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Circulation|February 13, 2018
Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic TestingJohn R Giudicessi, Dan M Roden, Arthur A M Wilde, et al.
Journal of Cardiovascular Electrophysiology|September 4, 2010
Sodium channelopathies: do we really understand what's going on?Pieter G Postema, Arend Mosterd, Nynke Hofman, et al.
Heart Rhythm|August 1, 2025
Personalized sudden cardiac death risk prediction in genetic heart diseases: Beyond one-size-fits-allMyrthe Y C van der Heide, Tom E Verstraelen, Arthur A M Wilde
Journal of the American College of Cardiology|July 6, 2004
Drug-induced atrioventricular block: prognosis after discontinuation of the culprit drugDavid Zeltser, Dan Justo, Amir Halkin, et al.
Journal of the American College of Cardiology|May 28, 2011
Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardiaChristian van der Werf, Prince J Kannankeril, Frederic Sacher, et al.
Expert Opinion on Pharmacotherapy|March 4, 2008
Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overviewJeroen P P Smits, Marieke T Blom, Arthur A M Wilde, et al.
Annals of Internal Medicine|May 15, 2019
Cases in Precision Medicine: Genetic Assessment After a Sudden Cardiac Death in the FamilyRonald Laracuente, Marc Paul Waase, Isha Kalia, et al.
Trends in Cardiovascular Medicine|September 5, 2017
Effect of age and gender on the QTc-interval in healthy individuals and patients with long-QT syndromeArja Suzanne Vink, Sally-Ann B Clur, Arthur A M Wilde, et al.
Journal of the American College of Cardiology|March 12, 2011
Mandatory electrocardiographic screening of athletes to reduce their risk for sudden death proven fact or wishful thinking?Arie Steinvil, Tamar Chundadze, David Zeltser, et al.
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