Kurum Yazarı "Bircan, Rıfat" PubMed İndeksli Yayın Koleksiyonu İçin Listeleme
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High Prevalence of TSHR/Gs alpha Mutation-negative Clonal Hot Thyroid Nodules (HNs) in a Turkish Cohort
Sancak, Seda; Jaeschke, Holger; Eren, Funda; Özlem, T.; Güllüoğlu, Bahadır; Şen, L. S.; Eszlinger, Markus; Bircan, R. (Georg Thieme Verlag Kg, 2011)Whereas the majority of hot thyroid nodules are caused by somatic TSH-receptor mutations, the percentage of TSH-receptor mutation negative clonal hot nodules (HN) and thus the percentage of hot nodules likely caused by ... -
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 ...