International consensus on the use of genetics in the management of hereditary angioedema

AE Germenis, M Margaglione, JB Pesquero… - The Journal of Allergy …, 2020 - Elsevier
Hereditary angioedema (HAE) is becoming much more genetically complex than was
initially considered. Thus, the role of HAE genetics is expanding beyond research …

[HTML][HTML] Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies

V Wahn, W Aberer, W Eberl, M Faßhauer… - European journal of …, 2012 - Springer
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II
HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with …

[HTML][HTML] Canadian hereditary angioedema guideline

S Betschel, J Badiou, K Binkley, J Hébert… - Allergy, Asthma & …, 2014 - Springer
Hereditary angioedema (HAE) is a disease which is associated with random and often
unpredictable attacks of painful swelling typically affecting the extremities, bowel mucosa …

Recombinant human C1-inhibitor for the treatment of acute angioedema attacks in patients with hereditary angioedema

B Zuraw, M Cicardi, RJ Levy, JH Nuijens… - Journal of allergy and …, 2010 - Elsevier
BACKGROUND: Hereditary angioedema (HAE) results from a genetic deficiency of C1-
inhibitor. Two similar independent, randomized, saline controlled, double-blind studies were …