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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 123
2022 110
2023 63

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1,726 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.
Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can cause exertional dyspnea, presyncope, atypical chest pain, heart failure, and sudden cardiac death. ...Family physicians should be alert for acquired variants of cardiomyopathy …
Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can cause exertional dyspnea, presyncope, atypical c …
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 …
The Diagnosis and Evaluation of Dilated Cardiomyopathy.
Japp AG, Gulati A, Cook SA, Cowie MR, Prasad SK. Japp AG, et al. J Am Coll Cardiol. 2016 Jun 28;67(25):2996-3010. doi: 10.1016/j.jacc.2016.03.590. J Am Coll Cardiol. 2016. PMID: 27339497 Free article. Review.
Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and environmental insults. A rigorous work-up can exclude alternative causes of left ventricular (LV) dilation and dysfunction, identify etiologies that may respon …
Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and environmental insul …
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. ...
Cardiac amyloidosis (CA) is an infiltrative and restrictive cardiomyopathy that leads to heart failure, reduced quality of life, and …
RNA-targeting and gene editing therapies for transthyretin amyloidosis.
Aimo A, Castiglione V, Rapezzi C, Franzini M, Panichella G, Vergaro G, Gillmore J, Fontana M, Passino C, Emdin M. Aimo A, et al. Nat Rev Cardiol. 2022 Oct;19(10):655-667. doi: 10.1038/s41569-022-00683-z. Epub 2022 Mar 23. Nat Rev Cardiol. 2022. PMID: 35322226 Review.
The siRNA patisiran and the ASO inotersen have been approved for the treatment of patients with ATTR variant polyneuropathy, regardless of the presence and severity of ATTR cardiomyopathy. Preliminary data show that therapy with patisiran improves the cardiac phenotype rat …
The siRNA patisiran and the ASO inotersen have been approved for the treatment of patients with ATTR variant polyneuropathy, regardless of t …
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 …
Familial Dilated Cardiomyopathy.
Peters S, Johnson R, Birch S, Zentner D, Hershberger RE, Fatkin D. Peters S, et al. Heart Lung Circ. 2020 Apr;29(4):566-574. doi: 10.1016/j.hlc.2019.11.018. Epub 2019 Dec 17. Heart Lung Circ. 2020. PMID: 31974027 Review.
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (DCM), facilitating genetic testing and clinical applications. ...Although there are several examples of successful genotype-based therapy, optimal strategies for implementat …
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (DCM), facilitating genetic testin …
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy.
Marian AJ, Braunwald E. Marian AJ, et al. Circ Res. 2017 Sep 15;121(7):749-770. doi: 10.1161/CIRCRESAHA.117.311059. Circ Res. 2017. PMID: 28912181 Free PMC article. Review.
Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left ventricular hypertrophy unexplained by secondary causes and a nondilated left ventricle with preserved or increased ejection fraction. ...MYH7 and MYBPC3, encoding beta-myosin heavy chain …
Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left ventricular hypertrophy unexplained by secondar …
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 …
1,726 results