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• W2028803931 startingPage "457" @default.
• W2028803931 abstract "Until recently it was assumed that hereditary angioedema was a disease that results exclusively from a genetic deficiency of the C1 inhibitor. In 2000, families with hereditary angioedema, normal C1 inhibitor activity, and protein in plasma were described. Since then, numerous patients and families with that condition have been reported. Most of the patients were women. In many of the affected women, oral contraceptives, hormone replacement therapy containing estrogens, and pregnancies triggered the clinical symptoms. In some families mutations in the coagulation factor XII (Hageman factor) gene were detected." @default.
• W2028803931 created "2016-06-24" @default.
• W2028803931 creator A5088431125 @default.
• W2028803931 date "2013-11-01" @default.
• W2028803931 modified "2023-10-02" @default.
• W2028803931 title "Hereditary Angioedema with Normal C1 Inhibitor" @default.
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• W2028803931 doi "https://doi.org/10.1016/j.iac.2013.07.002" @default.
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