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- W313651475 abstract "BackgroundIn hereditary angioedema (HAE), diverse mutations in the C1-inhibitor gene may produce either normal C1-inhibitor protein in insufficient quantities (HAE type I), or a dysfunctional protein in normal or even excessive amounts (HAE type II). Previously, we have found strong association between baseline level of functional C1-inhibitor and severity of HAE. Our aim was to investigate complement activation products in HAE, during a follow-up period, and to analyze the relationship between these products and severity of disease." @default.
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- W313651475 date "2012-02-01" @default.
- W313651475 modified "2023-09-27" @default.
- W313651475 title "458 Differences of Complement Activation Profile between Type I and Type II of Hereditary Angioedema Due to C1-inhibitor Deficiency" @default.
- W313651475 doi "https://doi.org/10.1097/01.wox.0000411573.74196.57" @default.
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