rhC1INH: a new drug for the treatment of attacks in hereditary angioedema caused by C1-inhibitor deficiency
Author:
Publisher
Informa UK Limited
Subject
Immunology,Immunology and Allergy
Link
http://www.tandfonline.com/doi/pdf/10.1586/eci.11.5
Reference70 articles.
1. Treatment of type I and II hereditary angioedema with Rhucin®, a recombinant human C1 inhibitor
2. A biochemical abnormality in hereditary angioneurotic edema
3. Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: Functional and structural correlates
4. Diagnosis and treatment of hereditary angioedema with normal C1 inhibitor
5. Acquired angioedema
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