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Page 1
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: ozcabi b. 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.
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: ozcabi b. 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. 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.
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: ozcabi b. 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.
Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey.
Poyrazoğlu Ş, Bundak R, Yavaş Abalı Z, Önal H, Sarıkaya S, Akgün A, Baş S, Abalı S, Bereket A, Eren E, Tarım Ö, Güven A, Yıldız M, Karaman Aksakal D, Yüksel A, Seymen Karabulut G, Hatun Ş, Özgen T, Cesur Y, Azizoğlu M, Dilek E, Tütüncüler F, Papatya Çakır E, Özcabı B, Evliyaoğlu O, Karadeniz S, Dursun F, Bolu S, Arslanoğlu İ, Yeşiltepe Mutlu G, Kırmızıbekmez H, İşgüven P, Üstyol A, Adal E, Uçar A, Cebeci N, Bezen D, Binay Ç, Semiz S, Korkmaz HA, Memioğlu N, Sağsak E, Peltek HN, Yıldız M, Akçay T, Turan S, Güran T, Atay Z, Akcan N, Çizmecioğlu F, Ercan O, Dağdeviren A, Baş F, İşsever H, Darendeliler F. Poyrazoğlu Ş, et al. Among authors: ozcabi b. J Clin Res Pediatr Endocrinol. 2018 Nov 29;10(4):336-342. doi: 10.4274/jcrpe.0025. Epub 2018 May 23. J Clin Res Pediatr Endocrinol. 2018. PMID: 29789274 Free PMC article.
Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience.
Esen İ, Bayramoğlu E, Yıldız M, Aydın M, Karakılıç Özturhan E, Aycan Z, Bolu S, Önal H, Kör Y, Ökdemir D, Ünal E, Önder A, Evliyaoğlu O, Çayır A, Taştan M, Yüksel A, Kılınç A, Büyükinan M, Özcabı B, Akın O, Binay Ç, Kılınç S, Yıldırım R, Aytaç EH, Sağsak E. Esen İ, et al. Among authors: ozcabi b. J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):164-172. doi: 10.4274/jcrpe.galenos.2018.2018.0210. Epub 2018 Nov 29. J Clin Res Pediatr Endocrinol. 2019. PMID: 30488822 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: ozcabi b. 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.
27 results