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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
1994 1
1995 1
1996 1
1997 1
1998 1
1999 1
2000 4
2001 2
2002 2
2003 3
2004 4
2005 3
2006 2
2007 1
2008 3
2009 5
2010 5
2011 1
2012 2
2013 2
2014 5
2015 5
2016 4
2017 6
2019 5
2020 2
2021 1
2022 7
2023 3
2024 1

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80 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 aims to
Arrhythmogenic right ventricular cardiomyopathy (ARVC) encompasses a group of conditions characterized by right
Exercise and Arrhythmogenic Right Ventricular Cardiomyopathy.
Prior D, La Gerche A. Prior D, et al. Heart Lung Circ. 2020 Apr;29(4):547-555. doi: 10.1016/j.hlc.2019.12.007. Epub 2019 Dec 26. Heart Lung Circ. 2020. PMID: 31964580 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a group of cardiomyopathies associated with ventricular arrhythmias predominantly arising from the right ventricle, sudden cardiac death and right ventricular failure, cause
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a group of cardiomyopathies associated with ventricular
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. ...A …
Dilated and hypertrophic cardiomyopathy phenotypes share an incidence of 60% and 25%, respectively. Arrhythmogenic right ve
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a review of molecular and clinical literature.
Murray B. Murray B. J Genet Couns. 2012 Aug;21(4):494-504. doi: 10.1007/s10897-012-9497-7. Epub 2012 Mar 17. J Genet Couns. 2012. PMID: 22426942 Review.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is heritable cardiomyopathy that may result in arrhythmia, heart failure, and sudden cardiac death (SCD). ...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is heritable cardiomyopathy that may result i
Arrhythmogenic right ventricular cardiomyopathy: diverse substrate characteristics and ablation outcome.
Cheng WH, Chung FP, Lin YJ, Lo LW, Chang SL, Hu YF, Tuan TC, Chao TF, Liao JN, Lin CY, Chang TY, Kuo L, Wu CI, Liu CM, Liu SH, Chen SA. Cheng WH, et al. Rev Cardiovasc Med. 2021 Dec 22;22(4):1295-1309. doi: 10.31083/j.rcm2204136. Rev Cardiovasc Med. 2021. PMID: 34957771 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy caused by defective desmosomal proteins. The typical histopathological finding of ARVC is characterized by progressive fibrofatty infiltration of the right ventricle
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy caused by defective desmosomal pr
Catheter Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy.
Gasperetti A, Tandri H. Gasperetti A, et al. Card Electrophysiol Clin. 2022 Dec;14(4):679-683. doi: 10.1016/j.ccep.2022.08.004. Card Electrophysiol Clin. 2022. PMID: 36396184 Review.
Arrhythmogenic right ventricular cardiomyopathy is an inherited desmosomal myopathy characterized by progressive fibrofatty replacement of the myocardium, right ventricular enlargement, and malignant ventricular arrhythmias. Ventricula
Arrhythmogenic right ventricular cardiomyopathy is an inherited desmosomal myopathy characterized by progressive fibrof
Management of arrhythmogenic right ventricular cardiomyopathy.
Silvano M, Mastella G, Zorzi A, Migliore F, Pilichou K, Bauce B, Rigato I, Perazzolo Marra M, Iliceto S, Thiene G, Basso C, Corrado D. Silvano M, et al. Minerva Med. 2016 Aug;107(4):194-216. Epub 2016 May 17. Minerva Med. 2016. PMID: 27186923 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically determined heart muscle disorder, predisposing to sudden cardiac death (SCD), particularly in young patients and athletes. Pathological features include loss of myocytes and fibrofatty re
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically determined heart muscle disorder, predisposing
Hereditary Syndromes of Sudden Cardiac Death.
Berberian JG. Berberian JG. Emerg Med Clin North Am. 2022 Nov;40(4):651-662. doi: 10.1016/j.emc.2022.06.005. Epub 2022 Oct 7. Emerg Med Clin North Am. 2022. PMID: 36396213 Review.
Current and future role of echocardiography in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Mast TP, Teske AJ, Doevendans PA, Cramer MJ. Mast TP, et al. Cardiol J. 2015;22(4):362-74. doi: 10.5603/CJ.a2015.0018. Epub 2015 Mar 19. Cardiol J. 2015. PMID: 25786767 Free article. Review.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited progressive cardiomyopathy, clinically characterized by ventricular arrhythmias and increased risk of sudden cardiac death. ...Relatively novel echocardiographic
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited progressive cardiomyopathy, c
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. ...The main questions regarding the risk stratification and the therapeutic strategy in A
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited heart muscle disease that occ
80 results