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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
1992 1
1993 2
1994 1
1995 3
1996 2
1997 4
1998 3
2000 6
2001 6
2002 4
2003 4
2004 7
2005 9
2006 6
2007 4
2008 11
2009 9
2010 4
2011 3
2012 7
2013 4
2014 13
2015 6
2016 10
2017 14
2018 10
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2020 2
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2022 7
2023 7
2024 2

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169 results

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Page 1
Arrhythmogenic Right Ventricular Cardiomyopathy.
Krahn AD, Wilde AAM, Calkins H, La Gerche A, Cadrin-Tourigny J, Roberts JD, Han HC. Krahn AD, et al. JACC Clin Electrophysiol. 2022 Apr;8(4):533-553. doi: 10.1016/j.jacep.2021.12.002. JACC Clin Electrophysiol. 2022. PMID: 35450611 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) encompasses a group of conditions characterized by right ventricular fibrofatty infiltration, with a predominant arrhythmic presentation. First described in the late 1970s and early 1980s, i
Arrhythmogenic right ventricular cardiomyopathy (ARVC) encompasses a group of conditions characterized by right
Arrhythmogenic Right Ventricular Cardiomyopathy.
Corrado D, Link MS, Calkins H. Corrado D, et al. N Engl J Med. 2017 Jan 5;376(1):61-72. doi: 10.1056/NEJMra1509267. N Engl J Med. 2017. PMID: 28052233 Review. No abstract available.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: an electrocardiogram-based review.
Nunes de Alencar Neto J, Baranchuk A, Bayés-Genís A, Bayés de Luna A. Nunes de Alencar Neto J, et al. Europace. 2018 Jun 1;20(FI1):f3-f12. doi: 10.1093/europace/eux202. Europace. 2018. PMID: 29272363 Review.
Arrhythmogenic right ventricular dysplasia or cardiomyopathy (ARVD/C) is a pathologic condition where the right ventricle is partially or totally replaced by fatty and fibrous tissue. ...More common ventricular arrhythmias and risk of sud
Arrhythmogenic right ventricular dysplasia or cardiomyopathy (ARVD/C) is a pathologic condition where the rig
Differential diagnosis of rSr' pattern in leads V1 -V2. Comprehensive review and proposed algorithm.
Baranchuk A, Enriquez A, García-Niebla J, Bayés-Genís A, Villuendas R, Bayés de Luna A. Baranchuk A, et al. Ann Noninvasive Electrocardiol. 2015 Jan;20(1):7-17. doi: 10.1111/anec.12241. Epub 2014 Dec 26. Ann Noninvasive Electrocardiol. 2015. PMID: 25546557 Free PMC article. Review.
We often face this finding in asymptomatic and otherwise healthy individuals and the causes may vary from benign nonpathological variants to severe or life-threatening heart diseases, such as Brugada syndrome or arrhythmogenic right ventricular dysplasia
We often face this finding in asymptomatic and otherwise healthy individuals and the causes may vary from benign nonpathological variants to …
Diagnostic and therapeutic strategies for arrhythmogenic right ventricular dysplasia/cardiomyopathy patient.
Wang W, James CA, Calkins H. Wang W, et al. Europace. 2019 Jan 1;21(1):9-21. doi: 10.1093/europace/euy063. Europace. 2019. PMID: 29688316 Free PMC article. Review.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a rare inherited heart muscle disease characterized by ventricular tachyarrhythmia, predominant right ventricular dysfunction, and sudden cardiac death. ...Exerc
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a rare inherited heart muscle disease char
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/cardiomyopathy.
Calkins H. Calkins H. Curr Opin Cardiol. 2006 Jan;21(1):55-63. doi: 10.1097/01.hco.0000198984.70884.4d. Curr Opin Cardiol. 2006. PMID: 16355031 Review.
PURPOSE OF REVIEW: Arrhythmogenic right-ventricular dysplasia is a rare inherited disease characterized by right-ventricular dysfunction and ventricular arrhythmias. ...This may explain why arrhythmogenic right-ven
PURPOSE OF REVIEW: Arrhythmogenic right-ventricular dysplasia is a rare inherited disease characterized by ri
[The 'Dangerous' ECG].
Flury G. Flury G. Praxis (Bern 1994). 2019 Jan;108(1):45-52. doi: 10.1024/1661-8157/a003155. Praxis (Bern 1994). 2019. PMID: 30621532 Review. German.
This review aims to draw the attention of physicians confronted with cardiac emergencies to some specific ECG pathomorphologies in acute coronary syndrome and pulmonary embolism, as well as to malignant arrhythmias in hyperkalemia, drug-induced QTc prolongation, WPW, and arrhy
This review aims to draw the attention of physicians confronted with cardiac emergencies to some specific ECG pathomorphologies in acute cor …
Understanding arrhythmogenic right ventricular cardiomyopathy.
Welkie R. Welkie R. JAAPA. 2023 May 1;36(5):1-6. doi: 10.1097/01.JAA.0000918764.35264.75. JAAPA. 2023. PMID: 37097786 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiac disease characterized by fibrofatty replacement of myocardial tissue and is an important cause of ventricular dysrhythmias, ventricular dysfunction, and sudden cardia
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiac disease characterized by fibrofatty repl
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
169 results