Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry

Abstract Aims Dilated cardiomyopathy (DCM) is a complex disease where genetics interplay with extrinsic factors. This study aims to compare the phenotype, management, and outcome of familial DCM (FDCM) and non‐familial (sporadic) DCM (SDCM) across Europe. Methods and results Patients with DCM that w...

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ग्रंथसूची विवरण

मुख्य लेखकों:	Folkert W. Asselbergs, Arjan Sammani, Perry Elliott, Juan R. Gimeno, Luigi Tavazzi, Michael Tendera, Juan Pablo Kaski, Aldo P. Maggioni, Pawel P. Rubis, Ruxandra Jurcut, Tiina Heliö, Leonardo Calò, Gianfranco Sinagra, Marija Zdravkovic, Iacopo Olivotto, Aušra Kavoliūnienė, Cécile Laroche, Alida L.P. Caforio, Philippe Charron, Cardiomyopathy & Myocarditis Registry Investigators Group
स्वरूप:	Artigo
भाषा:	Inglês
प्रकाशित:	Oxford University Press 2021-02-01
श्रृंखला:	ESC Heart Failure
विषय:	Dilated cardiomyopathy Sporadic Familial Genetic Prognosis Europe
ऑनलाइन पहुंच:	https://doi.org/10.1002/ehf2.13100
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