Hereditary Angioedema
Author:
Affiliation:
1. From the Division of Clinical Immunology and Allergy, Icahn School of Medicine at Mount Sinai, New York (P.J.B.); and the Department of Medicine, University of California, San Diego, San Diego (S.C.C.).
Publisher
Massachusetts Medical Society
Subject
General Medicine
Link
http://www.nejm.org/doi/pdf/10.1056/NEJMra1808012
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1. Analysis of disease burden in patients with hereditary angioedema from Japan by patient‐reported outcomes;The Journal of Dermatology;2024-09-11
2. A practical guide to recognize allergic and immunologic skin diseases: diagnosis at first sight;Exploration of Asthma & Allergy;2024-08-26
3. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency;Gene;2024-08
4. Inter-α-trypsin inhibitor heavy chain 4 (ITIH4) as a compensatory protease inhibitor in hereditary angioedema;Journal of Allergy and Clinical Immunology;2024-08
5. Contact System Activation and Bradykinin Generation in Angioedema;Immunology and Allergy Clinics of North America;2024-08
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