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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
2019 11
2020 2
2021 6
2022 7
2023 7
2024 3

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170 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.
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 …
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 …
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 …
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 …
Cardiomyopathies in children: An overview.
Tsatsopoulou A, Protonotarios I, Xylouri Z, Papagiannis I, Anastasakis A, Germanakis I, Patrianakos A, Nyktari E, Gavras C, Papadopoulos G, Meditskou S, Lazarou E, Miliou A, Lazaros G. Tsatsopoulou A, et al. Hellenic J Cardiol. 2023 Jul-Aug;72:43-56. doi: 10.1016/j.hjc.2023.02.007. Epub 2023 Mar 3. Hellenic J Cardiol. 2023. PMID: 36870438 Free article. Review.
Dilated and hypertrophic cardiomyopathy phenotypes share an incidence of 60% and 25%, respectively. Arrhythmogenic right ventricular cardiomyopathy (ARVC), restrictive cardiomyopathy, and left ventricular noncompaction are less commonly diagnosed. ...I …
Dilated and hypertrophic cardiomyopathy phenotypes share an incidence of 60% and 25%, respectively. Arrhythmogenic right ve …
Right ventricular remodeling in athletes and in arrhythmogenic cardiomyopathy.
Chivulescu M, Haugaa K, Lie ØH, Edvardsen T, Ginghină C, Popescu BA, Jurcut R. Chivulescu M, et al. Scand Cardiovasc J. 2018 Feb;52(1):13-19. doi: 10.1080/14017431.2017.1416158. Epub 2017 Dec 19. Scand Cardiovasc J. 2018. PMID: 29254378 Review.
OBJECTIVE: Changes in right ventricular (RV) structure and function following prolonged endurance training in athletes arise due to its unique anatomy and physiology. Arrhythmogenic cardiomyopathy (AC) should be differentiated from electrical, functional and …
OBJECTIVE: Changes in right ventricular (RV) structure and function following prolonged endurance training in athletes arise d …
Arrhythmogenic right ventricular cardiomyopathy in the pediatric population.
Cohen MI, Atkins MB. Cohen MI, et al. Curr Opin Cardiol. 2022 Jan 1;37(1):99-108. doi: 10.1097/HCO.0000000000000937. Curr Opin Cardiol. 2022. PMID: 34857718 Review.
PURPOSE OF REVIEW: Review the current state of the art of arrhythmogenic right ventricular cardiomyopathy (ARVC) diagnosis and risk stratification in the pediatric population. RECENT FINDINGS: ARVC is an inherited cardiomyopathy characterized by progressive m …
PURPOSE OF REVIEW: Review the current state of the art of arrhythmogenic right ventricular cardiomyopathy (ARVC) diagno …
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 …
170 results