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Recombinant Human C1 Esterase Inhibitor in the Management of Hereditary Angioedema
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency in functional C1 esterase inhibitor (C1-INH). This potentially life-threatening condition manifests as recurrent attacks of subcutaneous and submucosal swelling of the skin, gastrointestinal tract and...
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| Gepubliceerd in: | Clin Drug Investig |
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| Hoofdauteur: | |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Springer International Publishing
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4488495/ https://ncbi.nlm.nih.gov/pubmed/26091744 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40261-015-0300-z |
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