Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life‐Threatening Arrhythmias

BACKGROUND: Patients with dilated cardiomyopathy (DCM) may present with ventricular arrhythmias early in the disease course, unrelated to the severity of left ventricular dysfunction. These patients may be classified as having an arrhythmogenic DCM (AR‐DCM). We investigated the phenotype and natural...

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Detalhes bibliográficos
Publicado no:J Am Heart Assoc
Main Authors: Spezzacatene, Anita, Sinagra, Gianfranco, Merlo, Marco, Barbati, Giulia, Graw, Sharon L., Brun, Francesca, Slavov, Dobromir, Di Lenarda, Andrea, Salcedo, Ernesto E., Towbin, Jeffrey A., Saffitz, Jeffrey E., Marcus, Frank I., Zareba, Wojciech, Taylor, Matthew R. G., Mestroni, Luisa
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2015
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4845125/
https://ncbi.nlm.nih.gov/pubmed/26475296
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/JAHA.115.002149
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