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Page 1
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.
Siklar Z, Camtosun E, Bolu S, Yildiz M, Akinci A, Bas F, Dündar İ, Bestas A, Ünal E, Kocaay P, Guran T, Buyukyilmaz G, Ugurlu AK, Tosun BG, Turan I, Kurnaz E, Yuksel B, Turkkahraman D, Cayir A, Celmeli G, Gonc EN, Eklioğlu BS, Cetinkaya S, Yilmaz SK, Atabek ME, Buyukinan M, Arslan E, Mengen E, Cakir EDP, Karaoglan M, Hatipoglu N, Orbak Z, Ucar A, Akyurek N, Akbas ED, Isik E, Kaygusuz SB, Sutcu ZK, Seymen G, Berberoglu M. Siklar Z, et al. Among authors: turkkahraman d. Endocrine. 2024 Sep;85(3):1407-1416. doi: 10.1007/s12020-024-03962-6. Epub 2024 Jul 17. Endocrine. 2024. PMID: 39020240 Free PMC article.
A Large PROP1 Gene Deletion in a Turkish Pedigree.
Gorar S, Turkkahraman D, Yararbas K. Gorar S, et al. Among authors: turkkahraman d. Case Rep Endocrinol. 2018 Mar 14;2018:2403430. doi: 10.1155/2018/2403430. eCollection 2018. Case Rep Endocrinol. 2018. PMID: 30112224 Free PMC article.
CTLA-4 (+49A/G) polymorphism and type-1 diabetes in Turkish children.
Çelmeli F, Türkkahraman D, Özel D, Akçurin S, Yegin O. Çelmeli F, et al. Among authors: turkkahraman d. J Clin Res Pediatr Endocrinol. 2013;5(1):40-3. doi: 10.4274/Jcrpe.879. Epub 2013 Jul 1. J Clin Res Pediatr Endocrinol. 2013. PMID: 23367498 Free PMC article.
44 results