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Journal of the American Heart Association|September 15, 2016
Variants in the SCN5A Promoter Associated With Various Arrhythmia PhenotypesNobue Yagihara, Hiroshi Watanabe, Phil Barnett, et al.
JACC. Clinical Electrophysiology|May 25, 2023
Functional Epicardial Conduction Disturbances Due to a SCN5A Variant Associated With Brugada SyndromeEstelle Renard, Richard D Walton, David Benoist, et al.
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
JACC. Clinical Electrophysiology|August 27, 2025
The Clinical Significance of Atrial Fibrillation in Non-High-Risk Brugada Syndrome: The BruFib StudyMarco Bergonti, Frederic Sacher, Bernard Belhassen, et al.
Circulation. Arrhythmia and Electrophysiology|December 15, 2023
Clinical Management of Brugada Syndrome: Commentary From the ExpertsMichael J Cutler, Lee L Eckhardt, Elizabeth S Kaufman, et al.
Cardiovascular Research|February 19, 2015
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative studyElijah R Behr, Eleonora Savio-Galimberti, Julien Barc, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
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