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Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|October 25, 2018
Potentially modifiable factors of dofetilide-associated risk of torsades de pointes among hospitalized patients with atrial fibrillationNiyada Naksuk, Alan M Sugrue, Deepak Padmanabhan, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|January 12, 2008
Impact of septal myectomy on left atrial volume and left ventricular diastolic filling patterns: an echocardiographic study of young patients with obstructive hypertrophic cardiomyopathyShaji C Menon, Michael J Ackerman, Steve R Ommen, et al.The Annals of Thoracic Surgery|October 9, 2012
Outcome of septal myectomy for obstructive hypertrophic cardiomyopathy in children and young adultsSalah E Altarabsheh, Joseph A Dearani, Harold M Burkhart, et al.European Heart Journal. Digital Health|March 20, 2024
Artificial intelligence-enhanced electrocardiogram for arrhythmogenic right ventricular cardiomyopathy detectionIkram U Haq, Kan Liu, John R Giudicessi, et al.Heart Rhythm|April 11, 2020
Left cardiac sympathetic denervation reduces skin sympathetic nerve activity in patients with long QT syndromeJie Han, Michael J Ackerman, Christopher Moir, et al.Circulation. Genomic and Precision Medicine|August 9, 2024
Clinical Utility of Protein Language Models in Resolution of Variants of Uncertain Significance in KCNQ1, KCNH2, and SCN5A Compared With Patch-Clamp Functional CharacterizationDan Ye, Ramin Garmany, Estefania Martinez-Barrios, et al.Cardiogenetics|December 10, 2013
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotypeJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.Journal of Cardiovascular Electrophysiology|January 7, 2015
Effects on repolarization using dynamic QT interval monitoring in long-QT patients following left cardiac sympathetic denervationChristopher V Desimone, J Martijn Bos, Katy M Bos, et al.Plos One|June 29, 2017
MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathyJames W McNamara, Amy Li, Sean Lal, et al.Circulation. Cardiovascular Genetics|April 24, 2015
Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium ChannelJamie D Kapplinger, John R Giudicessi, Dan Ye, et al.Pageof 73