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Denise Ponard

Showing results (1-10 of 24) with videos related to

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Presse Medicale (Paris, France : 1983)|December 17, 2014
[Hereditary angioedema biological diagnosis]Denise Ponard
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|December 3, 2014
Benefits of hydroxychloroquine in the treatment of a patient with angioedema due to acquired C1 inhibitor deficiencyDenis Vincent, Denise Ponard, Sandrine Fiorella, et al.
Molecular Immunology|February 22, 2017
Hereditary C1 inhibitor deficiency is associated with high spontaneous amidase activityDelphine Charignon, Arije Ghannam, Denise Ponard, et al.
The American Journal of Medicine|October 14, 2003
Clinical and biological distinctions between type I and type II acquired angioedemaLaurence Bouillet-Claveyrolas, Denise Ponard, Christian Drouet, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 7, 2018
Angioedema: Systemic activation process during prodromesSamuel Luyasu, Delphine Charignon, Denise Ponard, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|June 10, 2018
SERPING1 and F12 combined variants in a hereditary angioedema familyDelphine Charignon, Denise Ponard, Christian de Gennes, et al.
Molecular Immunology|February 22, 2016
C1 Inhibitor as a glycoprotein: The influence of polysaccharides on its function and autoantibody targetArije Ghannam, Pauline Sellier, Olivier Fain, et al.
Acta Dermato-Venereologica|June 22, 2011
Acquired angioedema responding to rituximabAmr Hassan, Stéphanie Amarger, Arlette Tridon, et al.
Molecular Immunology|March 15, 2006
Characterisation of a new C1 inhibitor mutant in a patient with hepatocellular carcinomaNicole Monnier, Denise Ponard, Christiane Duponchel, et al.
Journal of the American Society of Nephrology : JASN|May 8, 2016
Phospholipase A2 Receptor-Related Membranous Nephropathy and Mannan-Binding Lectin DeficiencyStéphane Bally, Hanna Debiec, Denise Ponard, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Presse Medicale (Paris, France : 1983)|December 17, 2014
[Hereditary angioedema biological diagnosis]Denise Ponard
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|December 3, 2014
Benefits of hydroxychloroquine in the treatment of a patient with angioedema due to acquired C1 inhibitor deficiencyDenis Vincent, Denise Ponard, Sandrine Fiorella, et al.
Molecular Immunology|February 22, 2017
Hereditary C1 inhibitor deficiency is associated with high spontaneous amidase activityDelphine Charignon, Arije Ghannam, Denise Ponard, et al.
The American Journal of Medicine|October 14, 2003
Clinical and biological distinctions between type I and type II acquired angioedemaLaurence Bouillet-Claveyrolas, Denise Ponard, Christian Drouet, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 7, 2018
Angioedema: Systemic activation process during prodromesSamuel Luyasu, Delphine Charignon, Denise Ponard, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|June 10, 2018
SERPING1 and F12 combined variants in a hereditary angioedema familyDelphine Charignon, Denise Ponard, Christian de Gennes, et al.
Molecular Immunology|February 22, 2016
C1 Inhibitor as a glycoprotein: The influence of polysaccharides on its function and autoantibody targetArije Ghannam, Pauline Sellier, Olivier Fain, et al.
Acta Dermato-Venereologica|June 22, 2011
Acquired angioedema responding to rituximabAmr Hassan, Stéphanie Amarger, Arlette Tridon, et al.
Molecular Immunology|March 15, 2006
Characterisation of a new C1 inhibitor mutant in a patient with hepatocellular carcinomaNicole Monnier, Denise Ponard, Christiane Duponchel, et al.
Journal of the American Society of Nephrology : JASN|May 8, 2016
Phospholipase A2 Receptor-Related Membranous Nephropathy and Mannan-Binding Lectin DeficiencyStéphane Bally, Hanna Debiec, Denise Ponard, et al.
Pageof 3