Flow-mediated vasodilation assay indicates no endothelial dysfunction in hereditary angioedema patients with C1-inhibitor deficiency
Author:
Funder
Hungarian Scientific Research Fund
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology
Reference39 articles.
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3. New topics in bradykinin research;Maurer;Allergy Eur J Allergy Clin. Immunol.,2011
4. Endothelial cell function in patients with hereditary angioedema: elevated soluble E-selectin level during inter-attack periods;Czúcz;J Clin Immunol,2012
5. Hereditary angioedema: key role for kallikrein and bradykinin in vascular endothelial-cadherin cleavage and edema formation;Bouillet;J Allergy Clin Immunol,2011
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2. Transition to lanadelumab‐flyo from three medications for a hereditary angioedema patient with a variant in the SYTL2 gene: A case report;Clinical Case Reports;2021-03-20
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4. The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiency;International Immunopharmacology;2020-05
5. Is hereditary angioedema related to an increased risk of atherosclerosis?;Annals of Allergy, Asthma & Immunology;2019-02
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