Therapeutic options for patients with angioedema due to C1-inhibitor deficiencies: from pathophysiology to the clinic
Author:
Publisher
Informa UK Limited
Subject
Pharmacology,Toxicology,General Medicine,Immunology,Immunology and Allergy
Link
http://www.tandfonline.com/doi/pdf/10.3109/08923973.2012.726627
Reference84 articles.
1. Hereditary angio-oedema
2. Complement disorders and hereditary angioedema
3. C1-inhibitor deficiency and angioedema: molecular mechanisms and clinical progress
4. Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond
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3. Streptococcus pyogenes Endopeptidase O Contributes to Evasion from Complement-mediated Bacteriolysis via Binding to Human Complement Factor C1q;Journal of Biological Chemistry;2017-03
4. Acquired C1-inhibitor deficiency and lymphoproliferative disorders: A tight relationship;Critical Reviews in Oncology/Hematology;2013-09
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