Cargando…
Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis
Amyloidosis describes a family of related disease states associated with the extracellular tissue deposition of fibrils composed of low-molecular-weight subunits of a variety of proteins circulating as constituents of plasma. Depending on the disease subtype, fibrillar deposits in a several organs i...
Autores principales: | Puig-Carrion, Gisela D., Reyentovich, Alex, Katz, Stuart D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763576/ https://www.ncbi.nlm.nih.gov/pubmed/31452023 http://dx.doi.org/10.1007/s10286-019-00629-5 |
Ejemplares similares
-
Hereditary transthyretin amyloidosis overview
por: Manganelli, Fiore, et al.
Publicado: (2020) -
Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
por: Palma, Jose-Alberto, et al.
Publicado: (2019) -
Inotersen: new promise for the treatment of hereditary transthyretin amyloidosis
por: Mathew, Veena, et al.
Publicado: (2019) -
Advances in the treatment of hereditary transthyretin amyloidosis: A review
por: Gertz, Morie A., et al.
Publicado: (2019) -
Hereditary transthyretine amyloidosis in Slovenia
por: Zidar, Janez
Publicado: (2015)