Nalaganje...
The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency
Hereditary angioedema (HAE) is a rare condition, mostly due to genetic deficiency of complement C1 inhibitor (C1-INH). The rarity of HAE impedes extensive data collection and assessment of the impact of certain factors known to affect the course of this disabling and life-threatening disease. Establ...
Shranjeno v:
| izdano v: | Clin Rev Allergy Immunol |
|---|---|
| Main Authors: | , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer US
2021
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8282542/ https://ncbi.nlm.nih.gov/pubmed/33791951 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12016-021-08855-4 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|