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Ocular Manifestations of Granulomatosis with Polyangiitis: A Review of the Literature
Granulomatosis with polyangiitis (GPA) is a rare systemic autoimmune disease of unknown etiology that is characterized by granulomatous inflammation, tissue necrosis, and vasculitis in small- and medium-sized vessels. Ocular and orbital manifestations are common in almost half of patients with GPA,...
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| Publicado no: | Ophthalmol Ther |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Healthcare
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6513923/ https://ncbi.nlm.nih.gov/pubmed/30875067 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40123-019-0176-8 |
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