New treatments addressing the pathophysiology of hereditary angioedema
Author:
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Immunology,Immunology and Allergy
Link
http://link.springer.com/content/pdf/10.1186/1476-7961-6-2.pdf
Reference55 articles.
1. Agostoni A, Aygoren-Pursun E, Binkley KE, Blanch A, Bork K, Bouillet L, Bucher C, Castaldo AJ, Cicardi M, Davis AE III, et al.: Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J Allergy Clin Immunol. 2004, 114: S51-131. 10.1016/j.jaci.2004.06.047
2. Davis AE III: Mechanism of angioedema in first complement component inhibitor deficiency. Immunol Allergy Clin North America. 2006, 26: 633-651. 10.1016/j.iac.2006.08.003.
3. Fay A, Abinun M: Current management of hereditary angio-oedema (C'1 esterase inhibitor deficiency). J Clin Pathol. 2002, 55: 266-270.
4. C1 inhibitor gene mutation database. http://hae.enzim.hu/
5. Bork K, Barnstedt S-E: Treatment of 193 episodes of laryngeal edema with C1-inhibitor concentrate in patients with hereditary angioedema. Arch Intern Med. 2001, 161: 714-718. 10.1001/archinte.161.5.714
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