Ecallantide is a novel treatment for attacks of hereditary angioedema due to C1 inhibitor deficiency
Henriette Farkas, Lilian Varga3rd Department of Internal Medicine, Semmelweis University, Budapest, HungaryAbstract: Hereditary angioedema (HAE) resulting from the deficiency of the C1 inhibitor protein is a rare disease, characterized by paroxysms of edema formation in the subcutis and in the submu...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Dove Medical Press,
2011-05-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |