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Page 1
Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.
Özsu E, Çetinkaya S, Bolu S, Hatipoğlu N, Savaş Erdeve Ş, Evliyaoğlu O, Baş F, Çayır A, Dündar İ, Akbaş ED, Uçaktürk SA, Berberoğlu M, Şıklar Z, Özalkak Ş, Muratoğlu Şahin N, Keskin M, Şiraz ÜG, Turan H, Öztürk AP, Mengen E, Sağsak E, Dursun F, Akyürek N, Odabaşı Güneş S, Aycan Z. Özsu E, et al. Among authors: dundar i. J Clin Res Pediatr Endocrinol. 2024 Sep 5;16(3):297-305. doi: 10.4274/jcrpe.galenos.2024.2023-10-16. Epub 2024 Apr 26. J Clin Res Pediatr Endocrinol. 2024. PMID: 38665000 Free PMC article.
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience.
Çamtosun E, Dündar İ, Akıncı A, Kayaş L, Çiftci N. Çamtosun E, et al. Among authors: dundar i. J Clin Res Pediatr Endocrinol. 2021 Feb 26;13(1):88-99. doi: 10.4274/jcrpe.galenos.2020.2020.0132. Epub 2020 Sep 17. J Clin Res Pediatr Endocrinol. 2021. PMID: 32938577 Free PMC article.
High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients.
Özer Y, Anık A, Sayılı U, Tercan U, Deveci Sevim R, Güneş S, Buhur Pirimoğlu M, Elmaoğulları S, Dündar I, Ökdemir D, Besci Ö, Jalilova A, Çiçek D, Singin B, Ulu ŞE, Turan H, Albayrak S, Kocabey Sütçü Z, Eklioğlu BS, Eren E, Çetinkaya S, Savaş-Erdeve Ş, Esen I, Demir K, Darcan Ş, Hatipoğlu N, Parlak M, Dursun F, Şıklar Z, Berberoğlu M, Keskin M, Orbak Z, Tezel B, Yürüker E, Keskinkılıç B, Kara F, Erginöz E, Darendeliler F, Evliyaoğlu O. Özer Y, et al. Among authors: dundar i. J Endocrinol Invest. 2024 Sep;47(9):2213-2224. doi: 10.1007/s40618-024-02348-9. Epub 2024 Mar 28. J Endocrinol Invest. 2024. PMID: 38546931 Free PMC article.
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: dundar i. 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.
The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.
Dundar A, Bayramov R, Onal MG, Akkus M, Dogan ME, Kenanoglu S, Cerrah Gunes M, Kazimli U, Ozbek MN, Ercan O, Yildirim R, Celmeli G, Parlak M, Dundar I, Hatipoglu N, Unluhizarci K, Akalin H, Ozkul Y, Saatci C, Dundar M. Dundar A, et al. Among authors: dundar i, dundar m. Mol Biol Rep. 2019 Aug;46(4):3677-3690. doi: 10.1007/s11033-019-04809-4. Epub 2019 Apr 20. Mol Biol Rep. 2019. PMID: 31006099
56 results