Delphine Charignon
Grenoble, France
Last Updated: 09/26/2026
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Found 13 publications
Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients.
Journal: Allergy
Published: January 16, 2020
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes.
Journal: Human mutation
Published: April 02, 2019
SERPING1 and F12 combined variants in a hereditary angioedema family.
Journal: Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
Published: March 19, 2018
Angioedema: Systemic activation process during prodromes.
Journal: Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
Published: February 12, 2018
Hereditary C1 inhibitor deficiency is associated with high spontaneous amidase activity.
Journal: Molecular immunology
Published: December 22, 2016
Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions.
Journal: PloS one
Published: May 27, 2016
C1 inhibitor function using contact-phase proteases as target: evaluation of an innovative assay.
Journal: Allergy
Published: May 20, 2015
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
Journal: Allergy
Published: August 12, 2014
Biological investigation of kinin-mediated angioedema
Journal: Annales de dermatologie et de venereologie
Published: June 25, 2014
Distinct conditions support a novel classification for bradykinin-mediated angio-oedema.
Journal: Dermatology (Basel, Switzerland)
Published: May 13, 2014
Contact system activation in patients with HAE and normal C1 inhibitor function.
Journal: Immunology and allergy clinics of North America
Published: November 02, 2013
Enzymatic assays for the diagnosis of bradykinin-dependent angioedema.
Journal: PloS one
Published: May 14, 2013
Last Updated: 09/26/2026