Results 161 to 170 of about 14,748 (188)
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Bradyarrhythmias in Arrhythmogenic Right Ventricular Cardiomyopathy
The American Journal of Cardiology, 2019Less is known about bradyarrhythmias in arrhythmogenic right ventricular cardiomyopathy (ARVC). This cross-sectional study aimed to assess the prevalence and clinical significance of bradyarrhythmias in ARVC. From May 1995 to December 2017, bradyarrhythmias including sick sinus syndrome, atrioventricular block, and intraventricular conductional block ...
Erpeng Liang +9 more
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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
Herz, 2012There have been major advances in recent years in the clinical setting of arrhythmogenic right ventricular cardiomyopathy, including new diagnostic criteria, a changing spectrum of the disease with even left dominant forms, the role of cardiac magnetic resonance and electroanatomic mapping, the expanding use of genetic screening and the existence of ...
THIENE, GAETANO +4 more
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Pathology and Pathogenesis of Arrhythmogenic Right Ventricular Cardiomyopathy
Herz, 2000Arrhythmogenic right ventricular cardiomyopathy is a primary heart muscle disease characterized by progressive myocardial atrophy of the right ventricle, with transmural fatty or fibrofatty replacement, either segmental or diffuse, accounting for electrical instability at risk of life-threatening ventricular arrhythmias.
THIENE, GAETANO +4 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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Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy
2001Molecular genetics of arrhythmogenic right ventricular ...
RAMPAZZO, ALESSANDRA +4 more
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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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