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

Year Number of Results
1989 1
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1996 1
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2006 2
2007 2
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44 results

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Page 1
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
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
Radiofrequency Ablation in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC).
Romero J, Grushko M, Briceño DF, Natale A, Di Biase L. Romero J, et al. Curr Cardiol Rep. 2017 Sep;19(9):82. doi: 10.1007/s11886-017-0893-3. Curr Cardiol Rep. 2017. PMID: 28779285 Review.
PURPOSE OF REVIEW: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heritable form of cardiomyopathy, typically with autosomal dominant transmission, shown to be a defect in the cardiac desmosomes, with distinct regional and histopathological featu …
PURPOSE OF REVIEW: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heritable form of cardiomyopathy, typica …
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). ...
Arrhythmogenic cardiomyopathy (ACM) is a disease characterized by a progressive replacement of myocardium by fibro-adipose material,
Evolving spectrum of arrhythmogenic cardiomyopathy: Implications for Sports Cardiology.
Graziano F, Cipriani A, Balla D, Bondarev S, Marra MP, Bauce B, Vágó H, Corrado D, Zorzi A. Graziano F, et al. Clin Cardiol. 2023 Sep;46(9):1072-1081. doi: 10.1002/clc.24069. Epub 2023 Jun 25. Clin Cardiol. 2023. PMID: 37357443 Free PMC article. Review.
Arrhythmogenic cardiomyopathy (ACM) is a genetic heart muscle disease, structurally characterized by progressive fibro-fatty replacement of the normal myocardium and clinically by ventricular arrhythmias (VAs). Predominantly thanks to the use of cardiac magnetic res
Arrhythmogenic cardiomyopathy (ACM) is a genetic heart muscle disease, structurally characterized by progressive fibro-fatty replacem
Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Dysplasia.
Pathak RK, Garcia FC. Pathak RK, et al. Card Electrophysiol Clin. 2017 Mar;9(1):99-106. doi: 10.1016/j.ccep.2016.10.007. Epub 2016 Dec 27. Card Electrophysiol Clin. 2017. PMID: 28167090 Review.
Endocardial and epicardial electroanatomical mapping and ablation is a safe and effective therapy in the treatment of right ventricle arrhythmias occurring in the setting of arrhythmogenic right ventricular cardiomyopathy (ARVD). Careful mapping and ab …
Endocardial and epicardial electroanatomical mapping and ablation is a safe and effective therapy in the treatment of right ventricle …
Arrhythmogenic right ventricular cardiomyopathy/dysplasia: risk stratification and therapy.
Buja G, Estes NA 3rd, Wichter T, Corrado D, Marcus F, Thiene G. Buja G, et al. Prog Cardiovasc Dis. 2008 Jan-Feb;50(4):282-93. doi: 10.1016/j.pcad.2007.10.004. Prog Cardiovasc Dis. 2008. PMID: 18156007 Free PMC article. Review.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited heart muscle disease that occurs primarily in young and middle-age individuals. ...Heart failure may occur later in life secondary to slow, progressive loss of right
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited heart muscle disease that occ
Review on the genetics of arrhythmogenic right ventricular dysplasia.
Moric-Janiszewska E, Markiewicz-Loskot G. Moric-Janiszewska E, et al. Europace. 2007 May;9(5):259-66. doi: 10.1093/europace/eum034. Epub 2007 Mar 15. Europace. 2007. PMID: 17363426 Review.
Arrhythmogenic right ventricular dysplasia (ARVD) is a clinical and pathologic entity whose diagnosis rests on electrocardiographic and angiographic criteria; pathologic findings, replacement of ventricular myocardium with fatty and fibrous elem
Arrhythmogenic right ventricular dysplasia (ARVD) is a clinical and pathologic entity whose diagnosis rests on e
Arrhythmogenic right ventricular cardiomyopathy : Evolving from unique clinical features to a complex pathophysiological concept.
Paul M, Schulze-Bahr E. Paul M, et al. Herz. 2020 May;45(3):243-251. doi: 10.1007/s00059-020-04907-1. Herz. 2020. PMID: 32170341 Review. English.
Arrhythmogenic right ventricular cardiomyopathy (ARVC), an inherited heart muscle disease, is characterized by a progressive replacement of viable, in its classic form predominantly right ventricular myocardium by fibro-fatty tissue. ...Based on
Arrhythmogenic right ventricular cardiomyopathy (ARVC), an inherited heart muscle disease, is characterized by a progre
44 results