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Hüseyin Demirbilek (Huseyin Demirbilek)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 11

Top Venues

Journal of clinical research in pediatric endocrinology

Pediatric diabetes

The Journal of clinical endocrinology and metabolism

Journal of pediatric endocrinology & metabolism : JPEM

This page only lists publications with an associated author ORCID identifier.

Publications

Şervan Özalkak, Ruken Yıldırım, Selma Tunç, Edip Unal, Funda Feryal Taş, Hüseyin Demirbilek, Mehmet Nuri Özbek
Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report Journal of clinical research in pediatric endocrinology 14 (2) (2022)
Melek Yıldız, Emregul Isik, Zehra Yavas Abali, Mehmet Keskin, Mehmet Nuri Ozbek, Firdevs Bas, Seyit Ahmet Ucakturk, Muammer Buyukinan, Hasan Onal, Cengiz Kara, Karl-Heinz Storbeck, Feyza Darendeliler, Atilla Cayir, Edip Unal, Ahmet Anik, Hüseyin Demirbilek, Tugba Cetin, Fatma Dursun, Gonul Catli, Serap Turan, Henrik Falhammar, Tugba Baris, Ali Yaman, Goncagul Haklar, Abdullah Bereket, Tülay Güran
Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency. The Journal of clinical endocrinology and metabolism 106 (9) (2021)
Meliha Demiral, Mehmet Salih Karaca, Edip Unal, Birsen Baysal, Rıza Taner Baran, Hüseyin Demirbilek, Mehmet Nuri Ozbek
A novel diagnostic tool for the evaluation of hypothalamic-pituitary region and diagnosis of growth hormone deficiency: pons ratio. Journal of pediatric endocrinology & metabolism : JPEM 33 (6) (2020)
Meliha Demiral, Edip Unal, Birsen Baysal, Rıza Taner Baran, Hüseyin Demirbilek, Mehmet Nuri Özbek
Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-Eastern Region of Turkey Journal of clinical research in pediatric endocrinology 12 (3) (2020)
Edip Unal, Meliha Demiral, Birsen Baysal, Mehmet Ağın, Elif Gökçe Devecioğlu, Hüseyin Demirbilek, Mehmet Nuri Özbek
Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Muhammet Asena, Meliha Demiral, Edip Unal, Murat Öcal, Hüseyin Demirbilek, Mehmet Nuri Özbek
Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism Journal of clinical research in pediatric endocrinology 12 (3) (2020)
Maha Sherif, Hüseyin Demirbilek, Atilla Çayır, Sophia Tahir, Busranur Erozan Cavdarli, Meliha Demiral, Ayşe Nurcan Cebeci, Dogus Vuralli, Sofia Asim Rahman, Edip Unal, Gönül Büyükyılmaz, Rıza Taner Baran, Mehmet Nuri Özbek, Khalid Hussain
Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Meliha Demiral, Hüseyin Demirbilek, Kıymet Çelik, Nilufer Okur, Khalid Hussain, Mehmet Nuri Ozbek
Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of life. Pediatric diabetes 21 (7) (2020)
Meliha Demiral, Hüseyin Demirbilek, Edip Unal, Ceren Damla Durmaz, Serdar Ceylaner, Mehmet Nuri Özbek
Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 Gene Journal of clinical research in pediatric endocrinology 12 (3) (2019)
Emregül Işık, Hüseyin Demirbilek, Jayne A L Houghton, Sian Ellard, Sarah E. Flanagan, Khalid Hussain
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation Journal of clinical research in pediatric endocrinology 11 (1) (2018)
Hüseyin Demirbilek, Nihal Hatipoglu, Ulku Gul, Zeynep U Tatli, Sian Ellard, Sarah E. Flanagan, Elisa De Franco, Selim Kurtoglu
Permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense mutation in NEUROD1. Pediatric diabetes 19 (5) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Hüseyin Demirbilek (Huseyin Demirbilek)