Blindness, tetraspasticity, and other signs of irreversible brain damage in hereditary angioedema
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology
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3. Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to c1 esterase inhibitor deficiency;Bork;Arch Intern Med,2003
4. Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency;Bork;J Allergy Clin Immunol,2012
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1. Assessing the impact of a rare synonymous variant in the <i>KNG1</i> gene on the development of hereditary angioedema;Medical Immunology (Russia);2023-11-30
2. Hereditary angioedema;Nursing;2022-12
3. Applying bioinformatic analysis for prognostic assessment of the <i>HS3ST6</i> missense mutations clinical significance in the development of hereditary angioedema;Medical Immunology (Russia);2022-11-18
4. Preventive Treatment of Hereditary Angioedema: A Review of Phase III Clinical Trial Data for Subcutaneous C1 Inhibitor and Relevance for Patient Management;Clinical Therapeutics;2021-12
5. The importance of recognizing and managing a rare form of angioedema: hereditary angioedema due to C1-inhibitor deficiency;Postgraduate Medicine;2021-05-17
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