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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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:ESC Heart Fail
Hauptverfasser: Adam, Robert Daniel, Coriu, Daniel, Jercan, Andreea, Bădeliţă, Sorina, Popescu, Bogdan A., Damy, Thibaud, Jurcuţ, Ruxandra
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley and Sons Inc. 2021
Schlagworte:
Online Zugang: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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