Right ventricular cardiomyopathy

Known as: Cardiomyopathy, esp. right ventricular, Cardiomyopathy, right ventricular 
Right ventricular dysfunction (global or regional) with functional and morphological right ventricular abnormalities, with or without left… (More)
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
There have been major advances in recent years in the clinical setting of arrhythmogenic right ventricular cardiomyopathy… (More)
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Highly Cited
2012
Highly Cited
2012
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an infrequently diagnosed condition with a high incidence of sudden… (More)
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Highly Cited
2010
Highly Cited
2010
BACKGROUND In 1994, an International Task Force proposed criteria for the clinical diagnosis of arrhythmogenic right ventricular… (More)
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Review
2005
Review
2005
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease that may result in arrhythmia, heart… (More)
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Highly Cited
2004
Highly Cited
2004
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is associated with fibrofatty replacement of cardiac myocytes, ventricular… (More)
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Highly Cited
2001
Highly Cited
2001
Arrhythmogenic right ventricular dysplasia type 2 (ARVD2, OMIM 600996) is an autosomal dominant cardiomyopathy, characterized by… (More)
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Highly Cited
2000
Highly Cited
2000
BACKGROUND Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an autosomal dominant heart muscle disorder that causes… (More)
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Highly Cited
1997
Highly Cited
1997
OBJECTIVES The aim of the present investigation was to redefine the clinicopathologic profile of arrhythmogenic right ventricular… (More)
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Highly Cited
1996
Highly Cited
1996
BACKGROUND Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a frequent cause of sudden death in young individuals and… (More)
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Highly Cited
1988
Highly Cited
1988
From 1979 to 1986, we conducted postmortem studies of 60 persons under 35 years of age who had died suddenly in the Veneto Region… (More)
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