Reversible dilated cardiomyopathy: into the thaumaturgy of the heart - Part 2

Dilated cardiomyopathy (DCM) is a genetic or acquired heart muscle disorder characterized by dilation and impaired contraction of one or both ventricles. In the acquired forms of the disease, if the pathogenic agent is persistent, undiagnosed or untreated, permanent ultrastructural and morphological...

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Bibliographic Details
Main Authors: Giovanni Quarta, Raffaele Coppini, Pier Lambiase, Pablo Garcia-Pavia, Alice Calabrese, Anna Maria Iorio, Niccolò Maurizi, Maria Iascone, Antonello Gavazzi, Iacopo Olivotto, Michele Senni
Format: Article
Language:English
Published: MDPI AG 2016-10-01
Series:Cardiogenetics
Subjects:
Online Access:http://www.pagepressjournals.org/index.php/cardiogen/article/view/5862