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Published in 2019 at "International immunopharmacology"
DOI: 10.1016/j.intimp.2019.106079
Abstract: Hereditary angioedema is a disabling, life-threatening condition caused by deficiency (type I) or dysfunction (type II) of the C1 inhibitor protein (C1-INH-HAE) leading to bradykinin accumulation and recurrent episodes of edema attack. Vascular leakage is…
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Keywords:
attack;
remission;
vasoactive mediators;
patients inh ... See more keywords