Yazar "Tutgun Onrat, Serap" için listeleme
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Analysis of thrombophilic gene mutations in coronary artery ectasia
Yalım, Zafer; Tutgun Onrat, Serap; Emren, Sadık Volkan; Dural, İbrahim Etem; Avşar, Alaettin; Onrat, Ersel (2020)Objective: Coronary artery ectasia (CAE) is defined as localized or diffuse dilatation in the coronary artery lumen of at least 1.5 times the diameter of adjacent healthy reference segments. The etiology of CAE is still ... -
Could Aneurysm and Atherosclerosis-Associated MicroRNAs ( miR 24-1-5p, miR 34a-5p, miR 126-5p, miR 143-5p, miR 145-5p) Also Be Associated with Coronary Artery Ectasia?
Yalım, Zafer; Tutgun Onrat, Serap; Dural, İbrahim Ethem; Onrat, Ersel (NY : Mary Ann Liebert, 2023)Background: Coronary artery ectasia (CAE), known for localized or diffuse excessive dilatation of the coronary artery, has an unknown etiology, but it has been reported that the underlying cause may be atherosclerosis and ... -
The effects of genetic polymorphisms and diabetes mellitus on the development of peripheral artery disease
Yalım, Zafer; Tutgun Onrat, Serap; Alan Yalım, Sümeyra; Aldemir, Mustafa; Avşar, Alaettin; Doğan, İsmet; Onrat, Ersel (2020)Objective: Peripheral artery disease (PAD) is a condition caused by the narrowing of limb arteries due to atherosclerosis. In recent years, polymorphisms in a number of genes have been shown to contribute to the risk of ... -
Investigating changes in β-adrenergic gene expression (ADRB1 and ADRB2) in Takotsubo (stress) cardiomyopathy syndrome; a pilot study
Tutgun Onrat, Serap; Dural, İbrahim Etem; Yalım, Zafer; Onrat, Ersel (Springer, 29.10.2021)Background Takotsubo Cardiomyopathy (TC) is a rare disorder that is mostly caused by stress and is often misdiagnosed. We aimed to analyze Takotsubo Syndrome at the molecular level by using the Oxford Nanopore Minion ... -
Miyotonik Distrofi Hastalarının CTG Tekrar Sayıları ile Genotip ve Klinik Bulguların Değerlendirilmesi: Tek Merkez Deneyimi-Olgu Serisi
Tutgun Onrat, Serap; Elmas, Muhsin; Yıldırım, Ümit Can; Demirbaş, Hayri (Türkiye Klinikleri, 2021)Amaç: Miyotonik distrofi hastalığı (MD), otozomal dominant genetik geçiş özelliği gösteren, motor, psikiyatrik ve bilişsel içerikli klinik bulgularla karakterize, CTG tekrar dizisi artışıyla ilerleyici nörodejeneratif bir ...
