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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: bayramov r. 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
PEX10-related autosomal recessive cerebellar ataxia with hearing loss.
Kaya Özçora GD, Miyatake S, Matsumoto N, Canpolat M, Erdoğan M, Bayramov R, Kumandaş S. Kaya Özçora GD, et al. Among authors: bayramov r. Acta Neurol Belg. 2020 Apr;120(2):429-432. doi: 10.1007/s13760-018-0987-8. Epub 2018 Jul 19. Acta Neurol Belg. 2020. PMID: 30022445 No abstract available.
Dysmetabolic markers predict outcomes in autosomal dominant polycystic kidney disease.
Kocyigit I, Ozturk F, Eroglu E, Karaca Z, Kaynar AS, Cetin M, Tokgoz B, Sipahioglu MH, Bayramov R, Sen A, Oymak O, Ecder T, Axelsson J. Kocyigit I, et al. Among authors: bayramov r. Clin Exp Nephrol. 2019 Sep;23(9):1130-1140. doi: 10.1007/s10157-019-01748-z. Epub 2019 May 27. Clin Exp Nephrol. 2019. PMID: 31134465
16 results