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Blood
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May 21, 2021
HSCT corrects primary immunodeficiency and immune dysregulation in patients with POMP-related autoinflammatory disease
Caridad Martinez, Frédéric Ebstein, Sarah K Nicholas, et al.
The Journal of Allergy and Clinical Immunology
|
August 28, 2014
Severe cutaneous human papillomavirus infection associated with natural killer cell deficiency following stem cell transplantation for severe combined immunodeficiency
Qurat Ul Ain Kamili, Filiz O Seeborg, Kapil Saxena, et al.
Neurology
|
August 17, 1999
The effect of anti-alpha4 integrin antibody on brain lesion activity in MS. The UK Antegren Study Group
N Tubridy, P O Behan, R Capildeo, et al.
Hospital Pediatrics
|
March 3, 2022
Severe Pediatric COVID-19 Pneumonia Treated With Adjuvant Anakinra
Leigh A Stubbs, Vibha Szafron, Lisa R Forbes, et al.
The Journal of Allergy and Clinical Immunology
|
February 1, 2017
Ruxolitinib reverses dysregulated T helper cell responses and controls autoimmunity caused by a novel signal transducer and activator of transcription 1 (STAT1) gain-of-function mutation
Katja G Weinacht, Louis-Marie Charbonnier, Fayhan Alroqi, et al.
Frontiers in Pediatrics
|
August 17, 2019
Novel Heterozygous Mutation in <i>NFKB2</i> Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome
Alejandra Aird, Macarena Lagos, Alexander Vargas-Hernández, et al.
The Journal of Allergy and Clinical Immunology
|
March 28, 2016
A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism
Petra Netter, Sanny K Chan, Pinaki P Banerjee, et al.
The Journal of Allergy and Clinical Immunology
|
January 14, 2018
Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatment
Raquel Ruiz-García, Alexander Vargas-Hernández, Ivan K Chinn, et al.
Science (New York, N.Y.)
|
October 7, 2021
Conformer-specific photochemistry imaged in real space and time
E G Champenois, D M Sanchez, J Yang, et al.
The Journal of Allergy and Clinical Immunology
|
February 6, 2025
Clinical, immunologic, and genetic characteristics of 148 patients with natural killer cell deficiency
Manar Abdalgani, Evelyn R Hernandez, Luis A Pedroza, et al.
Page
of 34
Search research articles
Search
Showing results (291-300 of 339) with videos related to
Sort By:
Page
of 34
Blood
|
May 21, 2021
HSCT corrects primary immunodeficiency and immune dysregulation in patients with POMP-related autoinflammatory disease
Caridad Martinez, Frédéric Ebstein, Sarah K Nicholas, et al.
The Journal of Allergy and Clinical Immunology
|
August 28, 2014
Severe cutaneous human papillomavirus infection associated with natural killer cell deficiency following stem cell transplantation for severe combined immunodeficiency
Qurat Ul Ain Kamili, Filiz O Seeborg, Kapil Saxena, et al.
Neurology
|
August 17, 1999
The effect of anti-alpha4 integrin antibody on brain lesion activity in MS. The UK Antegren Study Group
N Tubridy, P O Behan, R Capildeo, et al.
Hospital Pediatrics
|
March 3, 2022
Severe Pediatric COVID-19 Pneumonia Treated With Adjuvant Anakinra
Leigh A Stubbs, Vibha Szafron, Lisa R Forbes, et al.
The Journal of Allergy and Clinical Immunology
|
February 1, 2017
Ruxolitinib reverses dysregulated T helper cell responses and controls autoimmunity caused by a novel signal transducer and activator of transcription 1 (STAT1) gain-of-function mutation
Katja G Weinacht, Louis-Marie Charbonnier, Fayhan Alroqi, et al.
Frontiers in Pediatrics
|
August 17, 2019
Novel Heterozygous Mutation in <i>NFKB2</i> Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome
Alejandra Aird, Macarena Lagos, Alexander Vargas-Hernández, et al.
The Journal of Allergy and Clinical Immunology
|
March 28, 2016
A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism
Petra Netter, Sanny K Chan, Pinaki P Banerjee, et al.
The Journal of Allergy and Clinical Immunology
|
January 14, 2018
Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatment
Raquel Ruiz-García, Alexander Vargas-Hernández, Ivan K Chinn, et al.
Science (New York, N.Y.)
|
October 7, 2021
Conformer-specific photochemistry imaged in real space and time
E G Champenois, D M Sanchez, J Yang, et al.
The Journal of Allergy and Clinical Immunology
|
February 6, 2025
Clinical, immunologic, and genetic characteristics of 148 patients with natural killer cell deficiency
Manar Abdalgani, Evelyn R Hernandez, Luis A Pedroza, et al.
Page
of 34