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Published in 2018 at "Pediatrics"
DOI: 10.1542/peds.142.1_meetingabstract.812
Abstract: Background: Hereditary angioedema (HAE), caused by absolute or functional deficiency of C1-esterase inhibitor (C1-INH), is characterized by recurrent, disfiguring, and potentially life-threatening attacks of subcutaneous and submucosal edema. The mean age of first attack is…
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Keywords:
phase trial;
hereditary angioedema;
inhibitor inh;
esterase inhibitor ... See more keywords