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Heart Rhythm|September 21, 2010
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillationDaniel C Bartos, Sabine Duchatelet, Don E Burgess, et al.
The Annals of Thoracic Surgery|April 28, 2023
Septal Myectomy Outcomes in Children and Adolescents With Obstructive Hypertrophic CardiomyopathyElaine M Griffeth, Joseph A Dearani, Hartzell V Schaff, et al.
Mayo Clinic Proceedings|November 6, 2016
Incidence and Etiology of Sudden Cardiac Arrest and Death in High School Athletes in the United StatesKimberly G Harmon, Irfan M Asif, Joseph J Maleszewski, et al.
Pharmacogenomics|February 15, 2012
Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health recordAndrea H Ramirez, Yaping Shi, Jonathan S Schildcrout, et al.
Journal of Cardiovascular Electrophysiology|January 29, 2013
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillationDaniel C Bartos, Jeffrey B Anderson, Rachel Bastiaenen, et al.
Journal of Cardiovascular Electrophysiology|December 3, 2025
Outcomes of Ventricular Tachycardia Ablation in Cardiac Laminopathy: An Updated Systematic Review and Single-Arm Meta-AnalysisMatteo Castrichini, Iuri Ferreira Felix, Vanessa Karlinski Vizentin, et al.
Mayo Clinic Proceedings|June 6, 2008
Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathyIacopo Olivotto, Francesca Girolami, Michael J Ackerman, et al.
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