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Soma Jyonouchi

Showing results (11-20 of 27) with videos related to

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Journal of Clinical Immunology|May 26, 2017
Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined ImmunodeficiencyJessica C Barry, Terrence Blaine Crowley, Soma Jyonouchi, et al.
The Journal of Allergy and Clinical Immunology. in Practice|December 3, 2014
Fiscal implications of newborn screening in the diagnosis of severe combined immunodeficiencyCatherine Kubiak, Soma Jyonouchi, Caroline Kuo, et al.
Clinical Immunology (Orlando, Fla.)|February 25, 2017
Phase I trial of low-dose interleukin 2 therapy in patients with Wiskott-Aldrich syndromeSoma Jyonouchi, Brenda Gwafila, Lavesh A Gwalani, et al.
The Journal of Allergy and Clinical Immunology. in Practice|March 14, 2017
Smith-Magenis Syndrome Patients Often Display Antibody Deficiency but Not Other Immune PathologiesTiffany Perkins, Jacob M Rosenberg, Carole Le Coz, et al.
Journal of Clinical Immunology|February 3, 2023
Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 DuplicationsDharmagat Bhattarai, Daniel E McGinn, T Blaine Crowley, et al.
The Journal of Allergy and Clinical Immunology|October 4, 2011
Autoimmune regulator (AIRE) contributes to Dectin-1-induced TNF-α production and complexes with caspase recruitment domain-containing protein 9 (CARD9), spleen tyrosine kinase (Syk), and Dectin-1Luis A Pedroza, Vipul Kumar, Keri B Sanborn, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
The Journal of Allergy and Clinical Immunology|August 25, 2019
Common variable immunodeficiency-associated endotoxemia promotes early commitment to the T follicular lineageCarole Le Coz, Bertram Bengsch, Caroline Khanna, et al.
The Journal of Allergy and Clinical Immunology|June 24, 2018
Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responsesNeil Romberg, Carole Le Coz, Salomé Glauzy, et al.
American Journal of Medical Genetics. Part A|February 8, 2014
Cornelia de Lange syndrome: further delineation of phenotype, cohesin biology and educational focus, 5th Biennial Scientific and Educational Symposium abstractsAntonie D Kline, Anne L Calof, Cheri A Schaaf, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Journal of Clinical Immunology|May 26, 2017
Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined ImmunodeficiencyJessica C Barry, Terrence Blaine Crowley, Soma Jyonouchi, et al.
The Journal of Allergy and Clinical Immunology. in Practice|December 3, 2014
Fiscal implications of newborn screening in the diagnosis of severe combined immunodeficiencyCatherine Kubiak, Soma Jyonouchi, Caroline Kuo, et al.
Clinical Immunology (Orlando, Fla.)|February 25, 2017
Phase I trial of low-dose interleukin 2 therapy in patients with Wiskott-Aldrich syndromeSoma Jyonouchi, Brenda Gwafila, Lavesh A Gwalani, et al.
The Journal of Allergy and Clinical Immunology. in Practice|March 14, 2017
Smith-Magenis Syndrome Patients Often Display Antibody Deficiency but Not Other Immune PathologiesTiffany Perkins, Jacob M Rosenberg, Carole Le Coz, et al.
Journal of Clinical Immunology|February 3, 2023
Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 DuplicationsDharmagat Bhattarai, Daniel E McGinn, T Blaine Crowley, et al.
The Journal of Allergy and Clinical Immunology|October 4, 2011
Autoimmune regulator (AIRE) contributes to Dectin-1-induced TNF-α production and complexes with caspase recruitment domain-containing protein 9 (CARD9), spleen tyrosine kinase (Syk), and Dectin-1Luis A Pedroza, Vipul Kumar, Keri B Sanborn, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
The Journal of Allergy and Clinical Immunology|August 25, 2019
Common variable immunodeficiency-associated endotoxemia promotes early commitment to the T follicular lineageCarole Le Coz, Bertram Bengsch, Caroline Khanna, et al.
The Journal of Allergy and Clinical Immunology|June 24, 2018
Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responsesNeil Romberg, Carole Le Coz, Salomé Glauzy, et al.
American Journal of Medical Genetics. Part A|February 8, 2014
Cornelia de Lange syndrome: further delineation of phenotype, cohesin biology and educational focus, 5th Biennial Scientific and Educational Symposium abstractsAntonie D Kline, Anne L Calof, Cheri A Schaaf, et al.
Pageof 3