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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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Detalhes bibliográficos
Publicado no:ESC Heart Fail
Main Authors: Adam, Robert Daniel, Coriu, Daniel, Jercan, Andreea, Bădeliţă, Sorina, Popescu, Bogdan A., Damy, Thibaud, Jurcuţ, Ruxandra
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8318516/
https://ncbi.nlm.nih.gov/pubmed/34089308
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ehf2.13443
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