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Treatment of Hereditary Angioedema: items that need to be addressed in practice parameter
BACKGROUND: Hereditary Angioedema (HAE) is a rare, autosomal dominant (AD) disorder caused by a C1 esterase inhibitor (C1-inh) deficiency or qualitative defect. Treatment of HAE in many parts of the world fall short and certain items need to be addressed in future guidelines. OBJECTIVE: To identify...
Bewaard in:
| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2887436/ https://ncbi.nlm.nih.gov/pubmed/20497583 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1710-1492-6-11 |
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