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Circulation. Arrhythmia and Electrophysiology|February 20, 2025
Characteristics of Patients With the Arrhythmogenic Mitral Valve Prolapse Syndrome and Sudden Cardiac Arrest and Sustained Ventricular ArrhythmiasApurba Chakrabarti, John R Giudicessi, Fatima M Ezzeddine, et al.
Medrxiv : the Preprint Server for Health Sciences|February 19, 2024
Multiplexed Assays of Variant Effect and Automated Patch-clamping Improve KCNH2-LQTS Variant Classification and Cardiac Event Risk StratificationMatthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, 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.
Circulation. Genomic and Precision Medicine|November 9, 2020
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A FamiliesYanushi D Wijeyeratne, Michael W Tanck, Yuka Mizusawa, et al.
JAMA Cardiology|May 17, 2023
Vigorous Exercise in Patients With Hypertrophic CardiomyopathyRachel Lampert, Michael J Ackerman, Bradley S Marino, et al.
JAMA|June 20, 2024
A Clinical Diagnostic Test for Calcium Release Deficiency SyndromeMingke Ni, Ziv Dadon, Julian O M Ormerod, et al.
JAMA|January 10, 2016
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical RecordsSara L Van Driest, Quinn S Wells, Sarah Stallings, et al.
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