Yazar "Akın, Leyla" için Fakülteler listeleme
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A Novel Mutation in the MC2R Gene Causing Familial Glucocorticoid Deficiency Type 1
Akın, Mustafa Ali; Akın, Leyla; Çoban, Dilek; Öztürk, Mehmet Adnan; Bircan, Rıfat; Kurtoğlu, Selim (Karger, 2011)Familial glucocorticoid deficiency (FGD) or hereditary unresponsiveness to adrenocorticotropin (ACTH) is an autosomal recessive disorder characterized by isolated glucocorticoid deficiency associated with normal mineralocorticoid ... -
Thyroid Hormone Resistance Beta: Eighteen Pediatric Patient Experience
Şiraz, Ülkü Gül; Direk, Gül; Akın, Leyla; Bircan, Rifat; Uzan Tatlı, Zeynep; Hatipoğlu, Nihal; Kurtoğlu, Selim (Karger, 2018)[No Abstract Available]