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Capucine Picard

Showing results (241-250 of 400) with videos related to

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Journal of Clinical Immunology|June 24, 2022
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert CommitteeStuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.
Journal of Human Immunity|January 29, 2026
The 2024 update of IUIS phenotypic classification of human inborn errors of immunityAhmed Aziz Bousfiha, Leïla Jeddane, Abderrahmane Moundir, et al.
Blood Advances|January 27, 2019
Successful in utero stem cell transplantation in X-linked severe combined immunodeficiencyAlessandra Magnani, Jean-Marie Jouannic, Jérémie Rosain, et al.
Orphanet Journal of Rare Diseases|December 11, 2014
Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia RegistryClaire Desplantes, Marie Louise Fremond, Blandine Beaupain, et al.
Journal of Clinical Immunology|February 13, 2020
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical ClassificationAziz Bousfiha, Leila Jeddane, Capucine Picard, et al.
The Journal of Allergy and Clinical Immunology|September 2, 2014
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiencyRoxane Lemoine, Jana Pachlopnik-Schmid, Henner F Farin, et al.
Blood|September 3, 2011
A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutationBénédicte Neven, Aude Magerus-Chatinet, Benoit Florkin, et al.
The Journal of Allergy and Clinical Immunology|January 18, 2025
Curation of gene-disease relationships in primary antibody deficiencies using the ClinGen validation frameworkAlejandro Nieto-Patlán, Justyne Ross, Shruthi Mohan, et al.
Journal of Clinical Immunology|February 3, 2021
Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and MalformationsMathieu Fusaro, Aline Vincent, Martin Castelle, et al.
Science Immunology|March 25, 2022
Gain-of-function <i>IKZF1</i> variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiationAkihiro Hoshino, David Boutboul, Yuan Zhang, et al.
Pageof 40

Showing results (241-250 of 400) with videos related to

Sort By:
Pageof 40
Journal of Clinical Immunology|June 24, 2022
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert CommitteeStuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.
Journal of Human Immunity|January 29, 2026
The 2024 update of IUIS phenotypic classification of human inborn errors of immunityAhmed Aziz Bousfiha, Leïla Jeddane, Abderrahmane Moundir, et al.
Blood Advances|January 27, 2019
Successful in utero stem cell transplantation in X-linked severe combined immunodeficiencyAlessandra Magnani, Jean-Marie Jouannic, Jérémie Rosain, et al.
Orphanet Journal of Rare Diseases|December 11, 2014
Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia RegistryClaire Desplantes, Marie Louise Fremond, Blandine Beaupain, et al.
Journal of Clinical Immunology|February 13, 2020
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical ClassificationAziz Bousfiha, Leila Jeddane, Capucine Picard, et al.
The Journal of Allergy and Clinical Immunology|September 2, 2014
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiencyRoxane Lemoine, Jana Pachlopnik-Schmid, Henner F Farin, et al.
Blood|September 3, 2011
A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutationBénédicte Neven, Aude Magerus-Chatinet, Benoit Florkin, et al.
The Journal of Allergy and Clinical Immunology|January 18, 2025
Curation of gene-disease relationships in primary antibody deficiencies using the ClinGen validation frameworkAlejandro Nieto-Patlán, Justyne Ross, Shruthi Mohan, et al.
Journal of Clinical Immunology|February 3, 2021
Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and MalformationsMathieu Fusaro, Aline Vincent, Martin Castelle, et al.
Science Immunology|March 25, 2022
Gain-of-function <i>IKZF1</i> variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiationAkihiro Hoshino, David Boutboul, Yuan Zhang, et al.
Pageof 40