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204 Magnetic resonance imaging findings in early arrhythmogenic right ventricular dysplasia
Calkins Hugh +5 more
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Corrigendum to: Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis. [PDF]
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Arrhythmogenic right ventricular dysplasia/cardiomyopathy
Cardiology in the Young, 2017AbstractArrhythmogenic right ventricular dysplasia/cardiomyopathy is an inherited cardiomyopathy characterised by ventricular arrhythmias and an increased risk of sudden cardiac death. Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnosis is based on criteria that take into account electrical and structural cardiac abnormalities, as well ...
Gabriela M, Orgeron, Jane E, Crosson
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Arrhythmogenic right ventricular dysplasia
International Journal of Cardiology, 1996Right ventricular dysplasia is a primary disorder of the right ventricular myocardium characterised by a progressive replacement by adipose or fibrous tissue, proceeding from the epicardium towards the endocardium. Right ventricular dysplasia with the predominant clinical manifestation of an arrhythmia of right ventricular origin is defined as ...
A, Chauhan, R S, More
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Arrhythmogenic Right Ventricular Dysplasia
Current Treatment Options in Cardiovascular Medicine, 2010Arrhythmogenic right ventricular dysplasia (ARVD) is a genetic disorder that is characterized by ventricular arrhythmias and structural abnormalities of the right ventricle. Due to significant heterogeneity in its manifestation, the diagnosis of ARVD is challenging and requires a multifaceted approach to patient evaluation.
Harsh C, Patel, Hugh, Calkins
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Arrhythmogenic right ventricular dysplasia/cardiomyopathy
Heart & Lung, 2001Arrhythmogenic right ventricular dysplasia (ARVD/C) is one cause of death in young adults in the United States, representing approximately 17% of all ARVD/C cases reported. This study presents 2 cases of ARVD/C diagnosed at a central Texas hospital and reviews the literature regarding this disease. The diagnosis, histology, presentation, prognosis, and
T C, Harrison, D, Kessler
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Arrhythmogenic right ventricular dysplasia/cardiomyopathy
Current Cardiology Reports, 2005Arrhythmogenic right ventricular dysplasia/cardiomyopathy is recognized as an important cause of death in young patients, particularly athletes. In the past 5 years, cardiac MRI techniques have evolved rapidly in an attempt to improve the noninvasive diagnosis of this disorder.
Victor A, Ferrari +2 more
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Arrhythmogenic Right Ventricular Dysplasia
Progress in Cardiovascular Diseases, 2008Arrhythmogenic right ventricular dysplasia (ARVD) is an inherited cardiomyopathy characterized by ventricular arrhythmias and structural abnormalities of the right ventricle (RV). ARVD results from progressive replacement of right ventricular myocardium with fatty and fibrous tissue.
Palaniappan, Muthappan, Hugh, Calkins
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Arrhythmogenic right ventricular dysplasia.
Journal of insurance medicine (New York, N.Y.), 2005Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that is characterized by fibrofatty replacement of the right ventricle and is an important cause of ventricular arrhythmias in younger people.
G, Fontaine +5 more
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International Journal of Sports Medicine, 2019
Competitive sports and intensive exercise are associated with adverse outcomes in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C).
A. Müssigbrodt +12 more
semanticscholar +1 more source
Competitive sports and intensive exercise are associated with adverse outcomes in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C).
A. Müssigbrodt +12 more
semanticscholar +1 more source

