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JACC. Clinical Electrophysiology|November 20, 2020
Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT SyndromeJeremy P Moore, Roberto G Gallotti, Kevin M Shannon, et al.
Nature Communications|November 9, 2021
The history and geographic distribution of a KCNQ1 atrial fibrillation risk alleleShannon Hateley, Angelica Lopez-Izquierdo, Chuanchau J Jou, et al.
Pediatric Cardiology|September 8, 2023
Patterns of Electrocardiographic Abnormalities in Children with Hypertrophic CardiomyopathyMayme Marshall, Aneeq Malik, Maully Shah, et al.
JACC. Clinical Electrophysiology|August 2, 2018
Life-Threatening Event Risk in Children With Wolff-Parkinson-White Syndrome: A Multicenter International StudySusan P Etheridge, Carolina A Escudero, Andrew D Blaufox, 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 4, 2017
The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registryThomas M Roston, Zhiguang Yuchi, Prince J Kannankeril, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.
JAMA Cardiology|May 17, 2023
Vigorous Exercise in Patients With Hypertrophic CardiomyopathyRachel Lampert, Michael J Ackerman, Bradley S Marino, et al.
Circulation. Arrhythmia and Electrophysiology|September 26, 2025
Intellectual and Neurodevelopmental Delays in Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: Distinct Characteristics and a More Malignant Neurocardiac PhenotypeChristina Y Miyake, Dania Kallas, Sara B Stephens, et al.
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