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Behçet’s disease: from Hippocrates to the third millennium

Behçet’s disease (BD) is characterised by recurrent episodes of orogenital aphthae, systemic vasculitis, and systemic and retinal venous thrombosis. An association between HLA-B51 and BD was first identified over 20 years ago, but recently identified gene associations implicate regions both within a...

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Detalles Bibliográficos
Main Authors: Verity, D H, Wallace, G R, Vaughan, R W, Stanford, M R
Formato: Artigo
Idioma:Inglês
Publicado: Copyright 2003 British Journal of Ophthalmology 2003
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1771837/
https://ncbi.nlm.nih.gov/pubmed/12928293
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