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Christian Drouet

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Clinical and Diagnostic Laboratory Immunology|September 11, 2003
Detection of antiendothelial cell antibodies by an enzyme-linked immunosorbent assay using antigens from cell lysate: minimal interference with antinuclear antibodies and rheumatoid factorsChristian Drouet, Marie-France Nissou, Denise Ponard, et al.
Dermatology (Basel, Switzerland)|February 28, 2015
Distinct conditions support a novel classification for bradykinin-mediated angio-oedemaPanteha Dessart, Federica Defendi, Hélène Humeau, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|November 28, 2018
The diagnosis of hereditary angioedema with C1 inhibitor deficiency: a survey of Canadian physicians and laboratoriesXavier Charest-Morin, Stephen Betschel, Rozita Borici-Mazi, et al.
Transfusion|March 26, 2019
Hypersensitivity transfusion reactions to platelet concentrate: a retrospective analysis of the French hemovigilance networkPaul M Mertes, Charles Tacquard, Georges Andreu, et al.
The Journal of Allergy and Clinical Immunology. Global|March 6, 2024
Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiencyDenis Vincent, Faidra Parsopoulou, Ludovic Martin, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 20, 2008
Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cellsArije Ghannam, Martine Pernollet, Jean-Luc Fauquert, et al.
Journal of Clinical Medicine|December 9, 2023
Recessive <i>SERPING1</i> Variant Leads to Kinin-Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary AngioedemaLuana Sella Motta Maia, Bettina Burger, Arije Ghannam, et al.
Human Mutation|September 14, 2019
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypesDenise Ponard, Christine Gaboriaud, Delphine Charignon, et al.
American Journal of Human Genetics|December 23, 2006
Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type IIISven Cichon, Ludovic Martin, Hans Christian Hennies, et al.
Plos One|August 14, 2013
Enzymatic assays for the diagnosis of bradykinin-dependent angioedemaFederica Defendi, Delphine Charignon, Arije Ghannam, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Clinical and Diagnostic Laboratory Immunology|September 11, 2003
Detection of antiendothelial cell antibodies by an enzyme-linked immunosorbent assay using antigens from cell lysate: minimal interference with antinuclear antibodies and rheumatoid factorsChristian Drouet, Marie-France Nissou, Denise Ponard, et al.
Dermatology (Basel, Switzerland)|February 28, 2015
Distinct conditions support a novel classification for bradykinin-mediated angio-oedemaPanteha Dessart, Federica Defendi, Hélène Humeau, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|November 28, 2018
The diagnosis of hereditary angioedema with C1 inhibitor deficiency: a survey of Canadian physicians and laboratoriesXavier Charest-Morin, Stephen Betschel, Rozita Borici-Mazi, et al.
Transfusion|March 26, 2019
Hypersensitivity transfusion reactions to platelet concentrate: a retrospective analysis of the French hemovigilance networkPaul M Mertes, Charles Tacquard, Georges Andreu, et al.
The Journal of Allergy and Clinical Immunology. Global|March 6, 2024
Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiencyDenis Vincent, Faidra Parsopoulou, Ludovic Martin, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 20, 2008
Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cellsArije Ghannam, Martine Pernollet, Jean-Luc Fauquert, et al.
Journal of Clinical Medicine|December 9, 2023
Recessive <i>SERPING1</i> Variant Leads to Kinin-Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary AngioedemaLuana Sella Motta Maia, Bettina Burger, Arije Ghannam, et al.
Human Mutation|September 14, 2019
SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypesDenise Ponard, Christine Gaboriaud, Delphine Charignon, et al.
American Journal of Human Genetics|December 23, 2006
Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type IIISven Cichon, Ludovic Martin, Hans Christian Hennies, et al.
Plos One|August 14, 2013
Enzymatic assays for the diagnosis of bradykinin-dependent angioedemaFederica Defendi, Delphine Charignon, Arije Ghannam, et al.
Pageof 5