Results 61 to 70 of about 13,561 (98)
Some of the next articles are maybe not open access.
Arrhythmogenic Right Ventricular Cardiomyopathy
New England Journal of Medicine, 2017Abstract Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heredo-familial heart muscle disease characterized by progressive myocardial atrophy with fibrofatty replacement. It is a rare disease with an estimated prevalence of 1:2000 to 1:5000.
Corrado, Domenico +2 more
openaire +7 more sources
Arrhythmogenic Right Ventricular Cardiomyopathy
Heart Failure Clinics, 2010Arrhythmogenic right ventricular cardiomyopathy (ARVC) originally emerged as a pathologic diagnosis based on distinctive autopsy findings in cases of premature sudden death. Subsequently these characteristic pathologic features were associated with ventricular tachycardia of right ventricular origin and syncope.
Patrick T, Ellinor +2 more
openaire +5 more sources
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
openaire +4 more sources
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
openaire +4 more sources
Arrhythmogenic Right Ventricular Cardiomyopathy Diagnosis
Cardiology in Review, 2020Arrhythmogenic right ventricular cardiomyopathy, formerly called “arrhythmogenic right ventricular dysplasia,” is an under-recognized clinical entity characterized by ventricular arrhythmias and a characteristic ventricular pathology. Diagnosis is often difficult due to the nonspecific nature of the disease and the broad spectrum of phenotypic ...
Amer, Sayed +6 more
openaire +2 more sources
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.
openaire +2 more sources
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
openaire +2 more sources