Hereditary Angioedema
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-05147-1_10
Reference46 articles.
1. Agostoni A, Cicardi M. Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients. Medicine (Baltimore). 1992;71(4):206–15.
2. Betschel S, Badiou J, Binkley K, Hébert J, Kanani A, Keith P, et al. Canadian hereditary angioedema guideline. Allergy Asthma Clin Immunol. 2014;10(1):50. https://doi.org/10.1186/1710-1492-10-50 .
3. Bonnaud I, Rouaud V, Guyot M, Debiais S, Saudeau D, de Toffol B, et al. Exceptional stroke-like episodes in a patient with type I autosomal angioedema. Neurology. 2012;78(8):598–9. https://doi.org/10.1212/WNL.0b013e318247ca58 .
4. Bork K, Fischer B, Dewald G. Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy. Am J Med. 2003a;114(4):294–8.
5. Bork K, Hardt J, Schicketanz KH, Ressel N. Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency. Arch Intern Med. 2003b;163(10):1229–35. https://doi.org/10.1001/archinte.163.10.1229 .
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