Cargando…
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...
| Autores principales: | , |
|---|---|
| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887436/ https://www.ncbi.nlm.nih.gov/pubmed/20497583 http://dx.doi.org/10.1186/1710-1492-6-11 |