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Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty.
Aycan Z, Savaş-Erdeve Ş, Çetinkaya S, Kurnaz E, Keskin M, Muratoğlu Şahin N, Bayramoğlu E, Ceylaner G. Aycan Z, et al. Among authors: cetinkaya s. J Clin Res Pediatr Endocrinol. 2018 Jul 31;10(3):223-229. doi: 10.4274/jcrpe.5506. Epub 2018 Feb 28. J Clin Res Pediatr Endocrinol. 2018. PMID: 29537379 Free PMC article.
Antimüllerian Hormone Levels of Infants with Premature Thelarche.
Muratoğlu Şahin N, Bayramoğlu E, Nursun Özcan H, Kurnaz E, Keskin M, Savaş-Erdeve Ş, Çetinkaya S, Aycan Z. Muratoğlu Şahin N, et al. Among authors: cetinkaya s. J Clin Res Pediatr Endocrinol. 2019 Sep 3;11(3):287-292. doi: 10.4274/jcrpe.galenos.2019.2018.0293. Epub 2019 Mar 12. J Clin Res Pediatr Endocrinol. 2019. PMID: 30859797 Free PMC article.
Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation.
Bayramoğlu E, Şavaş Erdeve Ş, Shi Y, Keskin M, Çetinkaya S, Kurnaz E, Muratoğlu Şahin N, Aycan Z. Bayramoğlu E, et al. Among authors: cetinkaya s. J Pediatr Endocrinol Metab. 2019 Jun 26;32(6):647-651. doi: 10.1515/jpem-2018-0399. J Pediatr Endocrinol Metab. 2019. PMID: 31141481
304 results