Titlebook: Advances in Cardiomyopathies; Proceedings of the I Fulvio Camerini,Antonello Gavazzi,Renata Maria Conference proceedings 1998 Springer-Verl

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Kyle James Downey,Margaret Rush Drekerhere have not yet been any prospective randomized therapeutic studies with precisely characterized patient populations. Ultimately decisive for the development of adequate therapeutic strategies, however, is a precise clinical evaluation of the patients to be treated. Besides documenting the clinica

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https://doi.org/10.1007/978-88-470-2155-6Dilated cardiomyopathy; circulation; familial cardiomyopathies; genetics; heart; heart transplantation; hy

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Scripting, AI, and Depth (and Death),The morphological, functional, and genetic abnormalities are heterogeneous in different patient populations with hypertrophie cardiomyopathy (HCM) [1–8]; as a consequence, the natural history and the clinical course are extremely variable and prognostic evaluation is a challenging task in the individual patient.

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Overview: 978-88-470-2181-5978-88-470-2155-6

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https://doi.org/10.1007/978-1-4302-0980-5asymptomatic course to severe heart failure and cardiac arrest. Ventricular arrhythmias, palpitations and syncope are frequent signs and symptoms. Sudden, unexpected cardiac arrest is a pending catastrophe in the natural history of HCM.