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

Year Number of Results
1984 1
1987 1
1989 2
1990 2
1991 3
1992 2
1993 3
1994 6
1995 13
1996 9
1997 8
1998 15
1999 10
2000 21
2001 18
2002 22
2003 14
2004 23
2005 37
2006 24
2007 18
2008 30
2009 32
2010 29
2011 19
2012 34
2013 29
2014 40
2015 54
2016 40
2017 45
2018 30
2019 32
2020 34
2021 31
2022 32
2023 15

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718 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. ...Risk stratification of patients with ARVC …
Arrhythmogenic right ventricular cardiomyopathy (ARVC) encompasses a group of conditions characterized by rig …
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, inc …
Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can cause exertional dyspnea, presyncope, atypical c …
Arrhythmogenic right ventricular cardiomyopathy: a focused update on diagnosis and risk stratification.
Bosman LP, Te Riele ASJM. Bosman LP, et al. Heart. 2022 Jan;108(2):90-97. doi: 10.1136/heartjnl-2021-319113. Epub 2021 May 14. Heart. 2022. PMID: 33990412 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterised by fibrofatty replacement of predominantly the right ventricle and high risk of ventricular arrhythmias and sudden cardiac death (S …
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterised by fi …
Clinical Diagnosis, Imaging, and Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: JACC State-of-the-Art Review.
Gandjbakhch E, Redheuil A, Pousset F, Charron P, Frank R. Gandjbakhch E, et al. J Am Coll Cardiol. 2018 Aug 14;72(7):784-804. doi: 10.1016/j.jacc.2018.05.065. J Am Coll Cardiol. 2018. PMID: 30092956 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited cardiomyopathy that can lead to sudden cardiac death and heart failure. ...Advances in genetics have enlarged the clinical spectrum of the disease, highlig …
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited cardiomyopathy …
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 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 i …
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in you …
Cardiomyopathy and pregnancy.
Schaufelberger M. Schaufelberger M. Heart. 2019 Oct;105(20):1543-1551. doi: 10.1136/heartjnl-2018-313476. Epub 2019 Jul 15. Heart. 2019. PMID: 31308064 Free PMC article. Review.
The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy. Rare types are arrhythmogenic right ventricular, restrictive, Takotsubo and left ventricular non-compaction cardiomyopathies. ...Complications include different types …
The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy. Rare types are arrhythmogenic right ve …
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 cli …
BACKGROUND: In 1994, an International Task Force proposed criteria for the clinical diagnosis of arrhythmogenic right ventr …
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 establi …
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare, heritable myocardial disease associated with t …
Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy.
Corrado D, Zorzi A, Cipriani A, Bauce B, Bariani R, Beffagna G, De Lazzari M, Migliore F, Pilichou K, Rampazzo A, Rigato I, Rizzo S, Thiene G, Perazzolo Marra M, Basso C. Corrado D, et al. J Am Heart Assoc. 2021 Sep 21;10(18):e021987. doi: 10.1161/JAHA.121.021987. Epub 2021 Sep 17. J Am Heart Assoc. 2021. PMID: 34533054 Free PMC article. Review.
Criteria for diagnosis of arrhythmogenic cardiomyopathy (ACM) were first proposed in 1994 and revised in 2010 by a Task Force. Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (a …
Criteria for diagnosis of arrhythmogenic cardiomyopathy (ACM) were first proposed in 1994 and revised in 2010 by a Task Force. …
718 results