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Year Number of Results
1996 1
1998 1
1999 1
2000 3
2001 1
2002 2
2003 3
2004 1
2005 4
2006 1
2007 3
2008 2
2009 1
2010 3
2011 1
2012 2
2013 2
2014 1
2015 2
2016 4
2017 10
2018 3
2019 1
2020 3
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2023 2
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57 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
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
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
Epicardial Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy.
Assis FR, Tandri H. Assis FR, et al. Card Electrophysiol Clin. 2020 Sep;12(3):329-343. doi: 10.1016/j.ccep.2020.05.005. Epub 2020 Jul 8. Card Electrophysiol Clin. 2020. PMID: 32771187 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease characterized by progressive fibrofatty replacement of the myocardium, right ventricular enlargement, and malignant ventricular arrhythmias. Ve
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease characterized by progressiv
Arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Thiene G, Corrado D, Basso C. Thiene G, et al. Orphanet J Rare Dis. 2007 Nov 14;2:45. doi: 10.1186/1750-1172-2-45. Orphanet J Rare Dis. 2007. PMID: 18001465 Free PMC article. Review.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a heart muscle disease clinically characterized by life-threatening ventricular arrhythmias. ...The pathology consists of a genetically determined dystrophy of the right
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a heart muscle disease clinically characte
Fibroblasts and the extracellular matrix in right ventricular disease.
Frangogiannis NG. Frangogiannis NG. Cardiovasc Res. 2017 Oct 1;113(12):1453-1464. doi: 10.1093/cvr/cvx146. Cardiovasc Res. 2017. PMID: 28957531 Free PMC article. Review.
Expansion of fibroblasts and extracellular matrix protein deposition are prominent features of arrhythmogenic right ventricular cardiomyopathies and may be implicated in the pathogenesis of arrhythmic events. Prevailing conceptual paradigms on right
Expansion of fibroblasts and extracellular matrix protein deposition are prominent features of arrhythmogenic right ventric
MicroRNAs in right ventricular remodelling.
Batkai S, Bär C, Thum T. Batkai S, et al. Cardiovasc Res. 2017 Oct 1;113(12):1433-1440. doi: 10.1093/cvr/cvx153. Cardiovasc Res. 2017. PMID: 28957533 Review.
Right ventricular (RV) remodelling is a lesser understood process of the chronic, progressive transformation of the RV structure leading to reduced functional capacity and subsequent failure. ...The role of microRNAs in diseases affecting the left ventricle has been
Right ventricular (RV) remodelling is a lesser understood process of the chronic, progressive transformation of the RV structu
Arrhythmogenic right ventricular dysplasia/cardiomyopathy. A review and update.
Francés RJ. Francés RJ. Int J Cardiol. 2006 Jun 28;110(3):279-87. doi: 10.1016/j.ijcard.2005.07.004. Epub 2005 Aug 15. Int J Cardiol. 2006. PMID: 16099519 Review.
The arrhythmogenic right ventricular dysplasia/cardiomyopathy is an important cause of sudden arrhythmic death, often exertional, in young individuals and athletes. ...The two-dimensional echocardiography, magnetic resonance imaging, computerized tomog …
The arrhythmogenic right ventricular dysplasia/cardiomyopathy is an important cause of sudden arrhythmic death, …
[Arrhythmogenic right ventricular cardiomyopathy/dysplasia. Literature review and case report].
Camargo-Ariza WA, Galvis-Blanco SJ, Camacho-Enciso TDP, Quiroz-Romero CA, Bermudez-Echeverry JJ. Camargo-Ariza WA, et al. Arch Cardiol Mex. 2018 Jan-Mar;88(1):51-59. doi: 10.1016/j.acmx.2017.05.001. Epub 2017 Jun 13. Arch Cardiol Mex. 2018. PMID: 28623036 Review. Spanish.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia is an inherited autosomal dominant disease, with an estimated prevalence of 1:2,500 to 1:5,000, being higher in males (3:1). ...A comprehensive review of the patient's medical records was perfor
Arrhythmogenic right ventricular cardiomyopathy/dysplasia is an inherited autosomal dominant disease, with an es
Cardiac Imaging In Athletes.
Khan AA, Safi L, Wood M. Khan AA, et al. Methodist Debakey Cardiovasc J. 2016 Apr-Jun;12(2):86-92. doi: 10.14797/mdcj-12-2-86. Methodist Debakey Cardiovasc J. 2016. PMID: 27486490 Free PMC article. Review.
The hemodynamic effects of endurance and strength training exercise lead to these adaptations. Any abnormalities in chamber dilatation and left ventricular function usually normalize with cessation of exercise. Athletic heart syndrome is rare and should be differentiated f …
The hemodynamic effects of endurance and strength training exercise lead to these adaptations. Any abnormalities in chamber dilatation and l …
57 results