Diagnostic and therapeutic strategies for arrhythmogenic right ventricular dysplasia/cardiomyopathy patient

Author:

Wang Weijia1,James Cynthia A1,Calkins Hugh1

Affiliation:

1. Division of Cardiology, Department of Medicine, Johns Hopkins University, 600 N. Wolfe Street, Sheikh Zayed Tower 7125R, Baltimore, MD, USA

Funder

Clinical Research Award

Dr. Francis P. Chiaramonte Private Foundation

St. Jude Medical Foundation

Boston Scientific Corp.

Leducq foundation – RHYTHM Network

la Erkan Family Fund for ARVD Research

Bogle Foundation

Healing Hearts Foundation

Peter French Memorial Foundation

Wilmerding Endowments

Foundation Leducq

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference144 articles.

1. Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement;Corrado;Eur Heart J,2015

2. Right ventricular dysplasia: a report of 24 adult cases;Marcus;Circulation,1982

3. Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression;Sen-Chowdhry;Circulation,2007

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