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Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
AL amyloidosis is characterized by a low-level expansion of an indolent, small plasma cell clone that produces amyloidogenic light chains. Amyloid aggregates or preceding intermediaries cause direct cell damage through their proteotoxicity, and amyloid deposits distort tissue architecture, and, even...
Gorde:
| Argitaratua izan da: | Hemasphere |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Wolters Kluwer Health
2020
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7430233/ https://ncbi.nlm.nih.gov/pubmed/32885146 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/HS9.0000000000000454 |
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