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Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations.
Demirbilek H, Cayir A, Flanagan SE, Yıldırım R, Kor Y, Gurbuz F, Haliloğlu B, Yıldız M, Baran RT, Akbas ED, Demiral M, Ünal E, Arslan G, Vuralli D, Buyukyilmaz G, Al-Khawaga S, Saeed A, Al Maadheed M, Khalifa A, Onal H, Yuksel B, Ozbek MN, Bereket A, Hattersley AT, Hussain K, De Franco E. Demirbilek H, et al. J Clin Endocrinol Metab. 2020 Dec 1;105(12):e4351-9. doi: 10.1210/clinem/dgaa613. J Clin Endocrinol Metab. 2020. PMID: 32893856 Free PMC article.
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.
Sherif M, Demirbilek H, Çayır A, Tahir S, Çavdarlı B, Demiral M, Cebeci AN, Vurallı D, Rahman SA, Unal E, Büyükyılmaz G, Baran RT, Özbek MN, Hussain K. Sherif M, et al. J Clin Res Pediatr Endocrinol. 2021 Feb 26;13(1):34-43. doi: 10.4274/jcrpe.galenos.2020.2020.0152. Epub 2020 Sep 17. J Clin Res Pediatr Endocrinol. 2021. PMID: 32938580 Free PMC article.
The First Case of 4H Syndrome with Type 1 Diabetes Mellitus.
Buyukyilmaz G, Erozan Cavdarlı B, Toksoy Adiguzel K, Adiguzel M, Kasapkara CS, Gurbuz F, Boyraz M, Gurkas E. Buyukyilmaz G, et al. J Clin Res Pediatr Endocrinol. 2023 Mar 28. doi: 10.4274/jcrpe.galenos.2023.2023-1-15. Online ahead of print. J Clin Res Pediatr Endocrinol. 2023. PMID: 36974356 Free article.
13 results