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

Year Number of Results
1991 1
1995 3
1996 2
1998 1
2000 2
2001 1
2003 2
2005 1
2006 1
2007 1
2008 3
2009 3
2010 3
2011 1
2012 1
2013 1
2014 4
2015 2
2016 2
2017 3
2018 2
2019 2
2020 1
2021 1
2023 0

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41 results

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Page 1
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.
Family physicians should be alert for acquired variants of cardiomyopathy, including peripartum and stress-induced cardiomyopathy, as well as rare variants, such as arrhythmogenic right ventricular dysplasia and left ventricular noncompaction. . …
Family physicians should be alert for acquired variants of cardiomyopathy, including peripartum and stress-induced cardiomyopathy, as well a …
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.
Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (arrhythmogenic right ventricular cardiomyopathy), they lacked sensitivity for identification of the expanding phenotypic spe …
Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (ar …
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 …
Arrhythmogenic right ventricular dysplasia.
Fontaine G. Fontaine G. Curr Opin Cardiol. 1995 Jan;10(1):16-20. doi: 10.1097/00001573-199501000-00004. Curr Opin Cardiol. 1995. PMID: 7787258 Review.
Arrhythmogenic right ventricular dysplasia is a relatively newly described clinical entity that is more and more frequently recognized. ...In some patients, a superimposed inflammatory process mixed with the pattern of arrhythmogenic right …
Arrhythmogenic right ventricular dysplasia is a relatively newly described clinical entity that is more and more …
Arrhythmogenic right ventricular dysplasia.
Anderson EL. Anderson EL. Am Fam Physician. 2006 Apr 15;73(8):1391-8. Am Fam Physician. 2006. PMID: 16669561 Free article. Review.
Arrhythmogenic right ventricular dysplasia (ARVD) is a disorder in which normal myocardium is replaced by fibrofatty tissue. This disorder usually involves the right ventricle, but the left ventricle and septum also may be affected. ...
Arrhythmogenic right ventricular dysplasia (ARVD) is a disorder in which normal myocardium is replaced by fibrof …
Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Hershberger RE, Cowan J, Morales A, Siegfried JD. Hershberger RE, et al. Circ Heart Fail. 2009 May;2(3):253-61. doi: 10.1161/CIRCHEARTFAILURE.108.817346. Circ Heart Fail. 2009. PMID: 19808347 Free PMC article. Review.
This review focuses on the genetic cardiomyopathies: principally dilated cardiomyopathy, with salient features of hypertrophic cardiomyopathy and arrhythmogenic right ventricular dysplasia/cardiomyopathy, regarding genetic etiology, genetic testing, an …
This review focuses on the genetic cardiomyopathies: principally dilated cardiomyopathy, with salient features of hypertrophic cardiomyopath …
Arrhythmogenic right ventricular cardiomyopathy 2012: diagnostic challenges and treatment.
Marcus FI, Abidov A. Marcus FI, et al. J Cardiovasc Electrophysiol. 2012 Oct;23(10):1149-53. doi: 10.1111/j.1540-8167.2012.02412.x. Epub 2012 Aug 21. J Cardiovasc Electrophysiol. 2012. PMID: 22909229 Review.
The most common presentation of arrhythmogenic right ventricular cardiomyopathy (ARVC) is palpitations or ventricular tachycardia (VT) of left bundle branch morphology in a young or middle-aged individual. The 12-lead electrocardiogram may be normal or …
The most common presentation of arrhythmogenic right ventricular cardiomyopathy (ARVC) is palpitations or ventricula …
Sudden cardiac death owing to arrhythmogenic right ventricular cardiomyopathy: Two case reports and systematic literature review.
Mu J, Zhang G, Xue D, Xi M, Qi J, Dong H. Mu J, et al. Medicine (Baltimore). 2017 Nov;96(47):e8808. doi: 10.1097/MD.0000000000008808. Medicine (Baltimore). 2017. PMID: 29381985 Free PMC article. Review.
BACKGROUND AND OBJECTIVE: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is increasingly recognized in forensic practice with controversial diagnosis. ...Exercise, acute stress, increased cardiac workload, and ethanol are frequently involved. The mean …
BACKGROUND AND OBJECTIVE: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is increasingly recognized in forensic …
Clinical classification of rare cardiac arrhythmogenic and conduction disorders, and rare arrhythmias.
Podolec P, Baranchuk A, Brugada J, Kukla P, Lelakowski J, Kopeć G, Rubiś P, Stępniewski J, Podolec J, Komar M, Tomkiewicz-Pająk L, Matusik PT. Podolec P, et al. Pol Arch Intern Med. 2019 Mar 29;129(3):154-159. doi: 10.20452/pamw.4451. Epub 2019 Feb 19. Pol Arch Intern Med. 2019. PMID: 30778019 Free article. Review.
OBJECTIVES The aim of this paper is to provide an updated classification of rare arrhythmogenic and conduction disorders, and rare arrhythmias (RACDRAs). METHODS We performed a search for RACDRAs using the Orphanet inventory of rare diseases, which includes diseases with a …
OBJECTIVES The aim of this paper is to provide an updated classification of rare arrhythmogenic and conduction disorders, and rare ar …
41 results