Abstract
Cardiomyopathies are diseases of the heart characterized by ventricular dysfunction that is not due to secondary causes such as hypertension, congenital, valvular, coronary, arterial, or pericardial abnormalities. They are described as primary cardiomyopathies if the origin of cardiac dysfunction is unknown, and as secondary or specific cardiomyopathies if the heart is involved by specific infectious, metabolic, neuromuscular or toxic diseases. According to the new definition of the WHO, primary cardiomyopathies are classified as dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy [1].
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Kühl, U., Noutsias, M., Schultheiss, HP. (1997). Immunohistochemical Analysis of Inflammatory Heart Disease. In: Schultheiss, HP., Schwimmbeck, P. (eds) The Role of Immune Mechanisms in Cardiovascular Disease. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-60463-8_10
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DOI: https://doi.org/10.1007/978-3-642-60463-8_10
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