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408 results

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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: yuksel b. 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 novel homozygous nonsense NDNF variant in Kallmann syndrome.
Kotan LD, Yildiz M, Turan I, Celiloglu C, Yuksel B, Topaloglu AK. Kotan LD, et al. Among authors: yuksel b. Am J Med Genet A. 2023 Mar;191(3):831-834. doi: 10.1002/ajmg.a.63066. Epub 2022 Dec 1. Am J Med Genet A. 2023. PMID: 36454653
Different Clinical Effects of Ectodermal Dysplasias in Four Generations.
Demirhan O, Yüksel B, Yilmaz S, Cetinel N. Demirhan O, et al. Among authors: yuksel b. Actas Dermosifiliogr. 2023 Nov-Dec;114(10):918-920. doi: 10.1016/j.ad.2022.11.017. Epub 2023 Jun 3. Actas Dermosifiliogr. 2023. PMID: 37276991 Free article. English, Spanish. No abstract available.
Long-term Impact of Continuous Glucose Monitoring Assistance on Glycemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Kahramanmaraş Earthquake.
Tarçın G, Ataş N, Yaşar M, Şahin KC, Trabzon G, Dündar İ, Çiçek D, Balkı HG, Manyas H, Bitkay A, Celiloğlu C, Özdemir Dilek S, Kılıç S, Düzcan Kilimci D, Ata A, Çamtosun E, Mengen E, Karaoğlan M, Yüksel B, Uçaktürk SA. Tarçın G, et al. Among authors: yuksel b. J Clin Res Pediatr Endocrinol. 2024 Dec 23. doi: 10.4274/jcrpe.galenos.2024.2024-9-9. Online ahead of print. J Clin Res Pediatr Endocrinol. 2024. PMID: 39711017 Free article.
Different Clinical Effects of Ectodermal Dysplasias in Four Generations.
Demirhan O, Yüksel B, Yilmaz S, Cetinel N. Demirhan O, et al. Among authors: yuksel b. Actas Dermosifiliogr. 2023 Nov-Dec;114(10):T918-T920. doi: 10.1016/j.ad.2023.09.007. Epub 2023 Sep 15. Actas Dermosifiliogr. 2023. PMID: 37716501 Free article. English, Spanish. No abstract available.
POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression.
Cho HJ, Gurbuz F, Stamou M, Kotan LD, Farmer SM, Can S, Tompkins MF, Mammadova J, Altincik SA, Gokce C, Catli G, Bugrul F, Bartlett K, Turan I, Balasubramanian R, Yuksel B, Seminara SB, Wray S, Topaloglu AK. Cho HJ, et al. Among authors: yuksel b. Front Endocrinol (Lausanne). 2023 Aug 1;14:1203542. doi: 10.3389/fendo.2023.1203542. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37600690 Free PMC article.
408 results