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Long-term use and remission of granulomatosis with polyangiitis with the oral C5a receptor inhibitor avacopan
Granulomatosis with polyangiitis (GPA) is a rare antineutrophil cytoplasm antibody-associated vasculitis. Several therapeutic advances have occurred over the past two decades, but relapse rate remains high and refractory cases are not uncommon. Here, we present the case of a female patient diagnosed...
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| Vydáno v: | BMJ Case Rep |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7597477/ https://ncbi.nlm.nih.gov/pubmed/33122227 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-236236 |
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