"Cardiomyopathy, Dilated" 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.
A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein.
Descriptor ID |
D002311
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MeSH Number(s) |
C14.280.195.160 C14.280.238.070
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Concept/Terms |
Cardiomyopathy, Dilated- Cardiomyopathy, Dilated
- Cardiomyopathies, Dilated
- Dilated Cardiomyopathies
- Dilated Cardiomyopathy
Cardiomyopathy, Familial Idiopathic- Cardiomyopathy, Familial Idiopathic
- Cardiomyopathies, Familial Idiopathic
- Familial Idiopathic Cardiomyopathies
- Familial Idiopathic Cardiomyopathy
- Idiopathic Cardiomyopathies, Familial
- Idiopathic Cardiomyopathy, Familial
- Cardiomyopathy, Congestive
- Cardiomyopathies, Congestive
- Congestive Cardiomyopathies
- Cardiomyopathy, Dilated, with Conduction Deffect1
- Cardiomyopathy, Dilated, CMD1A
- Dilated cardiomyopathy 1A
- 1As, Dilated cardiomyopathy
- Dilated cardiomyopathy 1As
- cardiomyopathy 1A, Dilated
- cardiomyopathy 1As, Dilated
- Cardiomyopathy, Dilated, Autosomal Recessive
- Cardiomyopathy, Dilated, 1a
- Cardiomyopathy, Dilated, With Conduction Defect 1
- Cardiomyopathy, Idiopathic Dilated
- Cardiomyopathies, Idiopathic Dilated
- Dilated Cardiomyopathies, Idiopathic
- Dilated Cardiomyopathy, Idiopathic
- Idiopathic Dilated Cardiomyopathies
- Idiopathic Dilated Cardiomyopathy
- Congestive Cardiomyopathy
- Cardiomyopathy, Dilated, LMNA
|
Below are MeSH descriptors whose meaning is more general than "Cardiomyopathy, Dilated".
Below are MeSH descriptors whose meaning is more specific than "Cardiomyopathy, Dilated".
This graph shows the total number of publications written about "Cardiomyopathy, Dilated" by people in this website by year, and whether "Cardiomyopathy, Dilated" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
---|
1999 | 0 | 1 | 1 |
2009 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2016 | 3 | 0 | 3 |
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Below are the most recent publications written about "Cardiomyopathy, Dilated" by people in Profiles.
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Upregulated Angiogenesis Is Incompetent to Rescue Dilated Cardiomyopathy Phenotype in Mice. Cells. 2021 03 31; 10(4).
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FTY720 (Gilenya) treatment prevents spontaneous autoimmune myocarditis and dilated cardiomyopathy in transgenic HLA-DQ8-BALB/c mice. Cardiovasc Pathol. 2016 Sep-Oct; 25(5):353-61.
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Ixmyelocel-T for patients with ischaemic heart failure: a prospective randomised double-blind trial. Lancet. 2016 Jun 11; 387(10036):2412-21.
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The ixCELL-DCM Trial: Rationale and Design. Cell Transplant. 2016; 25(9):1689-1699.
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Role of RyR2 phosphorylation at S2814 during heart failure progression. Circ Res. 2012 May 25; 110(11):1474-83.
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Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. Am J Hum Genet. 2011 Mar 11; 88(3):273-82.
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Ryanodine receptor Ca2+ sensitivity and excitation-contraction coupling in muscular dystrophy and heart failure: similar and yet different. Am J Physiol Heart Circ Physiol. 2009 Dec; 297(6):H1965-6.
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Akt regulates L-type Ca2+ channel activity by modulating Cavalpha1 protein stability. J Cell Biol. 2009 Mar 23; 184(6):923-33.
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Connexin 43 downregulation and dephosphorylation in nonischemic heart failure is associated with enhanced colocalized protein phosphatase type 2A. Circ Res. 2005 Jan 07; 96(1):54-63.
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Survival after myocardial revascularization for ischemic cardiomyopathy: a prospective ten-year follow-up study. J Thorac Cardiovasc Surg. 2003 Nov; 126(5):1320-7.