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 |
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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 | 3 | 2 | 5 | 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 | 4 | 1 | 5 | 2013 | 5 | 0 | 5 | 2014 | 5 | 2 | 7 | 2015 | 7 | 2 | 9 | 2016 | 6 | 0 | 6 | 2017 | 6 | 1 | 7 | 2018 | 8 | 2 | 10 | 2019 | 7 | 1 | 8 | 2020 | 4 | 1 | 5 | 2021 | 6 | 1 | 7 | 2022 | 6 | 0 | 6 |
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Below are the most recent publications written about "Cardiomyopathy, Dilated" by people in Profiles.
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Murphey K, George PE, Pencheva B, Porter CC, Wechsler SB, Gambello MJ, Li H. Acute myeloid leukemia and dilated cardiomyopathy in a pediatric patient with D-2-hydroxyglutaric aciduria type I. Am J Med Genet A. 2022 09; 188(9):2707-2711.
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Aly DM, Nguyen M, Auerbach S, Rausch C, Landeck B, DiMaria MV. Pressure-Strain Loops, a Novel Non-invasive Approach for Assessment of Children with Cardiomyopathy. Pediatr Cardiol. 2022 Dec; 43(8):1704-1715.
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Cannatà A, Merlo M, Dal Ferro M, Barbati G, Manca P, Paldino A, Graw S, Gigli M, Stolfo D, Johnson R, Roy D, Tharratt K, Bromage DI, Jirikowic J, Abbate A, Goodwin A, Rao K, Marawan A, Carr-White G, Robert L, Parikh V, Ashley E, McDonagh T, Lakdawala NK, Fatkin D, Taylor MRG, Mestroni L, Sinagra G. Association of Titin Variations With Late-Onset Dilated Cardiomyopathy. JAMA Cardiol. 2022 04 01; 7(4):371-377.
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Lehman SJ, Crocini C, Leinwand LA. Targeting the sarcomere in inherited cardiomyopathies. Nat Rev Cardiol. 2022 06; 19(6):353-363.
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Purmah Y, Cornhill A, Lei LY, Dykstra S, Mikami Y, Satriano A, Labib D, Flewitt J, Rivest S, Sandonato R, Seib M, Howarth AG, Lydell CP, Heydari B, Merchant N, Bristow M, Kolman L, Fine NM, White JA. Mid-wall striae fibrosis predicts heart failure admission, composite heart failure events, and life-threatening arrhythmias in dilated cardiomyopathy. Sci Rep. 2022 02 02; 12(1):1739.
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Ware SM, Bhatnagar S, Dexheimer PJ, Wilkinson JD, Sridhar A, Fan X, Shen Y, Tariq M, Schubert JA, Colan SD, Shi L, Canter CE, Hsu DT, Bansal N, Webber SA, Everitt MD, Kantor PF, Rossano JW, Pahl E, Rusconi P, Lee TM, Towbin JA, Lal AK, Chung WK, Miller EM, Aronow B, Martin LJ, Lipshultz SE. The genetic architecture of pediatric cardiomyopathy. Am J Hum Genet. 2022 02 03; 109(2):282-298.
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Gao S, Mumme-Monheit A, Chen SN, Spector EB, Slavov D, Baralle FE, Bristow MR, Mestroni L, Taylor MRG. An LMNA synonymous variant associated with severe dilated cardiomyopathy: Case report. Am J Med Genet A. 2022 02; 188(2):600-605.
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Jeffrey DA, Pires Da Silva J, Garcia AM, Jiang X, Karimpour-Fard A, Toni LS, Lanzicher T, Peña B, Miyano CA, Nunley K, Korst A, Sbaizero O, Taylor MR, Miyamoto SD, Stauffer BL, Sucharov CC. Serum circulating proteins from pediatric patients with dilated cardiomyopathy cause pathologic remodeling and cardiomyocyte stiffness. JCI Insight. 2021 10 08; 6(19).
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Gropler MRF, Lipshultz SE, Wilkinson JD, Towbin JA, Colan SD, Canter CE, Lavine KJ, Simpson KE. Pediatric and adult dilated cardiomyopathy are distinguished by distinct biomarker profiles. Pediatr Res. 2022 07; 92(1):206-215.
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Manca P, Cannatà A, Nuzzi V, Bromage DI, Varrà GG, Rossi M, Dal Ferro M, Paldino A, Gigli M, Barbati G, Ramani F, Pinamonti B, Stolfo D, Porcu M, Mestroni L, Merlo M, Sinagra G. Prevalence and Evolution of Right Ventricular Dysfunction Among Different Genetic Backgrounds in Dilated Cardiomyopathy. Can J Cardiol. 2021 11; 37(11):1743-1750.
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