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Arnon Broides

Showing results (51-60 of 63) with videos related to

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Journal of Clinical Immunology|December 6, 2022
SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related LymphomaAtar Lev, Mahdi Asleh, Shiran Levy, et al.
The Journal of Allergy and Clinical Immunology|November 29, 2019
Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiencyAmit Nahum, Nigel Sharfe, Arnon Broides, et al.
Immunologic Research|January 11, 2017
The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutationArnon Broides, Amarilla B Mandola, Jacov Levy, et al.
Frontiers in Immunology|August 6, 2019
Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With <i>IL7RA</i> MutationAtar Lev, Amos J Simon, Ortal Barel, et al.
Frontiers in Immunology|November 24, 2017
First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and InsightsErez Rechavi, Atar Lev, Amos J Simon, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 29, 2022
Lessons Learned From Five Years of Newborn Screening for Severe Combined Immunodeficiency in IsraelAtar Lev, Idan Sharir, Amos J Simon, et al.
American Journal of Hematology|October 5, 2016
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Blood|September 22, 2023
Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signalingRuth Shiloh, Ruth Lubin, Odeya David, et al.
Blood|June 21, 2024
Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohortBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
Human Mutation|July 19, 2013
IL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation databaseEsther van de Vosse, Margje H Haverkamp, Noe Ramirez-Alejo, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Journal of Clinical Immunology|December 6, 2022
SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related LymphomaAtar Lev, Mahdi Asleh, Shiran Levy, et al.
The Journal of Allergy and Clinical Immunology|November 29, 2019
Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiencyAmit Nahum, Nigel Sharfe, Arnon Broides, et al.
Immunologic Research|January 11, 2017
The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutationArnon Broides, Amarilla B Mandola, Jacov Levy, et al.
Frontiers in Immunology|August 6, 2019
Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With <i>IL7RA</i> MutationAtar Lev, Amos J Simon, Ortal Barel, et al.
Frontiers in Immunology|November 24, 2017
First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and InsightsErez Rechavi, Atar Lev, Amos J Simon, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 29, 2022
Lessons Learned From Five Years of Newborn Screening for Severe Combined Immunodeficiency in IsraelAtar Lev, Idan Sharir, Amos J Simon, et al.
American Journal of Hematology|October 5, 2016
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Blood|September 22, 2023
Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signalingRuth Shiloh, Ruth Lubin, Odeya David, et al.
Blood|June 21, 2024
Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohortBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
Human Mutation|July 19, 2013
IL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation databaseEsther van de Vosse, Margje H Haverkamp, Noe Ramirez-Alejo, et al.
Pageof 7