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1964
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 1
1970 1
1971 2
1975 1
1976 2
1977 1
1980 3
1982 1
1983 1
1984 2
1985 4
1987 4
1988 4
1989 8
1990 8
1991 9
1992 11
1993 19
1994 24
1995 24
1996 19
1997 20
1998 28
1999 24
2000 38
2001 40
2002 55
2003 49
2004 52
2005 46
2006 46
2007 39
2008 53
2009 60
2010 77
2011 76
2012 72
2013 76
2014 69
2015 95
2016 71
2017 103
2018 90
2019 96
2020 97
2021 125
2022 110
2023 108
2024 146
2025 5

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1,897 results

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Page 1
Cardiomyopathy: An Overview.
Brieler J, Breeden MA, Tucker J. Brieler J, et al. Am Fam Physician. 2017 Nov 15;96(10):640-646. Am Fam Physician. 2017. PMID: 29431384 Free article. Review.
Restrictive cardiomyopathy is much less common and often associated with systemic disease. Family physicians should be alert for acquired variants of cardiomyopathy, including peripartum and stress-induced cardiomyopathy, as well as rare variants, such …
Restrictive cardiomyopathy is much less common and often associated with systemic disease. Family physicians should be alert f …
Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review.
Ruberg FL, Grogan M, Hanna M, Kelly JW, Maurer MS. Ruberg FL, et al. J Am Coll Cardiol. 2019 Jun 11;73(22):2872-2891. doi: 10.1016/j.jacc.2019.04.003. J Am Coll Cardiol. 2019. PMID: 31171094 Free PMC article. Review.
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an under-recognized cause of heart failure (HF) in older adults, resulting from myocardial deposition of misfolded transthyretin (TTR) or pre-albumin. ...
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an under-recognized cause of heart failure (HF) in older adults, resulting from myo …
Familial Hypertrophic Cardiomyopathy: Diagnosis and Management.
Litt MJ, Ali A, Reza N. Litt MJ, et al. Vasc Health Risk Manag. 2023 Apr 6;19:211-221. doi: 10.2147/VHRM.S365001. eCollection 2023. Vasc Health Risk Manag. 2023. PMID: 37050929 Free PMC article. Review.
Hypertrophic cardiomyopathy (HCM) is widely recognized as one of the most common inheritable cardiac disorders. ...
Hypertrophic cardiomyopathy (HCM) is widely recognized as one of the most common inheritable cardiac disorders. ...
Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
Hershberger RE, Givertz MM, Ho CY, Judge DP, Kantor PF, McBride KL, Morales A, Taylor MRG, Vatta M, Ware SM. Hershberger RE, et al. J Card Fail. 2018 May;24(5):281-302. doi: 10.1016/j.cardfail.2018.03.004. Epub 2018 Mar 19. J Card Fail. 2018. PMID: 29567486 Free PMC article. Review.
The writing group, composed of cardiologists and genetics professionals with expertise in adult and pediatric cardiomyopathy, reflects the emergence and increased clinical activity devoted to cardiovascular genetic medicine. ...A systematic approach is recommended: always …
The writing group, composed of cardiologists and genetics professionals with expertise in adult and pediatric cardiomyopathy, reflect …
Arrhythmogenic Cardiomyopathy.
Corrado D, Basso C, Judge DP. Corrado D, et al. Circ Res. 2017 Sep 15;121(7):784-802. doi: 10.1161/CIRCRESAHA.117.309345. Circ Res. 2017. PMID: 28912183 Review.
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes. ...The diagnosis of arrhythmogenic cardiomyopathy does not rely on a single gold standard test but is achieved usi …
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young pati …
Neonatal dilated cardiomyopathy.
Soares P, Rocha G, Pissarra S, Soares H, Flôr-de-Lima F, Costa S, Moura C, Dória S, Guimarães H. Soares P, et al. Rev Port Cardiol. 2017 Mar;36(3):201-214. doi: 10.1016/j.repc.2016.10.007. Epub 2017 Feb 28. Rev Port Cardiol. 2017. PMID: 28256370 Free article. Review. English, Portuguese.
Dilated cardiomyopathy is the commonest cardiomyopathy in children, and the majority present before one year of age. ...Myocarditis is an important cause and is responsible for the majority of acquired cases. Inherited (familial) forms of dilated cardiomyo
Dilated cardiomyopathy is the commonest cardiomyopathy in children, and the majority present before one year of age. ...Myocar …
Epidemiology of the inherited cardiomyopathies.
McKenna WJ, Judge DP. McKenna WJ, et al. Nat Rev Cardiol. 2021 Jan;18(1):22-36. doi: 10.1038/s41569-020-0428-2. Epub 2020 Sep 7. Nat Rev Cardiol. 2021. PMID: 32895535 Review.
The global estimates for hypertrophic cardiomyopathy (1/500 individuals), dilated cardiomyopathy (1/250) and arrhythmogenic right ventricular cardiomyopathy (1/5,000) are probably conservative given that only individuals who fulfil diagnostic criteria would h …
The global estimates for hypertrophic cardiomyopathy (1/500 individuals), dilated cardiomyopathy (1/250) and arrhythmogenic ri …
Evolving concepts in dilated cardiomyopathy.
Merlo M, Cannatà A, Gobbo M, Stolfo D, Elliott PM, Sinagra G. Merlo M, et al. Eur J Heart Fail. 2018 Feb;20(2):228-239. doi: 10.1002/ejhf.1103. Epub 2017 Dec 22. Eur J Heart Fail. 2018. PMID: 29271570 Free article. Review.
Dilated cardiomyopathy (DCM) represents a particular aetiology of systolic heart failure that frequently has a genetic background and usually affects young patients with few co-morbidities. The prognosis of DCM has improved substantially during the last decades due to more …
Dilated cardiomyopathy (DCM) represents a particular aetiology of systolic heart failure that frequently has a genetic background and …
Cardiac Amyloidosis: Overlooked, Underappreciated, and Treatable.
Rubin J, Maurer MS. Rubin J, et al. Annu Rev Med. 2020 Jan 27;71:203-219. doi: 10.1146/annurev-med-052918-020140. Annu Rev Med. 2020. PMID: 31986086 Review.
Cardiac amyloidosis (CA) is an infiltrative and restrictive cardiomyopathy that leads to heart failure, reduced quality of life, and death. The disease has two main subtypes, transthyretin cardiac amyloidosis (ATTR-CA) and immunoglobulin light chain cardiac amyloidosis (AL …
Cardiac amyloidosis (CA) is an infiltrative and restrictive cardiomyopathy that leads to heart failure, reduced quality of life, and …
ATTR Epidemiology, Genetics, and Prognostic Factors.
Obi CA, Mostertz WC, Griffin JM, Judge DP. Obi CA, et al. Methodist Debakey Cardiovasc J. 2022 Mar 14;18(2):17-26. doi: 10.14797/mdcvj.1066. eCollection 2022. Methodist Debakey Cardiovasc J. 2022. PMID: 35414855 Free PMC article. Review.
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an underdiagnosed disease and an underestimated cause of both heart failure and conduction abnormalities. ...
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an underdiagnosed disease and an underestimated cause of both heart failure and con …
1,897 results