Factor VII activating protease (FSAP) is not essential in the pathophysiology of angioedema in patients with C1 inhibitor deficiency

Author:

Gramstad Olav RogdeORCID,Kandanur Sai Priya Sarma,Etscheid Michael,Nielsen Erik Waage,Kanse Sandip MahadevORCID

Publisher

Elsevier BV

Subject

Molecular Biology,Immunology

Reference50 articles.

1. Blood Clotting and the Pathogenesis of Types I and II Hereditary Angioedema [published online ahead of print, 2021 May 6];de Maat;Clin. Rev. Allergy Immunol.,2021

2. Serum metabolism of bradykinin and des-Arg9-bradykinin in patients with angiotensin-converting enzyme inhibitor-associated angioedema;Blais;Immunopharmacology,1999

3. Plasminogen activator in normal subjects after exercise and venous occlusion: t-PA circulates as complexes with C1-inhibitor and PAI-1;Booth;Blood,1987

4. Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation [published online ahead of print, 2021 Jan 25];Bork;J. Allergy Clin. Immunol.,2021

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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