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Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2.
Turan H, Dağdeviren Çakır A, Özer Y, Tarçın G, Özcabi B, Ceylaner S, Ercan O, Evliyaoğlu SO. Turan H, et al. Among authors: ceylaner s. J Clin Res Pediatr Endocrinol. 2021 Jun 2;13(2):232-238. doi: 10.4274/jcrpe.galenos.2020.2019.0216. Epub 2020 Jun 16. J Clin Res Pediatr Endocrinol. 2021. PMID: 32539318 Free PMC article.
Primary adrenal insufficiency caused by a novel mutation in DAX1 gene.
Evliyaoğlu O, Dokurel İ, Bucak F, Özcabı B, Ercan Ö, Ceylaner S. Evliyaoğlu O, et al. Among authors: ceylaner s. J Clin Res Pediatr Endocrinol. 2013;5(1):55-7. doi: 10.4274/Jcrpe.895. J Clin Res Pediatr Endocrinol. 2013. PMID: 23367499 Free PMC article.
Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.
Özcabı B, Tahmiscioğlu Bucak F, Ceylaner S, Özcan R, Büyükünal C, Ercan O, Tüysüz B, Evliyaoğlu O. Özcabı B, et al. Among authors: ceylaner s. J Clin Res Pediatr Endocrinol. 2015 Sep;7(3):242-8. doi: 10.4274/jcrpe.2067. J Clin Res Pediatr Endocrinol. 2015. PMID: 26831561 Free PMC article.
A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans.
Tuhan H, Ceylaner S, Nalbantoğlu Ö, Acar S, Abacı A, Böber E, Demir K. Tuhan H, et al. Among authors: ceylaner s. J Clin Res Pediatr Endocrinol. 2017 Dec 15;9(4):371-374. doi: 10.4274/jcrpe.4577. Epub 2017 Jun 30. J Clin Res Pediatr Endocrinol. 2017. PMID: 28663160 Free PMC article.
248 results