Factor XII mutations, estrogen-dependent inherited angioedema, and related conditions
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine,Immunology,Immunology and Allergy
Link
http://link.springer.com/content/pdf/10.1186/1710-1492-6-16.pdf
Reference49 articles.
1. Binkley KE, Davis A: Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema. J Allergy Clin Immunol. 2000, 106: 546-50. 10.1067/mai.2000.108106.
2. Bork K, Barnstedt SE, Koch P, Traupe H: Hereditary angioedema with normal C1-inhibitor activity in women. Lancet. 2000, 356: 213-7. 10.1016/S0140-6736(00)02483-1.
3. Martin L, Degenene D, Toutain A, Ponard D, Watier H: Hereditary angioedema type III: an additional French pedigree with autosomal dominant transmission. J Allergy Clin Immunol. 2001, 107: 747-8. 10.1067/mai.2001.114242.
4. Herrmann G, Schneider L, Krieg T, Hunzelmann N, Scharfetter-Kochanek K: Efficacy of danazol treatment in a patient with a new variant of hereditary angiooedema (HAE III). Br J Dermatol. 2004, 150: 157-8. 10.1111/j.1365-2133.2004.05669.x.
5. Bouillet L, Ponard D, Rousset H, Cichon S, Drouet C: A case of hereditary angioedema type III presenting with C1-inhibitor cleavage and a missense mutation in the F12 gene. Br J Dermatol. 2007, 156: 1063-5. 10.1111/j.1365-2133.2007.07778.x.
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