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Heart Rhythm|August 14, 2012
Repeat long QT syndrome genetic testing of phenotype-positive cases: prevalence and etiology of detection missesMorgan M Medlock, David J Tester, Melissa L Will, 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.
Biochemical and Biophysical Research Communications|November 23, 2006
Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytesSandro L Yong, Ying Ni, Teng Zhang, et al.
Circulation. Cardiovascular Genetics|August 13, 2011
Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndromeDavid J Tester, Bi-Hua Tan, Argelia Medeiros-Domingo, et al.
Circulation|October 7, 2004
Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromesGrace Choi, Laura J Kopplin, David J Tester, et al.
Heart Rhythm|May 3, 2008
Prevalence of early-onset atrial fibrillation in congenital long QT syndromeJonathan N Johnson, David J Tester, James Perry, et al.
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