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

Year Number of Results
1989 1
1990 1
1991 1
1995 1
1996 2
1997 2
1998 4
2000 2
2001 1
2002 4
2003 2
2004 4
2005 8
2006 4
2007 2
2008 8
2009 5
2010 4
2011 4
2012 2
2013 4
2014 11
2015 7
2016 5
2017 13
2018 5
2019 5
2020 5
2021 1
2022 2
2023 5
2024 2

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116 results

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Page 1
Management of arrhythmogenic right ventricular cardiomyopathy.
Al-Aidarous S, Protonotarios A, Elliott PM, Lambiase PD. Al-Aidarous S, et al. Heart. 2024 Jan 10;110(3):156-162. doi: 10.1136/heartjnl-2023-322612. Heart. 2024. PMID: 37433658 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a disease characterised by fibrofatty replacement of the ventricular myocardium due to specific mutations, leading to ventricular arrhythmias and sudden cardiac death. ...Emerging evidenc
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a disease characterised by fibrofatty replacement of the v
Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update.
Azaouagh A, Churzidse S, Konorza T, Erbel R. Azaouagh A, et al. Clin Res Cardiol. 2011 May;100(5):383-94. doi: 10.1007/s00392-011-0295-2. Epub 2011 Mar 1. Clin Res Cardiol. 2011. PMID: 21360243 Review.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a predominantly genetically determined and heritable form of cardiomyopathy that is characterized pathologically by the replacement of myocytes by adipose and fibrous tissue and lead
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a predominantly genetically determined and
Arrhythmogenic right ventricular dysplasia.
Calkins H. Calkins H. Curr Probl Cardiol. 2013 Mar;38(3):103-23. doi: 10.1016/j.cpcardiol.2012.12.002. Curr Probl Cardiol. 2013. PMID: 23453020 Review.
Arrhythmogenic right ventricular dysplasia (ARVD) is an inherited cardiomyopathy and is also called ARVD/C. In most cases, ARVD is inherited in an autosomal-dominant pattern and clinically is characterized by ventricular arrhythmias with an incr
Arrhythmogenic right ventricular dysplasia (ARVD) is an inherited cardiomyopathy and is also called ARVD/C. In m
Multimodality Imaging in Arrhythmogenic Right Ventricular Cardiomyopathy.
Malik N, Mukherjee M, Wu KC, Zimmerman SL, Zhan J, Calkins H, James CA, Gilotra NA, Sheikh FH, Tandri H, Kutty S, Hays AG. Malik N, et al. Circ Cardiovasc Imaging. 2022 Feb;15(2):e013725. doi: 10.1161/CIRCIMAGING.121.013725. Epub 2022 Feb 11. Circ Cardiovasc Imaging. 2022. PMID: 35147040 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare, heritable myocardial disease associated with the development of ventricular arrhythmias, heart failure, and sudden cardiac death in early adulthood. ...Diagnostic criteria established by
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare, heritable myocardial disease associated with the deve
Considerations for specific cardiomyopathies during pregnancy.
Abrams M, Magun E, DeFilippis EM. Abrams M, et al. Curr Opin Cardiol. 2023 May 1;38(3):233-240. doi: 10.1097/HCO.0000000000001033. Epub 2023 Mar 1. Curr Opin Cardiol. 2023. PMID: 37016994 Review.
Herein, we review and synthesize recent studies focusing on preconception risk and counseling, pharmacologic management, and maternal outcomes in various cardiomyopathies during pregnancy including: dilated cardiomyopathy, hypertrophic cardiomyopathy, arrhythmogenic rig
Herein, we review and synthesize recent studies focusing on preconception risk and counseling, pharmacologic management, and maternal outcom …
Myocardial voltage ratio in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Müssigbrodt A, Bertagnolli L, Efimova E, Kosiuk J, Dinov B, Bode K, Kircher S, Dagres N, Döring M, Richter S, Sommer P, Husser D, Bollmann A, Hindricks G, Arya A. Müssigbrodt A, et al. Herzschrittmacherther Elektrophysiol. 2017 Jun;28(2):219-224. doi: 10.1007/s00399-017-0508-0. Epub 2017 May 23. Herzschrittmacherther Elektrophysiol. 2017. PMID: 28536891 Review. English.
AIMS: This study aimed to analyze the influence of scar distribution between the endocardium and the epicardium in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). METHODS: Electroanatomical mapping data were derived fr …
AIMS: This study aimed to analyze the influence of scar distribution between the endocardium and the epicardium in patients with arrhythm
Arrhythmogenic Cardiomyopathy and Athletes: A Dangerous Relationship.
de la Guía-Galipienso F, Ugedo-Alzaga K, Grazioli G, Quesada-Ocete FJ, Feliu-Rey E, Perez MV, Quesada-Dorador A, Sanchis-Gomar F. de la Guía-Galipienso F, et al. Curr Probl Cardiol. 2023 Sep;48(9):101799. doi: 10.1016/j.cpcardiol.2023.101799. Epub 2023 May 11. Curr Probl Cardiol. 2023. PMID: 37172878 Review.
Arrhythmogenic cardiomyopathy (ACM) is a disease characterized by a progressive replacement of myocardium by fibro-adipose material, predisposing to ventricular arrhythmias (VA) and sudden cardiac death (SCD). ...Estimating the incidence of SCD caused by ACM in athl
Arrhythmogenic cardiomyopathy (ACM) is a disease characterized by a progressive replacement of myocardium by fibro-adipose material,
Genetic Risk Stratification in Arrhythmogenic Left Ventricular Cardiomyopathy.
Desai YB, Parikh VN. Desai YB, et al. Card Electrophysiol Clin. 2023 Sep;15(3):391-399. doi: 10.1016/j.ccep.2023.04.005. Epub 2023 Jun 20. Card Electrophysiol Clin. 2023. PMID: 37558308 Review.
Arrhythmogenic left ventricular cardiomyopathy is characterized by early malignant ventricular arrhythmia associated with varying degrees and times of onset of left ventricular dysfunction. ...Unlike traditional sudden cardiac death risk assessment in
Arrhythmogenic left ventricular cardiomyopathy is characterized by early malignant ventricular arrhythmia associated wi
Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy.
Calkins H, Corrado D, Marcus F. Calkins H, et al. Circulation. 2017 Nov 21;136(21):2068-2082. doi: 10.1161/CIRCULATIONAHA.117.030792. Circulation. 2017. PMID: 29158215 Free PMC article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized by ventricular arrhythmias and an increased risk of sudden cardiac death. Although structural abnormalities of the right ventricle predominate, i
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized by ventricular
Epicardial Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy.
Assis FR, Tandri H. Assis FR, et al. Card Electrophysiol Clin. 2020 Sep;12(3):329-343. doi: 10.1016/j.ccep.2020.05.005. Epub 2020 Jul 8. Card Electrophysiol Clin. 2020. PMID: 32771187 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease characterized by progressive fibrofatty replacement of the myocardium, right ventricular enlargement, and malignant ventricular arrhythmias. Ve
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease characterized by progressiv
116 results