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Scientific Reports|September 15, 2021
Unique clinical features and long term follow up of survivors of sudden cardiac death in an Asian multicenter studyPang-Shuo Huang, Jen-Fang Cheng, Wen-Chin Ko, et al.American Heart Journal|September 14, 2002
Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillationLing-Ping Lai, Ming-Jai Su, Huei-Ming Yeh, et al.Cardiology|April 25, 2003
Electrophysiological mapping and histological examinations of the swine atrium with sustained (> or =24 h) atrial fibrillation: a suitable animal model for studying human atrial fibrillationJiunn-Lee Lin, Ling-Ping Lai, Chih-Shen Lin, et al.Medicine|January 27, 2015
Effects of angiotensin converting enzyme inhibition or angiotensin receptor blockade in dialysis patients: a nationwide data survey and propensity analysisCho-Kai Wu, Yao-Hsu Yang, Jyh-Ming Jimmy Juang, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|August 2, 2024
Genetic and clinical characteristics of catecholaminergic polymorphic ventricular tachycardia in a Taiwanese nationwide cohortGrace Chia-Yen Hsu, Mei-Hwan Wu, Jing-Yuan Chuang, et al.Heart Rhythm|April 13, 2024
Predicting impaired cardiopulmonary exercise capacity in patients with atrial fibrillation using a simple echocardiographic markerHung-Jui Chuang, Lung-Chun Lin, An-Li Yu, et al.Journal of Cardiovascular Electrophysiology|March 19, 2004
Functional genomic study on atrial fibrillation using cDNA microarray and two-dimensional protein electrophoresis techniques and identification of the myosin regulatory light chain isoform reprogramming in atrial fibrillationLing-Ping Lai, Jiunn-Lee Lin, Chich-Sheng Lin, et al.International Journal of Cardiology|September 1, 2015
Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal diseaseLi-Ting Ho, Lian-Yu Lin, Yao-Hsu Yang, et al.Frontiers in Genetics|January 22, 2019
Impact of Ancestral Differences and Reassessment of the Classification of Previously Reported Pathogenic Variants in Patients With Brugada Syndrome in the Genomic Era: A SADS-TW BrS RegistryChing-Yu Julius Chen, Tzu-Pin Lu, Lian-Yu Lin, et al.European Journal of Pediatrics|September 11, 2008
Clinical spectrum and long-term outcome of Ebstein's anomaly based on a 26-year experience in an Asian cohortYa-Mei Chang, Jou-Kou Wang, Sheunn-Nan Chiu, et al.Pageof 14