Cargando…
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...
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 |
Ejemplares similares
-
Muscle involvement with pseudohypertrophy in systemic light chain amyloidosis: Case report
por: Draghici, Mirela, et al.
Publicado: (2021) -
Clinical characteristics in patients with hereditary amyloidosis with Glu54Gln transthyretin identified in the Romanian population
por: Jercan, Andreea, et al.
Publicado: (2020) -
Current Challenges of Cardiac Amyloidosis Awareness among Romanian Cardiologists
por: Adam, Robert, et al.
Publicado: (2021) -
Severe Aortic Stenosis and ATTRwt Amyloidosis – Beware in the Aging: A Case Report and Review of the Literature
por: Adam, Robert, et al.
Publicado: (2020) -
Quantitative SPECT/CT Parameters in the Assessment of Transthyretin Cardiac Amyloidosis—A New Dimension of Molecular Imaging
por: Gherghe, Mirela, et al.
Publicado: (2023)