Human recombinant interferon alfa-2a for the treatment of Behçet's disease with sight threatening posterior or panuveitis

Background: Behçet's disease is a multisystem vasculitis of unknown origin. Standard treatment mainly comprises systemic immunosuppressive agents. Ocular involvement, mostly posterior uveitis with retinal vasculitis, leads to blindness in 20–50% of the involved eyes within 5 years. The efficacy...

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Main Authors: Kötter, I, Zierhut, M, Eckstein, A K, Vonthein, R, Ness, T, Günaydin, I, Grimbacher, B, Blaschke, S, Meyer-Riemann, W, Peter, H H, Stübiger, N
Formáid: Artigo
Teanga:Inglês
Foilsithe: Copyright 2003 British Journal of Ophthalmology 2003
Ábhair:
Clinical Science
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1771623/
https://ncbi.nlm.nih.gov/pubmed/12642304
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