Titlebook: Arrhythmogenic RV Cardiomyopathy/Dysplasia; Recent Advances Frank I. Markus,Andrea Nava,Gaetano Thiene Book 20071st edition Springer-Verlag

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Benedikt Cramer,Hans-Ulrich Humpfar involvement, with relative sparing of the septum. Familial disease is common, with autosomal dominant inheritance and incomplete penetrance; a recessive form is described. Presentation with arrhythmias and sudden death is common, particularly in the young” [.].

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Book 20071st edition muscle d- ease which is a major threat to the life of affected young people. It summarizes ne- ly 25 years of investigation on the etiology, genetics, pathology, clinical features, - agnosis, and treatment of ARVC/D. In particular, a 5-year research program supported by grants from both the Europea

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Science Networks. Historical Studiesng myocyte fibers provide the morphological substrate for re-entrant arrhythmias and regional (segmental) or global (diffuse) abnormalities of RV structure and function. In the advanced stages of ARVC/D, clinical signs of right or global heart failure and left ventricular (LV) involvement may develop [.].

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Introduction: Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Clarified,major advancements in the basic knowledge of the disease as well as a better understanding of the diagnosis and treatment. A workshop was held in Venice, Italy on October 3, 2005, where research on various aspects of this disease, both biological and clinical was presented.

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