Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Aslı Derya Kardelen Al"'
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:
Hülya Yılmaz Aydoğan, Sukran Poyrazoglu, Ilhan Satman, Feyza Darendeliler, Kazim Yalcin Arga, Oğuz Öztürk, Gizem Gulfidan, Nurdan Gul, Deniz Kanca Demirci, Canan Cacina, Aslı Derya Kardelen Al, Yildiz Tutuncu
Publikováno v:
OMICS: A Journal of Integrative Biology. 25:431-449
Diabetes is a common disorder with a heterogeneous clinical presentation and an enormous burden on health care worldwide. About 1-6% of patients with diabetes suffer from maturity-onset diabetes of the young (MODY), the most common form of monogenic
Autor:
Ayca Dilruba Aslanger, Serdar Ceylaner, Gozde Yesil, Sukran Poyrazoglu, Firdevs Bas, Aslı Derya Kardelen Al, Feyza Darendeliler
Publikováno v:
Hormone Research in Paediatrics. 92:395-403
Introduction: Isolated adrenocorticotropic hormone (ACTH) deficiency (IAD) is a rare cause of adrenal insufficiency and T-box pituitary restricted transcription factor (TBX19) mutations are responsible for two-thirds of the neonatal onset form of the
Autor:
Aslı Derya, Kardelen Al, Şükran, Poyrazoğlu, Ayça, Aslanger, Gözde, Yeşil, Serdar, Ceylaner, Firdevs, Baş, Feyza, Darendeliler
Publikováno v:
Hormone research in paediatrics. 92(6)
Isolated adrenocorticotropic hormone (ACTH) deficiency (IAD) is a rare cause of adrenal insufficiency and T-box pituitary restricted transcription factor (TBX19) mutations are responsible for two-thirds of the neonatal onset form of the disease. IAD