 Cardiomyopathy, Dilated
"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
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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, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1991 | 5 | 2 | 7 | | 1992 | 4 | 3 | 7 | | 1993 | 2 | 2 | 4 | | 1994 | 6 | 0 | 6 | | 1995 | 6 | 0 | 6 | | 1996 | 4 | 0 | 4 | | 1997 | 5 | 0 | 5 | | 1998 | 2 | 0 | 2 | | 1999 | 7 | 4 | 11 | | 2000 | 2 | 1 | 3 | | 2001 | 4 | 0 | 4 | | 2002 | 5 | 0 | 5 | | 2003 | 3 | 0 | 3 | | 2004 | 4 | 1 | 5 | | 2005 | 4 | 3 | 7 | | 2006 | 1 | 2 | 3 | | 2007 | 4 | 1 | 5 | | 2008 | 4 | 1 | 5 | | 2009 | 5 | 0 | 5 | | 2010 | 2 | 0 | 2 | | 2011 | 4 | 2 | 6 | | 2012 | 7 | 2 | 9 | | 2013 | 5 | 0 | 5 | | 2014 | 5 | 2 | 7 | | 2015 | 7 | 3 | 10 | | 2016 | 7 | 0 | 7 | | 2017 | 7 | 2 | 9 | | 2018 | 8 | 2 | 10 | | 2019 | 6 | 1 | 7 | | 2020 | 4 | 0 | 4 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cardiomyopathy, Dilated" by people in Profiles.
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Chen SN, Mestroni L, Taylor MRG. Genetics of dilated cardiomyopathy. Curr Opin Cardiol. 2021 05 01; 36(3):288-294.
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Eldemire R, Taylor MRG, Mestroni L. Understanding the role of titin in dilated cardiomyopathy. Int J Cardiol. 2020 10 01; 316:186-187.
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Merlo M, Cannatà A, Pio Loco C, Stolfo D, Barbati G, Artico J, Gentile P, De Paris V, Ramani F, Zecchin M, Gigli M, Pinamonti B, Korcova R, Di Lenarda A, Giacca M, Mestroni L, Camici PG, Sinagra G. Contemporary survival trends and aetiological characterization in non-ischaemic dilated cardiomyopathy. Eur J Heart Fail. 2020 07; 22(7):1111-1121.
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Finocchiaro G, Merlo M, Sheikh N, De Angelis G, Papadakis M, Olivotto I, Rapezzi C, Carr-White G, Sharma S, Mestroni L, Sinagra G. The electrocardiogram in the diagnosis and management of patients with dilated cardiomyopathy. Eur J Heart Fail. 2020 07; 22(7):1097-1107.
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Haywood ME, Cocciolo A, Porter KF, Dobrinskikh E, Slavov D, Graw SL, Reece TB, Ambardekar AV, Bristow MR, Mestroni L, Taylor MRG. Transcriptome signature of ventricular arrhythmia in dilated cardiomyopathy reveals increased fibrosis and activated TP53. J Mol Cell Cardiol. 2020 02; 139:124-134.
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Chen SN, Sbaizero O, Taylor MRG, Mestroni L. Lamin A/C Cardiomyopathy: Implications for Treatment. Curr Cardiol Rep. 2019 11 26; 21(12):160.
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Nakano SJ, Miyamoto SD, Price JF, Rossano JW, Cabrera AG. Pediatric Heart Failure: An Evolving Public Health Concern. J Pediatr. 2020 03; 218:217-221.
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Nakano SJ, Walker JS, Walker LA, Li X, Du Y, Miyamoto SD, Sucharov CC, Garcia AM, Mitchell MB, Ambardekar AV, Stauffer BL. Increased myocyte calcium sensitivity in end-stage pediatric dilated cardiomyopathy. Am J Physiol Heart Circ Physiol. 2019 12 01; 317(6):H1221-H1230.
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Gigli M, Merlo M, Graw SL, Barbati G, Rowland TJ, Slavov DB, Stolfo D, Haywood ME, Dal Ferro M, Altinier A, Ramani F, Brun F, Cocciolo A, Puggia I, Morea G, McKenna WJ, La Rosa FG, Taylor MRG, Sinagra G, Mestroni L. Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy. J Am Coll Cardiol. 2019 09 17; 74(11):1480-1490.
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Peter AK, Rossi AC, Buvoli M, Ozeroff CD, Crocini C, Perry AR, Buvoli AE, Lee LA, Leinwand LA. Expression of Normally Repressed Myosin Heavy Chain 7b in the Mammalian Heart Induces Dilated Cardiomyopathy. J Am Heart Assoc. 2019 08 06; 8(15):e013318.
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