identifier identifier

Articles Published in Other Journals

A Newborn with Infantile-Onset Pompe Disease Improving after Administration of Enzyme Replacement Therapy: Case Report

Bor M., Ilhan O., Gumus E., Ozkan S., Karaca M.
JOURNAL OF PEDIATRIC INTENSIVE CARE, vol.11, no.01, pp.62-66, 2022 (ESCI) identifier identifier

A RARE CAUSE OF BOTH HYPO AND HYPERGLYCEMIA; GLYCOGEN STORAGE DISEASE TYPE 0: A CASE REPORT

Karaca M., Aslan H.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, vol.84, no.3, pp.454-456, 2021 (ESCI) identifier identifier

The first Turkish family with Rotor syndrome diagnosed at the molecular level

Gumus E., KARACA M., Deveci U., Jirsa M.
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, vol.55, no.4, pp.430-433, 2020 (ESCI) Sustainable Development identifier identifier identifier

Pseudohypoaldosteronism Type 1 Newborn Patient with a Novel Mutation in SCNN1B

Seyhanli M., Ilhan O., Gumus E., Bor M., Karaca M.
JOURNAL OF PEDIATRIC INTENSIVE CARE, vol.9, no.2, pp.145-148, 2020 (ESCI) identifier identifier

Specificity and sensitivity of biotinidase activity measured from dried blood spot by colorimetric method

Karaca M., Kazanasmaz H.
Annals of Medical Researc, vol.26, pp.2306-2311, 2019 (Peer-Reviewed Journal) Creative Commons License Sustainable Development

Evaluation of Echocardiographic Findings of Mucopolysaccharidosis Cases

Karaca M.
European Archives of Medical Research, vol.35, pp.167-169, 2019 (Peer-Reviewed Journal) Creative Commons License

Comparison of Phenylalanine and Tyrosine Level in Plasma and Dry Blood Drop Samples

Karaca M., Kazanasmaz H.
Türk Klinik Biyokimya Dergisi, vol.16, pp.63-71, 2018 (Peer-Reviewed Journal) Creative Commons License

Evaluation of Patients Diagnosed with Nutritional Rickets: A Single Center Study

Karaca M.
Türkiye Çocuk Hastalıkları Dergisi, vol.1, pp.46-50, 2016 (Peer-Reviewed Journal) Creative Commons License

Vitamin D Deficiency/Insufficiency in Children and Adolescents with Chronic Disease

Karaca M.
Turkish Journal of Pediatric Disease, no.4, pp.259-264, 2016 (Peer-Reviewed Journal) Creative Commons License Sustainable Development

A serious rhabdomyolysis associated with the use of quetiapine: Case report Ketiapin kullanimi ile ilişkili ciddi rabdomiyoliz

Keskin M., Ceylan G., Karaca M., Atar S., Kaçar D., Erkek N.
Turkiye Klinikleri Pediatri, vol.24, no.1, pp.32-36, 2015 (Scopus) identifier

Sepsis Tablosunda Gelen Yağ Asidi Oksidasyon Bozukluğu

EKŞİ ALP E., Oral Cebeci S., Karaca M., Ertürk T., Uysalol M., Çıtak A.
ÇOCUK DERGİSİ, vol.14, no.3, pp.125-127, 2014 (Peer-Reviewed Journal) Sustainable Development

A case of Horner's syndrome after the surgical treatment of pulmonary hydatid cyst.

Bayhan G. İ., Karaca M., Yazici Ü., Tanir G.
Turkiye parazitolojii dergisi, vol.34, pp.196-9, 2010 (Scopus) Creative Commons License identifier identifier

Refereed Congress / Symposium Publications in Proceedings

Türkiye’Deki Fenilketonüri ve Hafif Hiperfenilalaninemi Popülasyonunda PahGeninin Mutasyon Spektrumu

Karaca M., Aslanger A. D., Güleç Ç., Gedikbaşı A.
15. Ulusal Tıbbi Genetik Kongresi, Muğla, Turkey, 9 - 13 November 2022, pp.75 Creative Commons License

Canavan Hastalığından Etkilenmiş 6 Türk Olguda Klinik, Radyolojik ve Moleküler Bulgular

ASLANGER A. D., KARACA M.
2. Çocuk Medeniyeti Sempozyumu, Turkey, 8 - 10 April 2022, pp.144-147

Diagnostic Utility of Whole Exome Sequencing in patients with suspected mitochondrial disease: the single center experience in Turkish population

Gedikbaşı A., Toksoy G., Karaca M., Balcı M. C., Güleç Ç., Selamioğlu A., et al.
International Congress on Inborn Errors in Metabolism (ICIEM), Sydney, Australia, 19 - 24 November 2021, pp.1-3 Creative Commons License

Clinical and molecular features of Pompe patients: single center experience

Selamioğlu A., Karaca M., Balcı M. C., Durmuş A., Gökçay G. F.
14th International Congress of Inborn Errors of Metabolism 2021, Sydney, Australia, 21 - 24 November 2021, pp.11

Covid- 19 Pandemisinin Fenilketonüri Yenidoğan Tarama Programı Üzerine Etkileri

Selamioğlu A., Karaca M., Balcı M. C., Burmacı Can N., Gökçay G. F.
II. Uluslararası Çocuk ve Kadın Doğum kongresi, Antalya, Turkey, 21 - 24 October 2021, pp.1

Hemolitik aneminin nadir bir nedeni: İki olgu ile triozfosfat izomeraz eksikliği

Selamioğlu A., Karaca M., Balcı M. C., Gökçay G. F., Durmuş A., Pempegül Yıldız E., et al.
43. Pediatri Günleri ve 22. Pediatri Hemşireliği Günleri Toplantısı, İstanbul, Turkey, 30 May - 02 June 2021, pp.161

Mitokondriyal Hastalıklara Bütünsel Yaklaşım: Beş Aile Örneği

Gedikbaşı A., Toksoy G., Karaca M., Balcı M. C., Güleç Ç., Karaman B., et al.
14. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 20 - 22 December 2020, pp.45

Dirençli epilepsi olgularında atlanmaması gereken bir tanı: Konjenital glikozilasyon defektleri

Yıldırım B. T., Aslanger A. D., Şengenç E., Karaca M., Selamioğlu A., Yeşil Sayın G.
14. Ulusal Tıbbi Genetik Kongresi, Ankara, Turkey, 20 - 22 November 2020, pp.76 Creative Commons License

Adrenokorti̇kal yetersi̇zli̇kte ön planda akla gelmeyen di̇ğer etyoloji̇ler.

HACİŞAHİNOĞULLARI H., KOÇ M. S., MASTANZADE M., KUBAT ÜZÜM A., GÜNDÜZ T., KARACA M., et al.
38. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Turkey, 11 May 2016

Spastik diparezi ve epilepsi ile giden arginaz eksikliği olgusu

YILMAZ Y., KARACA M., BALCI M. C., SAĞLAM T., DEMİRKOL M., GÖKÇAY G. F.
37. PEDİATRİ GÜNLERİ VE 16. PEDİATRİ HEMŞİRELİĞİ GÜNLERİ, Turkey, 8 - 11 April 2015, pp.199

Books & Book Chapters

ÇOCUKLARDA NE ZAMAN METABOLİK HASTALIK DÜŞÜNELİM?

Karaca M., Gökçay G. F.
in: GENEL PEDİYATRİ-PEDİYATRİNİN TEMEL TAŞLARI, FATMA OĞUZ, Editor, EMA TIP KİTABEVİ, İstanbul, pp.789-817, 2022

Yenidoğanda Mitokondriyal Hastalıklar: Klinik ve Tanısal Bulgular

Karaca M., Gökçay G. F.
in: Yenidoğanda Nadir ve Tanı Güçlüğü Çekilen Hastalıklar - 2021, Asuman ÇELENK ÇOBAN, Editor, Türkiye Klinikleri Yayınevi, İstanbul, pp.34-39, 2021 Creative Commons License

KARACİĞER TUTULUMU İLE GİDEN GLİKOJEN DEPO HASTALIKLARI

Gökçay G. F., Karaca M.
in: Karbonhidrat Metabolizması Bozuklukları: Güncel Bir Bakış, MUSTAFA KENDİRCİ,FATİH KARDAŞ, Editor, Türkiye Klinikleri Yayınevi, İstanbul, pp.8-15, 2021 Creative Commons License

MİTOKONDRİYAL ve DİĞER ENERJİ METABOLİZMASI BOZUKLUKLARI: MİTOKONDRİYAL SOLUNUM ZİNCİRİ BOZUKLUKLARI ve BESLENME TEDAVİSİ

KARACA M., Kozanoğlu T., GÖKÇAY G. F.
in: KALITSAL METABOLİK HASTALIKLARDA BESLENME TEDAVİSİ, Eminoğlu Fatma Tuğba, Haspolat Yusuf Kenan, Çeltik Coşkun, Çarman Kürşat Bora, Akbulut Ulaş Emre, Taş Taşkın, Editor, Orient Yayınları, Ankara, pp.661-687, 2021

Covid-19 ve Doğumsal Metabolizma Hastalıkları

Durmuş A., KARACA M., BALCI M. C., SELAMİOĞLU A., Körbeyli H. K., GÖKÇAY G. F.
in: Çıocuklarda Her Yönüyle Covid-19, Demirkol Demet, Karacabey Burçin Nazlı, Karakaş Zeynep, Editor, Selen Yayıncılık, İstanbul, pp.259-268, 2021