C1 inhibitor deficiency: consensus document

We present a consensus document on the diagnosis and management of C1 inhibitor deficiency, a syndrome characterized clinically by recurrent episodes of angio-oedema. In hereditary angio-oedema, a rare autosomal dominant condition, C1 inhibitor function is reduced due to impaired transcription or pr...

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Detalhes bibliográficos
Main Authors: Gompels, M M, Lock, R J, Abinun, M, Bethune, C A, Davies, G, Grattan, C, Fay, A C, Longhurst, H J, Morrison, L, Price, A, Price, M, Watters, D
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2005
Assuntos:
Review
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1809312/
https://ncbi.nlm.nih.gov/pubmed/15730382
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2249.2005.02726.x
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