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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...
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| Yayımlandı: | Hemasphere |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Health
2020
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| Konular: | |
| Online Erişim: | 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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