Yazar "Yüksel, Uygar Çağdaş" için listeleme
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Characteristics of a large-scale cohort with accessory pathway(s): A cross-sectional retrospective study highlighting over a twenty-year experience
Görmel, Suat; Yaşar, Salim; Asil, Serkan; Bozkurt, Erhan; Fırtına, Serdar; Tolunay, Hatice; Vurgun, Veysel Kutay; Yıldırım, Erkan; Gökoğlan, Yalçın; Buğan, Barış; Çelik, Murat; Yüksel, Uygar Çağdaş; Kabul, Hasan Kutsi; Amasyalı, Basri; Barçın, Cem; Köse, Sedat (AVES Yayıncılık, 2021)Objective: Catheter ablation following electrophysiologic study (EPS) is the mainstay of diagnosis and treatment for patients with atrioventricular reentrant tachycardia (AVRT), demonstrating excellent long-term outcome ... -
The definition of sarcomeric and non-sarcomeric gene mutations in hypertrophic cardiomyopathy patients: A multicenter diagnostic study across Türkiye
Oktay, Veysel; Tüfekçioğlu, Omaç; Yılmaz, Dilek Çiçek; Onrat, Ersel; Karabulut, Dilay; Çelik, Murat; Balcıoğlu, Akif Serhat; Sucu, Mehmet Murat; Özdemir, Güllü; Kaya, Hakkı; Kış, Mehmet; Güven, Barış; Bağdatoğlu, Oktay; Turhan Çağlar, Fatma Nihan; Yüksel, Uygar Çağdaş; Düzen, İrfan Veysel; Barutçu, Ahmet; Şimşir, Özgüç Semih; Başarıcı, İbrahim; Parpur, Afşin; Dalgıç, Onur; Arıcan Özlük, Fatma Özlem; Evlice, Mert; Sağ, Saim; Deniz, Muhammed Furkan; Öcal, Arslan; Gazi, Emine; Şen, Taner; Özdabakoğlu, Osman; Bayar Çakıcı, Nermin; Bakır, Eren Ozan; Ülgen Kunak, Ayşegül; Çaylı, Gizem; Taşdelen, Aybike Gül; Akşit, Ercan; Uslu Çil, Şefika; Onay, Hüseyin (KARE publishing, 2023)Background: Hypertrophic cardiomyopathy is a common genetic heart disease and up to 40%-60% of patients have mutations in cardiac sarcomere protein genes. This genetic diagnosis study aimed to detect pathogenic or likely ...
