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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: tosun bg. 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.
Clinical and molecular genetic characteristics of patients with hereditary hypophosphatemia.
Eltan M, Alavanda C, Abali ZY, Tosun BG, Kurt I, Kirkgoz T, Guven S, Kaygusuz SB, Abali S, Helvacioglu D, Guran T, Gokce I, Arman A, Bereket A, Ata P, Turan S. Eltan M, et al. Among authors: tosun bg. J Clin Endocrinol Metab. 2024 Dec 19:dgae868. doi: 10.1210/clinem/dgae868. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 39700445
Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency.
Boogers LS, Brüggenwirth HT, Wolffenbuttel KP, Hersmus R, Bryce J, Ahmed SF, Lucas-Herald AK, Baronio F, Cools M, Ellaithi M, Globa E, Güran T, Hiort O, Holterhus PM, MсElreavey K, Niedziela M, Stancampiano MR, Tosun BG, van Bever Y, Oosterhuis JW, Looijenga LHJ, Hannema SE. Boogers LS, et al. Among authors: tosun bg. Eur J Endocrinol. 2025 Jan 6;192(1):34-45. doi: 10.1093/ejendo/lvae154. Eur J Endocrinol. 2025. PMID: 39782875