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Indian Pacing and Electrophysiology Journal|July 24, 2025
Inherited arrhythmia syndromes - CardiogeneticsFenna Tuijnenburg, Ahmad S Amin, Arthur A M WildeJournal of the American College of Cardiology|February 2, 2010
The response of the QT interval to the brief tachycardia provoked by standing: a bedside test for diagnosing long QT syndromeSami Viskin, Pieter G Postema, Zahurul A Bhuiyan, et al.Circulation|October 10, 2022
Arrhythmogenic Effects of Cardiac MemorySami Viskin, Ehud Chorin, Arie Lorin Schwartz, et al.Journal of Electrocardiology|August 27, 2021
Arrhythmic storm from ischemic ventricular fibrillation treated with intravenous quinidineEhud Chorin, Raphael Rosso, Dana Viskin, et al.Gene|September 13, 2015
The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiologyChristiaan C Veerman, Arthur A M Wilde, Elisabeth M LodderFuture Cardiology|May 14, 2010
Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heartNynke Hofman, Laura T van Lochem, Arthur A M WildeTrends in Cardiovascular Medicine|April 18, 2018
The genetic architecture of long QT syndrome: A critical reappraisalJohn R Giudicessi, Arthur A M Wilde, Michael J AckermanHeart Rhythm|July 6, 2020
Prophylactic (hydroxy)chloroquine in COVID-19: Potential relevance for cardiac arrhythmia riskJoost A Offerhaus, Arthur A M Wilde, Carol Ann RemmeHeart (British Cardiac Society)|May 27, 2021
Diagnosis, management and therapeutic strategies for congenital long QT syndromeArthur A M Wilde, Ahmad S Amin, Pieter G PostemaTrends in Cardiovascular Medicine|April 26, 2008
Cardiac sodium channel overlap syndromes: different faces of SCN5A mutationsCarol Ann Remme, Arthur A M Wilde, Connie R BezzinaPageof 60