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Anti-interleukin 6 receptor therapy for hyper-IgD syndrome
Hyper-IgD syndrome (HIDS) is a rare, severe hereditary autoinflammatory disease characterised by periodic fevers, elevated serum IgD levels and a wide range of symptoms. Although a few randomised controlled trials have been performed in this disorder, there are no straightforward treatment protocols...
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| Publicado no: | BMJ Case Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4636692/ https://ncbi.nlm.nih.gov/pubmed/26516243 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-210513 |
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