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International Journal of Cardiology. Heart & Vasculature|February 9, 2022
Sex- and age specific association of new-onset atrial fibrillation with in-hospital mortality in hospitalised COVID-19 patientsJoost A Offerhaus, Linda P T Joosten, Maarten van Smeden, et al.Journal of the American College of Cardiology|July 19, 2005
Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhoodGertie C M Beaufort-Krol, Maarten P van den Berg, Arthur A M Wilde, et al.Journal of the American College of Cardiology|October 1, 2013
A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescenceRoos F Marsman, Julien Barc, Leander Beekman, et al.Circulation. Genomic and Precision Medicine|May 22, 2019
Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain SignificanceJohn R Giudicessi, Krystien V V Lieve, Ram K Rohatgi, et al.Circulation. Arrhythmia and Electrophysiology|March 31, 2017
Effect of Age and Sex on the QTc Interval in Children and Adolescents With Type 1 and 2 Long-QT SyndromeArja S Vink, Sally-Ann B Clur, Ronald B Geskus, et al.European Heart Journal|November 9, 2006
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?Nynke Hofman, Arthur A M Wilde, Stefan Kääb, et al.Heart Rhythm|September 1, 2009
Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)Pieter G Postema, Christian Wolpert, Ahmad S Amin, 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|August 7, 2013
Early mortality in prophylactic implantable cardioverter-defibrillator recipients: development and validation of a clinical risk scoreKarin Kraaier, Marcoen F Scholten, Jan G P Tijssen, et al.Heart Rhythm|November 19, 2021
A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndromeSahej Bains, Steven M Dotzler, Christian Krijger, et al.Molecular Genetics & Genomic Medicine|September 26, 2017
Autosomal recessive long QT syndrome, type 1 in eight families from Saudi ArabiaAmnah Y Bdier, Saleh Al-Ghamdi, Prashant K Verma, et al.Pageof 60