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Mayo Clinic Proceedings|October 13, 2012
Concealed long QT syndrome and intractable partial epilepsy: a case reportJason H Anderson, Johan Martijn Bos, Fredric B Meyer, et al.The Journal of Thoracic and Cardiovascular Surgery|July 31, 2007
Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysmsStephen H McKellar, David J Tester, Marineh Yagubyan, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 25, 2020
Prevalence and electrophysiological phenotype of rare SCN5A genetic variants identified in unexplained sudden cardiac arrest survivorsJohn R Giudicessi, Dan Ye, Marissa J Stutzman, et al.Mayo Clinic Proceedings|April 12, 2005
Sarcomeric genotyping in hypertrophic cardiomyopathySara L Van Driest, Steve R Ommen, A Jamil Tajik, et al.Mayo Clinic Proceedings|June 11, 2005
Yield of genetic testing in hypertrophic cardiomyopathySara L Van Driest, Steve R Ommen, A Jamil Tajik, et al.Journal of Molecular and Cellular Cardiology|April 2, 2013
Caveolin-3 suppresses late sodium current by inhibiting nNOS-dependent S-nitrosylation of SCN5AJianding Cheng, Carmen R Valdivia, Ravi Vaidyanathan, et al.Journal of the American College of Cardiology|August 9, 2023
Fatal Cardiac Arrhythmias During Electronic Gaming in Patients With Genetically Mediated Heart DiseasesRaquel Neves, Sahej Bains, J Martijn Bos, et al.The American Journal of Cardiology|October 6, 2010
Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testingDavid J Tester, Amber J Benton, Laura Train, et al.European Heart Journal|January 9, 2021
Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway?Elijah R Behr, Yael Ben-Haim, Michael J Ackerman, et al.Mayo Clinic Proceedings|April 29, 2022
Right Ventricular Enlargement and Dysfunction Are Associated With Increased All-Cause Mortality in Hypertrophic CardiomyopathySongnan Wen, Cristina Pislaru, Steve R Ommen, et al.Pageof 73