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Capucine Picard

Showing results (261-270 of 400) with videos related to

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Journal of Clinical Immunology|October 5, 2022
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of ImmunityAziz Bousfiha, Abderrahmane Moundir, Stuart G Tangye, et al.
Human Mutation|February 24, 2009
Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndromeLoïc de Pontual, Yves Mathieu, Christelle Golzio, et al.
Gastroenterology|June 12, 2010
Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathyNicolette Moes, Frédéric Rieux-Laucat, Bernadette Begue, et al.
Elife|January 21, 2015
Phenotypic complementation of genetic immunodeficiency by chronic herpesvirus infectionDonna A MacDuff, Tiffany A Reese, Jacqueline M Kimmey, et al.
The Journal of Clinical Investigation|September 3, 2024
Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiencyMarta Benavides-Nieto, Frédéric Adam, Emmanuel Martin, et al.
The Journal of Allergy and Clinical Immunology|June 21, 2020
DEF6 deficiency, a mendelian susceptibility to EBV infection, lymphoma, and autoimmunityBenjamin Fournier, Maud Tusseau, Marine Villard, et al.
Nature Immunology|September 13, 2016
Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
The Journal of Infectious Diseases|June 30, 2026
Cryptosporidiosis in Ptients with Inborn Errors of Immunity: Retrospective cohort study of the French National Reference Center (CEREDIH)Deborah To Puzenat, Morgane Cheminant, Eric Dannaoui, et al.
Journal of Clinical Immunology|December 12, 2017
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of ImmunityCapucine Picard, H Bobby Gaspar, Waleed Al-Herz, et al.
Clinical Immunology (Orlando, Fla.)|January 14, 2018
Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutationsCaroline Besnard, Eva Levy, Nathalie Aladjidi, et al.
Pageof 40

Showing results (261-270 of 400) with videos related to

Sort By:
Pageof 40
Journal of Clinical Immunology|October 5, 2022
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of ImmunityAziz Bousfiha, Abderrahmane Moundir, Stuart G Tangye, et al.
Human Mutation|February 24, 2009
Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndromeLoïc de Pontual, Yves Mathieu, Christelle Golzio, et al.
Gastroenterology|June 12, 2010
Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathyNicolette Moes, Frédéric Rieux-Laucat, Bernadette Begue, et al.
Elife|January 21, 2015
Phenotypic complementation of genetic immunodeficiency by chronic herpesvirus infectionDonna A MacDuff, Tiffany A Reese, Jacqueline M Kimmey, et al.
The Journal of Clinical Investigation|September 3, 2024
Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiencyMarta Benavides-Nieto, Frédéric Adam, Emmanuel Martin, et al.
The Journal of Allergy and Clinical Immunology|June 21, 2020
DEF6 deficiency, a mendelian susceptibility to EBV infection, lymphoma, and autoimmunityBenjamin Fournier, Maud Tusseau, Marine Villard, et al.
Nature Immunology|September 13, 2016
Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
The Journal of Infectious Diseases|June 30, 2026
Cryptosporidiosis in Ptients with Inborn Errors of Immunity: Retrospective cohort study of the French National Reference Center (CEREDIH)Deborah To Puzenat, Morgane Cheminant, Eric Dannaoui, et al.
Journal of Clinical Immunology|December 12, 2017
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of ImmunityCapucine Picard, H Bobby Gaspar, Waleed Al-Herz, et al.
Clinical Immunology (Orlando, Fla.)|January 14, 2018
Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutationsCaroline Besnard, Eva Levy, Nathalie Aladjidi, et al.
Pageof 40