Familial dilated cardiomyopathy

Known as: CMPD1, Cardiomyopathy, Familial Dilated, 1, FDC 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2018
051019842018

Papers overview

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2010
2010
OBJECTIVES We sought to further define the role of sarcomere mutations in dilated cardiomyopathy (DCM) and associated clinical… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Lamin A/C mutations are a well-established cause of dilated cardiomyopathy (DCM), although their frequency has not… (More)
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2004
Highly Cited
2004
LMNA mutations have been associated with familial or sporadic dilated cardiomyopathy (DC), with or without conduction system… (More)
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2001
2001
BACKGROUND Familial dilated cardiomyopathy (FDCM) and hypertrophic cardiomyopathy (FHCM) are the 2 most common forms of primary… (More)
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1999
1999
A novel dilated cardiomyopathy (DCM) in 12 related Portuguese Water Dogs was identified by retrospective analysis of postmortem… (More)
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Highly Cited
1999
Highly Cited
1999
OBJECTIVES This study was performed to evaluate the characteristics, mode of inheritance and etiology of familial dilated… (More)
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1998
Highly Cited
1998
OBJECTIVES This study sought to determine whether early disease is identifiable in asymptomatic relatives of patients with… (More)
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1997
1997
Inherited cardiomyopathies may arise from mutations in genes that are normally expressed in both heart and skeletal muscle and… (More)
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1996
Highly Cited
1996
The production, survival, and function of monocytes and macrophages is regulated by the macrophage colony-stimulating factor (M… (More)
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1994
Highly Cited
1994
A human autosomal XY sex reversal locus, SRA1, associated with the skeletal malformation syndrome campomelic dysplasia (CMPD1… (More)
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