Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1990 1
2007 1
2008 1
2010 1
2017 1
2020 1
2021 1
2023 0

Text availability

Article attribute

Article type

Publication date

Search Results

6 results

Results by year

Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
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.
Pathological features include loss of myocytes and fibrofatty replacement of right ventricular myocardium; biventricular involvement is often observed. It is a cell-to-cell junction cardiomyopathy, typically caused by genetically determined abnormalities of cardiac …
Pathological features include loss of myocytes and fibrofatty replacement of right ventricular myocardium; biventricular invol …
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria.
Marcus FI, McKenna WJ, Sherrill D, Basso C, Bauce B, Bluemke DA, Calkins H, Corrado D, Cox MG, Daubert JP, Fontaine G, Gear K, Hauer R, Nava A, Picard MH, Protonotarios N, Saffitz JE, Sanborn DM, Steinberg JS, Tandri H, Thiene G, Towbin JA, Tsatsopoulou A, Wichter T, Zareba W. Marcus FI, et al. Eur Heart J. 2010 Apr;31(7):806-14. doi: 10.1093/eurheartj/ehq025. Epub 2010 Feb 19. Eur Heart J. 2010. PMID: 20172912 Free PMC article.
BACKGROUND: In 1994, an International Task Force proposed criteria for the clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) that facilitated recognition and interpretation of the frequently nonspecific clinical f …
BACKGROUND: In 1994, an International Task Force proposed criteria for the clinical diagnosis of arrhythmogenic right ventr …
Arrhythmogenic cardiomyopathy: An in-depth look at molecular mechanisms and clinical correlates.
Costa S, Cerrone M, Saguner AM, Brunckhorst C, Delmar M, Duru F. Costa S, et al. Trends Cardiovasc Med. 2021 Oct;31(7):395-402. doi: 10.1016/j.tcm.2020.07.006. Epub 2020 Jul 29. Trends Cardiovasc Med. 2021. PMID: 32738304 Free article. Review.
Arrhythmogenic cardiomyopathy (ACM) is a familial disease, with approximately 60% of patients displaying a pathogenic variant. ...In turn, this may result in failure to mechanically hold together the cardiomyocytes, fibrofatty myocardial replacement, cardiac conduct …
Arrhythmogenic cardiomyopathy (ACM) is a familial disease, with approximately 60% of patients displaying a pathogenic variant. …
Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Sen-Chowdhry S, Syrris P, McKenna WJ. Sen-Chowdhry S, et al. J Am Coll Cardiol. 2007 Nov 6;50(19):1813-21. doi: 10.1016/j.jacc.2007.08.008. Epub 2007 Oct 24. J Am Coll Cardiol. 2007. PMID: 17980246 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a recognized cause of sudden cardiac death, which may be prevented by timely detection and intervention. ...A role for genetic analysis in prognostication is more tenuous at present, but increasing ide …
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a recognized cause of sudden cardiac death, which may be prev …
Genetic evaluation of familial cardiomyopathy.
Judge DP, Johnson NM. Judge DP, et al. J Cardiovasc Transl Res. 2008 Jun;1(2):144-54. doi: 10.1007/s12265-008-9025-1. Epub 2008 Apr 22. J Cardiovasc Transl Res. 2008. PMID: 20559909 Review.
Hereditary forms of hypertrophic, dilated, restrictive, and right ventricular cardiomyopathies are frequently seen. Patterns of inheritance include autosomal dominant, autosomal recessive, X-linked, and matrilinear. Recognition of the mode of inheritance facilitates …
Hereditary forms of hypertrophic, dilated, restrictive, and right ventricular cardiomyopathies are frequently seen. Patterns o …
[Congenital and acquired right ventricular dysplasia].
Fontaine G, Fontaliran F, Lascault G, Frank R, Tonet J, Chomette G, Grosgogeat Y. Fontaine G, et al. Arch Mal Coeur Vaiss. 1990 Jun;83(7):915-20. Arch Mal Coeur Vaiss. 1990. PMID: 2114851 Review. French.
Arrhythmogenic right ventricular dysplasia has been described as a developmental malformation occurring during foetal life. ...The authors suggest that in addition to the congenital form there may also be a possibility of acquiring arrhythmogenic …
Arrhythmogenic right ventricular dysplasia has been described as a developmental malformation occurring during f …