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Alain Fischer

Showing results (461-470 of 493) with videos related to

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Blood|July 14, 2012
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiencyAmel Hassan, Claire Booth, Alex Brightwell, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2016
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort studyElodie Elkaim, Benedicte Neven, Julie Bruneau, et al.
The Journal of Allergy and Clinical Immunology|September 24, 2016
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysisCarsten Speckmann, Sam Doerken, Alessandro Aiuti, et al.
The Journal of Allergy and Clinical Immunology. in Practice|June 26, 2025
Clinical and Molecular Characteristics of X-Linked Agammaglobulinemia Patients 55 Years or OlderAaron T Chin, Hans D Ochs, Roger Kobayashi, et al.
Blood|January 31, 2022
Hematopoietic stem cell transplantation for Wiskott-Aldrich syndrome: an EBMT Inborn Errors Working Party analysisMichael H Albert, Mary A Slatter, Andrew R Gennery, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2018
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated <i>RPSA</i> exonsAlexandre Bolze, Bertrand Boisson, Barbara Bosch, et al.
The Journal of Allergy and Clinical Immunology|June 13, 2020
Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencingMathieu Fusaro, Jérémie Rosain, Virginie Grandin, et al.
Nature Genetics|November 16, 2018
Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndromeTenzin Gayden, Fernando E Sepulveda, Dong-Anh Khuong-Quang, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Science (New York, N.Y.)|October 19, 2013
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damageIvan Angulo, Oscar Vadas, Fabien Garçon, et al.
Pageof 50

Showing results (461-470 of 493) with videos related to

Sort By:
Pageof 50
Blood|July 14, 2012
Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiencyAmel Hassan, Claire Booth, Alex Brightwell, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2016
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort studyElodie Elkaim, Benedicte Neven, Julie Bruneau, et al.
The Journal of Allergy and Clinical Immunology|September 24, 2016
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysisCarsten Speckmann, Sam Doerken, Alessandro Aiuti, et al.
The Journal of Allergy and Clinical Immunology. in Practice|June 26, 2025
Clinical and Molecular Characteristics of X-Linked Agammaglobulinemia Patients 55 Years or OlderAaron T Chin, Hans D Ochs, Roger Kobayashi, et al.
Blood|January 31, 2022
Hematopoietic stem cell transplantation for Wiskott-Aldrich syndrome: an EBMT Inborn Errors Working Party analysisMichael H Albert, Mary A Slatter, Andrew R Gennery, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2018
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated <i>RPSA</i> exonsAlexandre Bolze, Bertrand Boisson, Barbara Bosch, et al.
The Journal of Allergy and Clinical Immunology|June 13, 2020
Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencingMathieu Fusaro, Jérémie Rosain, Virginie Grandin, et al.
Nature Genetics|November 16, 2018
Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndromeTenzin Gayden, Fernando E Sepulveda, Dong-Anh Khuong-Quang, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Science (New York, N.Y.)|October 19, 2013
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damageIvan Angulo, Oscar Vadas, Fabien Garçon, et al.
Pageof 50