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Page 1
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.
Farooqi IS, Wangensteen T, Collins S, Kimber W, Matarese G, Keogh JM, Lank E, Bottomley B, Lopez-Fernandez J, Ferraz-Amaro I, Dattani MT, Ercan O, Myhre AG, Retterstol L, Stanhope R, Edge JA, McKenzie S, Lessan N, Ghodsi M, De Rosa V, Perna F, Fontana S, Barroso I, Undlien DE, O'Rahilly S. Farooqi IS, et al. Among authors: o rahilly s, ercan o. N Engl J Med. 2007 Jan 18;356(3):237-47. doi: 10.1056/NEJMoa063988. N Engl J Med. 2007. PMID: 17229951 Free PMC article.
Variable phenotypes associated with aromatase (CYP19) insufficiency in humans.
Lin L, Ercan O, Raza J, Burren CP, Creighton SM, Auchus RJ, Dattani MT, Achermann JC. Lin L, et al. Among authors: ercan o. J Clin Endocrinol Metab. 2007 Mar;92(3):982-90. doi: 10.1210/jc.2006-1181. Epub 2006 Dec 12. J Clin Endocrinol Metab. 2007. PMID: 17164303 Free PMC article.
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: ercan o. 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.
Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation.
Evliyaoğlu O, Ercan O, Ataoğlu E, Zübarioğlu Ü, Özcabı B, Dağdeviren A, Erdoğan H, De Franco E, Ellard S. Evliyaoğlu O, et al. Among authors: ercan o. J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):168-174. doi: 10.4274/jcrpe.5162. Epub 2017 Sep 25. J Clin Res Pediatr Endocrinol. 2018. PMID: 28943513 Free PMC article.
The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children.
Guran T, Turan S, Bereket A, Akcay T, Unluguzel G, Bas F, Gunoz H, Saka N, Bundak R, Darendeliler F, Isguven P, Yildiz M, Adal E, Sarikaya S, Baygin LA, Memioglu N, Onal H, Ercan O, Haklar G. Guran T, et al. Among authors: ercan o. Eur J Pediatr. 2009 Sep;168(9):1043-8. doi: 10.1007/s00431-008-0876-x. Epub 2008 Nov 29. Eur J Pediatr. 2009. PMID: 19043735
Thyroid Hormone Resistance in children.
Ercan O. Ercan O. Pediatr Endocrinol Rev. 2003 Dec;1 Suppl 2:191-8; discussion 198. Pediatr Endocrinol Rev. 2003. PMID: 16444158 Review.
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: ercan o. 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.
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome.
Dağdeviren Çakır A, Baş F, Akın O, Şıklar Z, Özcabı B, Berberoğlu M, Kardelen AD, Bayramoğlu E, Poyrazoğlu Ş, Aydın M, Törel Ergür A, Gökşen D, Bolu S, Aycan Z, Tüysüz B, Ercan O, Evliyaoğlu O. Dağdeviren Çakır A, et al. Among authors: ercan o. J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):308-319. doi: 10.4274/jcrpe.galenos.2021.2020.0228. Epub 2021 Feb 10. J Clin Res Pediatr Endocrinol. 2021. PMID: 33565750 Free PMC article.
Evaluation of the thyroid disorders in children with familial Mediterranean fever.
Turan H, Yildiz M, Civan O, Cakir AD, Tarcin G, Ozer Y, Bayramli Z, Kucur M, Adaletli I, Adrovic A, Barut K, Ercan O, Kasapcopur O, Evliyaoglu SO. Turan H, et al. Among authors: ercan o. Clin Rheumatol. 2021 Apr;40(4):1473-1478. doi: 10.1007/s10067-020-05430-8. Epub 2020 Sep 30. Clin Rheumatol. 2021. PMID: 32996072
159 results