Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy
Authors:
- John P. VeinotJVJohn P. Veinot
- Julie RutbergJRJulie Rutberg
- Michael H. GollobMGMichael H. Gollob
- 1 September 2010
- journal article
- case report
- Published by Elsevier in Cardiovascular Pathology
- Vol. 19 (5) , 316-320
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Mechanisms of Disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathyNature Clinical Practice Cardiovascular Medicine, 2008
- A PRKAG2 mutation causes biphasic changes in myocardial AMPK activity and does not protect against ischemiaBiochemical and Biophysical Research Communications, 2007
- Adipositas cordis, fatty infiltration of the right ventricle, and arrhythmogenic right ventricular cardiomyopathy. Just a matter of fat?Cardiovascular Pathology, 2005
- β-Catenin accumulates in intercalated disks of hypertrophic cardiomyopathic heartsCardiovascular Research, 2003
- Identification of a Gene Responsible for Familial Wolff–Parkinson–White SyndromeNew England Journal of Medicine, 2001
- The Molecular Genetic Basis for Hypertrophic CardiomyopathyJournal of Molecular and Cellular Cardiology, 2001
- Inhibition of Adipogenesis by Wnt SignalingScience, 2000
- Dealing with energy demand: the AMP-activated protein kinaseTrends in Biochemical Sciences, 1999
- Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology.Heart, 1994
- Right Ventricular Cardiomyopathy and Sudden Death in Young PeopleNew England Journal of Medicine, 1988