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JACC. Clinical Electrophysiology|April 24, 2026
Trigger Type and Breakthrough Cardiac Events in Inherited Arrhythmia Syndromes After Left Cardiac Sympathetic DenervationVanessa Karlinski Vizentin, Iuri Ferreira Felix, Sahej Bains, et al.World Journal for Pediatric & Congenital Heart Surgery|February 28, 2023
Pediatric Epicardial Devices: Early and Midterm OutcomesElaine M Griffeth, Prasad Krishnan, Joseph A Dearani, et al.Heart Rhythm O2|May 2, 2022
Experiences of athletes with arrhythmogenic cardiac conditions in returning to playKayle Shapero, Chad Gier, Kaylie Briske, et al.Congenital Heart Disease|May 25, 2016
Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the YoungBrittan S Sutphin, Nicole J Boczek, Héctor Barajas-Martínez, et al.Journal of the American College of Cardiology|June 27, 2002
Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspectiveMichael J Ackerman, Sara L VanDriest, Steve R Ommen, et al.Heart Rhythm|April 19, 2017
Cardiac transplantation in children and adolescents with long QT syndromeAngela M Kelle, J Martijn Bos, Susan P Etheridge, et al.Congenital Heart Disease|July 26, 2016
Whole Exome Sequencing, Familial Genomic Triangulation, and Systems Biology Converge to Identify a Novel Nonsense Mutation in TAB2-encoded TGF-beta Activated Kinase 1 in a Child with Polyvalvular SyndromeJaeger P Ackerman, John A Smestad, David J Tester, et al.The American Journal of Cardiology|February 24, 2020
Cardiac Magnetic Resonance Imaging Features in Hypertrophic Cardiomyopathy Diagnosed at <21 Years of AgeErica D Bonura, J Martijn Bos, Mahmoud A Abdelsalam, et al.Journal of Biomedical Informatics|February 12, 2011
StarBRITE: the Vanderbilt University Biomedical Research Integration, Translation and Education portalPaul A Harris, Jonathan A Swafford, Terri L Edwards, et al.Journal of Cardiovascular Electrophysiology|August 17, 2006
Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndromeIlan Goldenberg, Arthur J Moss, Wojciech Zareba, et al.Pageof 73