Yazar "Bircan, Rıfat" için Fakülteler listeleme
-
The Mitochondrial DNA Control Region Might Have Useful Diagnostic and Prognostic Biomarkers for Thyroid Tumors
Bircan, Rıfat; Ilıksu Gözü, Hülya; Ulu, Esra; Sarıkaya, Şükran; Gül, Aylin Ege; Şirin, Duygu Yaşar; Aral, Cenk (Johann Ambrosius Barth Verlag Medizinverlage Heidelberg Gmbh, 2019)The literature suggests that mitochondrial DNA (mtDNA) defects are associated with a large number of diseases including cancers. The role of mtDNA variations in thyroid cancer is a highly controversial topic. Therefore, ... -
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 ... -
TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review
Kayas, Leman; Camtosun, Emine; Akıncı, Ayşehan; Bircan, Rıfat (Galenos Yayincilik, 2022)An activating variant of the thyroid stimulating hormone receptor (TSHR) gene is one of the rare causes of neonatal hyperthyroidism. This disorder may occur as a result of an autosomal dominant inheritance or sporadically ...