Cardiomyopathies

"Cardiomyopathies" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS).

Descriptor ID	D009202
MeSH Number(s)	C14.280.238
Concept/Terms	Cardiomyopathies Cardiomyopathies Cardiomyopathy Myocardial Diseases Disease, Myocardial Diseases, Myocardial Myocardial Disease Myocardiopathies Myocardiopathy Cardiomyopathies, Secondary Cardiomyopathies, Secondary Cardiomyopathy, Secondary Secondary Cardiomyopathies Secondary Cardiomyopathy Secondary Myocardial Diseases Disease, Secondary Myocardial Diseases, Secondary Myocardial Myocardial Disease, Secondary Secondary Myocardial Disease Myocardial Diseases, Secondary Cardiomyopathies, Primary Cardiomyopathies, Primary Cardiomyopathy, Primary Primary Cardiomyopathies Primary Cardiomyopathy Primary Myocardial Diseases Myocardial Diseases, Primary Disease, Primary Myocardial Diseases, Primary Myocardial Myocardial Disease, Primary Primary Myocardial Disease

Below are MeSH descriptors whose meaning is more general than "Cardiomyopathies".

Diseases [C]
Cardiovascular Diseases [C14]
Heart Diseases [C14.280]
Cardiomyopathies [C14.280.238]

Below are MeSH descriptors whose meaning is more specific than "Cardiomyopathies".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Cardiomyopathies" by people in this website by year, and whether "Cardiomyopathies" was a major or minor topic of these publications.

Bar chart showing 100 publications over 24 distinct years, with a maximum of 8 publications in 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1997	1	0	1
1998	1	0	1
2000	0	2	2
2002	0	1	1
2003	1	3	4
2004	2	1	3
2005	3	1	4
2006	0	3	3
2007	5	1	6
2008	4	2	6
2009	1	2	3
2010	4	1	5
2011	4	2	6
2012	4	1	5
2013	1	1	2
2014	6	0	6
2015	7	0	7
2016	4	0	4
2017	5	1	6
2018	3	0	3
2019	1	2	3
2020	6	1	7
2021	7	1	8
2022	4	0	4

Below are the most recent publications written about "Cardiomyopathies" by people in Profiles.

Whellan D, McCarey MM, Chen H, Nelson MB, Pastva AM, Duncan P, Mentz RJ, Kitzman DW, Reeves G, Reed SD. Quality of Life Trajectory and Its Mediators in Older Patients With Acute Decompensated Heart Failure Receiving a Multi-Domain Rehabilitation Intervention: Results From the Rehabilitation Therapy in Older Acute Heart Failure Patients Trial. Circ Heart Fail. 2022 12; 15(12):e009695.

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Berberian JG. Hereditary Syndromes of Sudden Cardiac Death. Emerg Med Clin North Am. 2022 Nov; 40(4):651-662.

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Wollenhaupt J, Frisch J, Harlacher E, Wong DWL, Jin H, Schulte C, Vondenhoff S, Moellmann J, Klinkhammer BM, Zhang L, Baleanu-Curaj A, Liehn EA, Speer T, Kazakov A, Werner C, van der Vorst EPC, Selejan SR, Hohl M, B?hm M, Kramann R, Biessen EAL, Lehrke M, Marx N, Jankowski J, Maack C, Boor P, Prates Roma L, Noels H. Pro-oxidative priming but maintained cardiac function in a broad spectrum of murine models of chronic kidney disease. Redox Biol. 2022 10; 56:102459.

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Olanipekun T, Abe T, Effoe V, Egbuche O, Mather P, Echols M, Adedinsewo D. Racial and Ethnic Disparities in the Trends and Outcomes of Cardiogenic Shock Complicating Peripartum Cardiomyopathy. JAMA Netw Open. 2022 Jul 01; 5(7):e2220937.

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Krebs J, Mansi T, Delingette H, Lou B, Lima JAC, Tao S, Ciuffo LA, Norgard S, Butcher B, Lee WH, Chamera E, Dickfeld TM, Stillabower M, Marine JE, Weiss RG, Tomaselli GF, Halperin H, Wu KC, Ashikaga H. CinE caRdiac magneTic resonAnce to predIct veNTricular arrhYthmia (CERTAINTY). Sci Rep. 2021 11 22; 11(1):22683.

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Sheybani A, Crum K, Raucci FJ, Burnette WB, Markham LW, Soslow JH. Duchenne muscular dystrophy patients: troponin leak in asymptomatic and implications for drug toxicity studies. Pediatr Res. 2022 12; 92(6):1613-1620.

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Wu P, Jordan KP, Chew-Graham CA, Mohamed MO, Barac A, Lundberg GP, Chappell LC, Michos ED, Maas AHEM, Mamas MA. In-Hospital Complications in Pregnant Women With Current or Historical Cancer Diagnoses. Mayo Clin Proc. 2021 11; 96(11):2779-2792.

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D'Agostino I, Tacconelli S, Bruno A, Contursi A, Mucci L, Hu X, Xie Y, Chakraborty R, Jain K, Sacco A, Zucchelli M, Landolfi R, Dovizio M, Falcone L, Ballerini P, Hwa J, Patrignani P. Low-dose Aspirin prevents hypertension and cardiac fibrosis when thromboxane A2 is unrestrained. Pharmacol Res. 2021 08; 170:105744.

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Husser D, Pellissier V, Hohenstein S, Ueberham L, K?nig S, Hindricks G, Meier-Hellmann A, Kuhlen R, Bollmann A. Hospital care of patients with inherited cardiomyopathies in Germany during the Covid-19 pandemic insights from the German-wide Helios hospital network. Am J Med Genet A. 2021 07; 185(7):2278-2282.

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Greenberg MJ, Tardiff JC. Complexity in genetic cardiomyopathies and new approaches for mechanism-based precision medicine. J Gen Physiol. 2021 03 01; 153(3).

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