Exercise restriction is protective for genotype-positive family members of arrhythmogenic right ventricular cardiomyopathy patients
Author:
Affiliation:
1. Department of Medicine, Division of Cardiology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA
2. Department of Medicine, Division of Cardiology, University of Massachusetts School of Medicine, Worcester, MA, USA
Abstract
Funder
Fondation Leducq
Leonie-Wild Foundation
Dr Francis P. Chiaramonte Private Foundation
Leyla Erkan Family Fund for ARVD Research
Dr Satish, Rupal
Robin Shah ARVD Fund
Bogle Foundation
Healing Hearts Foundation
Campanella family
Patrick J. Harrison Family
Peter French Memorial Foundation
Wilmerding Endowments
Publisher
Oxford University Press (OUP)
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
http://academic.oup.com/europace/article-pdf/22/8/1270/33561037/euaa105.pdf
Reference20 articles.
1. Arrhythmogenic right ventricular cardiomyopathy;Corrado;N Engl J Med,2017
2. Clinical presentation, long-term follow-up, and outcomes of 1001 arrhythmogenic right ventricular dysplasia/cardiomyopathy patients and family members;Groeneweg;Circ Cardiovasc Genet,2015
3. Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers;James;J Am Coll Cardiol,2013
4. Vigorous physical activity impairs myocardial function in patients with arrhythmogenic right ventricular cardiomyopathy and in mutation positive family members;Saberniak;Eur J Heart Fail,2014
5. Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the North American multidisciplinary study of arrhythmogenic right ventricular cardiomyopathy;Ruwald;Eur Heart J,2015
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