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Alain Fischer

Showing results (441-450 of 493) with videos related to

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Journal of Human Immunity|December 5, 2025
Inborn errors of immunity: Manifestation, treatment, and outcome-an ESID registry 1994-2024 report on 30,628 patientsGerhard Kindle, Mickaël Alligon, Michael H Albert, et al.
The Journal of Clinical Investigation|December 8, 2020
Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiencyBethany A Pillay, Mathieu Fusaro, Paul E Gray, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
Blood|July 18, 2015
Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow TransplantationFrancesca Fioredda, Simona Iacobelli, Anja van Biezen, et al.
Blood|April 4, 2019
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genesJérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes, et al.
Journal of Clinical Immunology|November 5, 2025
Consecutive non-Aspergillus Fungal Invasive Infections in Chronic Granulomatous Disease: Data from the French National Reference Center for Primary ImmunoDeficiencies and literature reviewLeïla Lefevre, Olivier Paccoud, Bénédicte Neven, et al.
The Journal of Allergy and Clinical Immunology|October 4, 2023
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndromeOlivier Pellé, Solange Moreno, Myriam Ricarda Lorenz, et al.
Blood|December 2, 2010
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
Pageof 50

Showing results (441-450 of 493) with videos related to

Sort By:
Pageof 50
Journal of Human Immunity|December 5, 2025
Inborn errors of immunity: Manifestation, treatment, and outcome-an ESID registry 1994-2024 report on 30,628 patientsGerhard Kindle, Mickaël Alligon, Michael H Albert, et al.
The Journal of Clinical Investigation|December 8, 2020
Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiencyBethany A Pillay, Mathieu Fusaro, Paul E Gray, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
Blood|July 18, 2015
Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow TransplantationFrancesca Fioredda, Simona Iacobelli, Anja van Biezen, et al.
Blood|April 4, 2019
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genesJérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes, et al.
Journal of Clinical Immunology|November 5, 2025
Consecutive non-Aspergillus Fungal Invasive Infections in Chronic Granulomatous Disease: Data from the French National Reference Center for Primary ImmunoDeficiencies and literature reviewLeïla Lefevre, Olivier Paccoud, Bénédicte Neven, et al.
The Journal of Allergy and Clinical Immunology|October 4, 2023
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndromeOlivier Pellé, Solange Moreno, Myriam Ricarda Lorenz, et al.
Blood|December 2, 2010
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
Pageof 50