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Atypical hemolytic uremic syndrome: a syndrome in need of clarity
Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA) originally understood to be limited to renal and hematopoietic involvement. Whereas aberrations in complement regulatory proteins (CRPs), C3 or complement factor B (CFB) are detected in ∼60% of patients, a complement-der...
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| Udgivet i: | Clin Kidney J |
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| Hovedforfatter: | |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6543964/ https://ncbi.nlm.nih.gov/pubmed/31198222 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfy066 |
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