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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]
Cardiovasc Res, 2017 europepmc +1 more source
204 Magnetic resonance imaging findings in early arrhythmogenic right ventricular dysplasia
Journal of Cardiovascular Magnetic Resonance, 2008 Calkins Hugh +5 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
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
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
The American Journal of Emergency Medicine, 2001Right ventricular dysplasia (RVD) is a disease entity of unknown cause that is characterised by partial or total replacement of RV-muscle by adipose or fibrous tissue. It is a well-recognized cause of arrhythmia and premature sudden death, but usually underdiagnosed.
A J, Kinsara, L, Zaman, A, Gorgels
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Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Anesthesiology, 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
G, Fontaine +4 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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