Cardiomyopathy, Hypertrophic, Familial
"Cardiomyopathy, Hypertrophic, Familial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.
MeSH Number(s)
C14.280.238.100.500
C16.320.160
Concept/Terms
Cardiomyopathy, Hypertrophic, Familial- Cardiomyopathy, Hypertrophic, Familial
- Ventricular Hypertrophy, Familial
- Familial Ventricular Hypertrophies
- Familial Ventricular Hypertrophy
- Hypertrophy, Familial Ventricular
- Ventricular Hypertrophies, Familial
- Familial Hypertrophic Cardiomyopathy
- Hereditary Ventricular Hypertrophy
- Hereditary Ventricular Hypertrophies
- Hypertrophies, Hereditary Ventricular
- Hypertrophy, Hereditary Ventricular
- Ventricular Hypertrophies, Hereditary
- Asymmetric Septal Hypertrophy, Familial
- Cardiomyopathy, Familial Hypertrophic
- Cardiomyopathies, Familial Hypertrophic
- Familial Hypertrophic Cardiomyopathies
- Hypertrophic Cardiomyopathies, Familial
- Hypertrophic Cardiomyopathy, Familial
Below are MeSH descriptors whose meaning is more general than "Cardiomyopathy, Hypertrophic, Familial".
Below are MeSH descriptors whose meaning is more specific than "Cardiomyopathy, Hypertrophic, Familial".
This graph shows the total number of publications written about "Cardiomyopathy, Hypertrophic, Familial" by people in Harvard Catalyst Profiles by year, and whether "Cardiomyopathy, Hypertrophic, Familial" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 1 | 2 |
| 2002 | 4 | 2 | 6 |
| 2004 | 1 | 1 | 2 |
| 2005 | 0 | 1 | 1 |
| 2006 | 2 | 0 | 2 |
| 2007 | 1 | 0 | 1 |
| 2008 | 1 | 2 | 3 |
| 2009 | 4 | 0 | 4 |
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 0 | 1 |
| 2012 | 2 | 1 | 3 |
| 2013 | 1 | 1 | 2 |
| 2014 | 1 | 0 | 1 |
| 2016 | 3 | 0 | 3 |
| 2017 | 3 | 0 | 3 |
| 2018 | 2 | 0 | 2 |
| 2019 | 0 | 1 | 1 |
Below are the most recent publications written about "Cardiomyopathy, Hypertrophic, Familial" by people in Profiles.
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Case 16-2019: A 53-Year-Old Man with Cough and Eosinophilia. N Engl J Med. 2019 May 23; 380(21):2052-2059.
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Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes. Circ Genom Precis Med. 2019 02; 12(2):e002460.
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Significance of Pulmonary Hypertension in Hypertrophic Cardiomyopathy. Curr Probl Cardiol. 2020 Jun; 45(6):100398.
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Telomere shortening is a hallmark of genetic cardiomyopathies. Proc Natl Acad Sci U S A. 2018 09 11; 115(37):9276-9281.
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Cardiovascular homeostasis dependence on MICU2, a regulatory subunit of the mitochondrial calcium uniporter. Proc Natl Acad Sci U S A. 2017 10 24; 114(43):E9096-E9104.
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Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (ß-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy. Circ Cardiovasc Imaging. 2017 Feb; 10(2).
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Early remodeling of repolarizing K+ currents in the aMHC403/+ mouse model of familial hypertrophic cardiomyopathy. J Mol Cell Cardiol. 2017 02; 103:93-101.
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A Tension-Based Model Distinguishes Hypertrophic versus Dilated Cardiomyopathy. Cell. 2016 May 19; 165(5):1147-1159.
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Disheartening Disparities. N Engl J Med. 2016 Mar 10; 374(10):909-11.
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Hypertrophic Cardiomyopathy from A to Z: Genetics, Pathophysiology, Imaging, and Management. Radiographics. 2016 Mar-Apr; 36(2):335-54.