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Immunoglobulin Light-Chain Amyloidosis: Clinical Presentations and Diagnostic Approach
Systemic immunoglobulin light-chain (AL) amyloidosis is a rare disorder arising from a plasma cell clone that produces misfolded immunoglobulin light chains, which are deposited in various tissues and organs as amyloid fibrils. Signs and symptoms are typically vague and overlap with those arising fr...
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| Publicado no: | J Adv Pract Oncol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Harborside Press LLC
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7779572/ https://ncbi.nlm.nih.gov/pubmed/33457060 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6004/jadpro.2019.10.5.5 |
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