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Progress and challenges in the treatment of cardiac amyloidosis: a review of the literature

Cardiac amyloidosis is a restrictive cardiomyopathy determined by the accumulation of amyloid, which is represented by misfolded protein fragments in the cardiac extracellular space. The main classification of systemic amyloidosis is determined by the amyloid precursor proteins causing a very hetero...

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Detalles Bibliográficos
Autores principales: Adam, Robert Daniel, Coriu, Daniel, Jercan, Andreea, Bădeliţă, Sorina, Popescu, Bogdan A., Damy, Thibaud, Jurcuţ, Ruxandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318516/
https://www.ncbi.nlm.nih.gov/pubmed/34089308
http://dx.doi.org/10.1002/ehf2.13443