Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Esin Karakılıç Özturan"'
Autor:
Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, Birsen Karaman, Güven Toksoy, Şükran Poyrazoğlu, Şahin Avcı, Umut Altunoğlu, Zehra Yavaş Abalı, Ayşe Pınar Öztürk, Esin Karakılıç Özturan, Seher Başaran, Feyza Darendeliler, Z. Oya Uyguner
Publikováno v:
JCRPE, Vol 15, Iss 4, Pp 338-347 (2023)
INTRODUCTION: Recent reports have indicated the role of the prokineticin receptor 2 gene (PROKR2) in the etiology of pituitary hormone deficiencies, suggesting a potential role for the PROK2 pathway in pituitary development, in addition to its role i
Externí odkaz:
https://doaj.org/article/18a4807ddfcf44a1a51a2d2bcc230afd
Autor:
Aslı Derya Kardelen, Esin Karakılıç Özturan, Şükran Poyrazoğlu, Firdevs Baş, Serdar Ceylaner, Sjoerd D. Joustra, Jan M. Wit, Feyza Darendeliler
Publikováno v:
JCRPE, Vol 15, Iss 4, Pp 431-437 (2023)
IGSF1 deficiency is a rare X-linked condition characterized by central hypothyroidism and a wide variety of other clinical features with variable prevalence, including a delayed pubertal testosterone rise and growth spurt in the context of normal or
Externí odkaz:
https://doaj.org/article/26c5c42b08f8451b819dcab51f432758
Autor:
Esin Karakılıç Özturan, Ayşe Pınar Öztürk, Firdevs Baş, Ayşe Burcu Erdoğdu, Seven Kaptan, Aslı Derya Kardelen, Şükran Poyrazoğlu, Melek Yıldız, Neşe Direk, Şahika Yüksel, Feyza Darendeliler
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 276-284 (2023)
INTRODUCTION: A significant rise in the number of trans adolescents seeking medical interventions has been reported in recent years. The aim of this study was to report the clinical features, treatment, and follow-up of adolescents with gender dyspho
Externí odkaz:
https://doaj.org/article/2d05d8ae00ae48a1adaf639a9a6d33a8
Autor:
Esin Karakılıç Özturan, Ayşe Pınar Öztürk, Firdevs Baş, Ayşe Burcu Erdoğdu, Seven Kaptan, Aslı Derya Kardelen Al, Şükran Poyrazoğlu, Melek Yıldız, Neşe Direk, Şahika Yüksel, Feyza Darendeliler
Publikováno v:
JCRPE, Vol 15, Iss 4, Pp 451-451 (2023)
Externí odkaz:
https://doaj.org/article/451711183a2541e9b26bc794d2e03eb0
Autor:
Ayşe Pınar Öztürk, Esin Karakılıç Özturan, Feryal Gün Soysal, Seher Ünal, Göknur Işık, Gülçin Yeğen, Semen Önder, Melek Yıldız, Şükran Poyrazoğlu, Firdevs Baş, Feyza Darendeliler
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 119-125 (2022)
Papillary thyroid cancer (PTC) is extremely rare in children. Herein, we present a case diagnosed with PTC at 15 months of age. We conducted a literature review of the published cases with PTC under five years of age. A 1.25-year-old male patient had
Externí odkaz:
https://doaj.org/article/30a7e65b19684ea89dc70084fb9c9de1
Autor:
Ayşe Pınar Öztürk, Aslı Dudaklı, Esin Karakılıç Özturan, Şükran Poyrazoğlu, Firdevs Baş, Feyza Darendeliler
Publikováno v:
Klinische Pädiatrie. 234:199-205
Osteogenesis imperfecta (OI) is a genetic disease characterized by fragile bones and variable short stature.We performed a retrospective cohort study to evaluate demographic data, clinical findings, growth and pubertal characteristics, and medical tr
Autor:
Aslı Derya, Kardelen, Esin, Karakılıç Özturan, Şükran, Poyrazoğlu, Firdevs, Baş, Serdar, Ceylaner, Sjoerd D, Joustra, Jan M, Wit, Feyza, Darendeliler
Publikováno v:
Journal of clinical research in pediatric endocrinology.
Autor:
Aslı Derya Kardelen, Esin Karakılıç Özturan, Şükran Poyrazoğlu, Firdevs Baş, Serdar Ceylaner, Sjoerd D Joustra, Jan M Wit, Feyza Darendeliler
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Autor:
Aslı Kardelen, Esin Karakılıç Özturan, Leyla Asgarova, Ayşe Öztürk, Melek Yıldız, Şükran Poyrazoğlu, Firdevs Baş, Fatma Darendeliler
Publikováno v:
Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi.
Publikováno v:
İstanbul Tıp Fakültesi Dergisi. 84
Gender Dysphoria (GD) is a condition which is characterized by incongruence between the experienced gender and the natal sex at least for 6-months, which also causes deterioration of functionality. After psychiatric evaluations, medical treatment for