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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Am Heart Assoc
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: John Wiley and Sons Inc. 2015
विषय:
Original Research
ऑनलाइन पहुंच: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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