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Understanding arrhythmogenic right ventricular cardiomyopathy
JAAPA, 2023ABSTRACT Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiac disease characterized by fibrofatty replacement of myocardial tissue and is an important cause of ventricular dysrhythmias, ventricular dysfunction, and sudden cardiac death.
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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 Cardiomyopathy
2020Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a kind of inherited cardiomyopathy that predominantly affects the right ventricle. Although early detection and treatment is of vital importance, the diagnosis of ARVC right now remains challenging.
Jian Wang, Yining Wang, Zheng-yu Jin
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Arrhythmogenic right ventricular dysplasia/cardiomyopathy
Expert Review of Cardiovascular Therapy, 2008Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a cardiac disease characterized by fibrofatty replacement of the cardiac myocytes. Patients with ARVD/C frequently present with ventricular tachycardia and many are thought to have sudden cardiac death as the initial manifestation of the disease.
Hicham Z, El Masry, Anil V, Yadav
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Arrhythmogenic right ventricular cardiomyopathy: An update
Cardiovascular Pathology, 2001Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease that predominantly affects the right ventricle (RV). The main pathologic feature is the progressive loss of RV myocardium and its replacement by fibrofatty tissue. The condition was initially believed to be a developmental defect of the RV myocardium, leading to
THIENE, GAETANO, BASSO, CRISTINA
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Genetics of arrhythmogenic right ventricular cardiomyopathy
Current Opinion in Cardiology, 2002Recent advances in molecular genetics of arrhythmogenic right ventricular cardiomyopathy (ARVD) are reviewed. In particular, the finding of mutations in the gene coding for cardiac ryanodine receptor (hRYR2), both in patients affected with ARVD2 and in patients affected with catecholaminergic ventricular arrhythmias or with familial ventricular ...
DANIELI, GIAN ANTONIO +1 more
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Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy
Cardiovascular Pathology, 2010Arrhythmogenic right ventricular cardiomyopathy (ARVC) represents an inherited cardiomyopathy that manifests clinically with malignant ventricular arrhythmias, sudden cardiac death, and less commonly heart failure. The condition is characterized by replacement of the myocardium, primarily of the right ventricle, with fibrofatty tissue.
Jason D, Roberts +3 more
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Arrhythmogenic right-ventricular dysplasia/cardiomyopathy
Current Opinion in Cardiology, 2006Arrhythmogenic right-ventricular dysplasia is a rare inherited disease characterized by right-ventricular dysfunction and ventricular arrhythmias. The purpose of this article is to review recent developments concerning the diagnosis, genetics, and management of patients with this disease.In the past few years important new information has emerged ...
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Arrhythmogenic right ventricular cardiomyopathy
The Lancet, 2015Jose Maria, Lopez-Ayala +3 more
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Arrhythmogenic right ventricular cardiomyopathy
The Journal of Pathology, 1993A H, Lee, J M, Morgan, P J, Gallagher
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