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Hypertrophic Cardiomyopathy

Known as: Cardiomyopathies, Hypertrophic Obstructive, Hypertrophic obstructive cardiomyopathy, Obstructive Cardiomyopathies, Hypertrophic 
A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Myocardial diseases are associated with an increased risk of potentially fatal cardiac arrhythmias and sudden cardiac death… Expand
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Review
2019
Review
2019
Hypertrophic cardiomyopathy (HCM) has been considered a heterogeneous cardiac disease ascribed solely to single sarcomere gene… Expand
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Highly Cited
2015
Highly Cited
2015
Your love and endless support keep me afloat. iv ACKNOWLEDGEMENTS I would like to acknowledge those whose guidance and support… Expand
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Highly Cited
2012
Highly Cited
2012
BACKGROUND Dilated cardiomyopathy and hypertrophic cardiomyopathy arise from mutations in many genes. TTN, the gene encoding the… Expand
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Hypertrophic cardiomyopathy is an autosomal-dominant disorder in which 10 genes and numerous mutations have been… Expand
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Highly Cited
2003
Highly Cited
2003
BACKGROUND The influence of left ventricular outflow tract obstruction on the clinical outcome of hypertrophic cardiomyopathy… Expand
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Highly Cited
1998
Highly Cited
1998
BACKGROUND For more than 20 years in Italy, young athletes have been screened before participating in competitive sports. We… Expand
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Highly Cited
1995
Highly Cited
1995
BACKGROUND Hypertrophic cardiomyopathy (HCM) is a genetically transmitted disease and an important cause of morbidity and sudden… Expand
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Highly Cited
1994
Highly Cited
1994
  • M. B. Burch
  • Archives of disease in childhood
  • 1994
  • Corpus ID: 286185
Traditionally, the diagnosis of hypertrophic cardiomyopathy has been based on the presence of unexplained ventricular hypertrophy… Expand
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Highly Cited
1990
Highly Cited
1990
A point mutation in exon 13 of the beta cardiac myosin heavy chain (MHC) gene is present in all individuals affected with… Expand
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