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Journal of Palliative Care|January 1, 1993
Victoria BGY palliative care model--a new model for the 1990sG M Downing, D L Braithwaite, J M WildeHerzschrittmachertherapie & Elektrophysiologie|February 9, 2024
Idiopathic ventricular fibrillation: is it a case for genetic testing?S N van der Crabben, A A M WildeGene|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 WildeJournal of the American College of Cardiology|July 4, 2009
Giant T-U waves precede torsades de pointes in long QT syndrome: a systematic electrocardiographic analysis in patients with acquired and congenital QT prolongationPaulus Kirchhof, Michael R Franz, Abdennasser Bardai, et al.Trends 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 BezzinaNature Reviews. Cardiology|October 5, 2019
Epidemiology of inherited arrhythmiasJoost A Offerhaus, Connie R Bezzina, Arthur A M WildePageof 73