Arrhythmogenic Right Ventricular Cardiomyopathy: A Review of Living and Deceased Probands-Reference-Cited by-同舟云学术

Arrhythmogenic Right Ventricular Cardiomyopathy: A Review of Living and Deceased Probands

Published:2019-07 Issue:7 Volume:28 Page:1034-1041
ISSN:1443-9506
Container-title:Heart, Lung and Circulation
language:en
Short-container-title:Heart, Lung and Circulation

Author:

Blusztein David I.,Zentner Dominica,Thompson Tina,Jayadeva Pavithra,Liang Danlu,Wang Ray,Winship Ingrid,James Paul A.,Trainer Alison H.,Kalman Jonathan M.,Vohra Jitendra

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine

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5. Clinical presentation, long-term follow-up, and outcomes of 1001 arrhythmogenic right ventricular dysplasia/cardiomyopathy patients and family members. Clinical perspective;Groeneweg;Circ Cardiovasc Genet,2015

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3. Severe Right Ventricular Dysplasia with Absent Pulmonary Valve Syndrome and Tricuspid Atresia: A Literature Review;Congenital Heart Disease;2020

4. 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy;Heart Rhythm;2019-11

5. Phenotypic Manifestations of Arrhythmogenic Cardiomyopathy in Children and Adolescents;Journal of the American College of Cardiology;2019-07