Results 171 to 180 of about 7,984 (209)

Arrhythmogenic Right Ventricular Dysplasia

Current Treatment Options in Cardiovascular Medicine, 2010
Arrhythmogenic 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, 2001
Arrhythmogenic 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, 2005
Arrhythmogenic 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, Craig H, Scott, Cristina, Basso   +2 more
openaire   +4 more sources

Arrhythmogenic Right Ventricular Dysplasia

Progress in Cardiovascular Diseases, 2008
Arrhythmogenic 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
openaire   +2 more sources

Arrhythmogenic right ventricular dysplasia.

Journal of insurance medicine (New York, N.Y.), 2005
Arrhythmogenic 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, J L, Hebert, C, Prost-Squarcioni, P, Fornes, R, Frank, D, Thomas   +5 more
  +6 more sources

Arrhythmogenic right ventricular dysplasia/cardiomyopathy

Cardiology in the Young, 2017
AbstractArrhythmogenic 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/cardiomyopathy

Expert Review of Cardiovascular Therapy, 2008
Arrhythmogenic 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
openaire   +2 more sources

Arrhythmogenic right-ventricular dysplasia/cardiomyopathy

Current Opinion in Cardiology, 2006
Arrhythmogenic 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 ...
openaire   +2 more sources

[Arrhythmogenic right ventricular dysplasia].

Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2004
Arrhythmogenic right ventricular dysplasia (ARVD) is a new form of cardiomyopathy probably more frequent than commonly reported. The incidence is unknown. ARVD is a heart muscle disorder of unknown cause that is characterised pathologically by fibro-fatty replacement of the right ventricular myocardium.
Carmen, Grigoriu, Doina, Butcovan, V, Astărăstoae   +2 more
openaire   +1 more source

[Arrhythmogenic right ventricular dysplasia].

Revue medicale de Liege, 2007
Arrhythmogenic right ventricular dysplasia is an unfrequent disease that associates ventricular tachycardia with left bundle branch block morphology and right ventricular fibro-fatty degeneration. The etiology, pathogenesis, criteria for diagnosis and treatment are discussed.
C, Garweg, P, Mélon, A, Waleffe, L, Piérard   +3 more
openaire   +1 more source