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Arrhythmogenic RV Cardiomyopathy/Dysplasia Recent Advances /

This book covers all aspects (biological, pathological, genetic, clinical and therapeutical) of arrhythmogenic right ventricular cardiomyopathy/dysplasia, a recent cardiomyopathy which represents a very high risk of sudden death in the young and in athletes. The monograph presents the results of 5-y...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Marcus, Frank I. (Editor ), Nava, Andrea (Editor ), Thiene, Gaetano (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Milano : Springer Milan : Imprint: Springer, 2007.
Edición:1st ed. 2007.
Temas:
Acceso en línea:Texto Completo

MARC

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245 1 0 |a Arrhythmogenic RV Cardiomyopathy/Dysplasia  |h [electronic resource] :  |b Recent Advances /  |c edited by Frank I. Marcus, Andrea Nava, Gaetano Thiene. 
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300 |a XIII, 217 p.  |b online resource. 
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505 0 |a Introduction: Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Clarified -- Advances in Genetics: Dominant Forms -- Advances in Genetics: Recessive Forms -- Genotype-Phenotype Correlations -- Autopsy and Endomyocardial Biopsy Findings -- Cell Adhesion Pathology -- Ultrastructural Substrates -- Transgenic Animal Models -- Spontaneous Animal Models -- Possible Causative or Contributing Role of Viruses -- Diagnosis: Task Force Criteria including Modifications for Family Members -- Strengths and Weaknesses of the Task Force Criteria - Proposed Modifications -- Idiopathic Right Ventricular Outflow Tract Tachycardia -- Electrocardiographic Manifestations -- Echocardiography -- MR and CT Imaging -- Diagnostic Role of Angiography -- Electrophysiologic Study including Electroanatomic Mapping -- Risk Stratification and Antiarrhythmic Drug Therapy -- Catheter Ablation of Ventricular Tachycardia -- The Role of the Implantable Cardiac Defibrillator in the Management -- Management of Heart Failure -- Sudden Death in Young Athletes. 
520 |a This book covers all aspects (biological, pathological, genetic, clinical and therapeutical) of arrhythmogenic right ventricular cardiomyopathy/dysplasia, a recent cardiomyopathy which represents a very high risk of sudden death in the young and in athletes. The monograph presents the results of 5-year research program on ARVC/D supported by grants of both the European Commission and the NIH, which enabled the discovery of seven disease-causing genes, thus opening new avenues for the early identification of affected patients and for sudden death prevention. A panel of top scientists, both European and Americans, contributed to this volume, which will be an essential reference for professionals and residents in cardiology, radiology, human genetics, and sport medicine. 
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