Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences

AIMS: The dilated cardiomyopathy (DCM) phenotype is the result of combined genetic and acquired triggers. Until now, clinical decision-making in DCM has mainly been based on ejection fraction (EF) and NYHA classification, not considering the DCM heterogenicity. The present study aimed to identify pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Verdonschot, Job A J, Merlo, Marco, Dominguez, Fernando, Wang, Ping, Henkens, Michiel T H M, Adriaens, Michiel E, Hazebroek, Mark R, Masè, Marco, Escobar, Luis E, Cobas-Paz, Rafael, Derks, Kasper W J, van den Wijngaard, Arthur, Krapels, Ingrid P C, Brunner, Han G, Sinagra, Gianfranco, Garcia-Pavia, Pablo, Heymans, Stephane R B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813623/
https://www.ncbi.nlm.nih.gov/pubmed/33156912
http://dx.doi.org/10.1093/eurheartj/ehaa841

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813623/
https://www.ncbi.nlm.nih.gov/pubmed/33156912
http://dx.doi.org/10.1093/eurheartj/ehaa841

Ejemplares similares