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Gulbu Uzel

Showing results (71-80 of 168) with videos related to

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Journal of Clinical Immunology|December 16, 2014
Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN diseaseFatima Dhalla, Sarah Murray, Ross Sadler, et al.
Frontiers in Immunology|July 30, 2019
<i>STAT1</i> Gain-of-Function Mutations Cause High Total STAT1 Levels With Normal DephosphorylationOfer Zimmerman, Peter Olbrich, Alexandra F Freeman, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|January 25, 2011
Interleukin-12 receptor β1 deficiency predisposing to disseminated CoccidioidomycosisDonald C Vinh, Brian Schwartz, Amy P Hsu, et al.
Autophagy|November 17, 2015
TOR-dependent post-transcriptional regulation of autophagyGuowu Hu, Travis McQuiston, Amélie Bernard, et al.
Journal of Clinical Immunology|October 17, 2021
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8Stuart G Tangye, Paul E Gray, Bethany A Pillay, et al.
Journal of Human Immunity|May 22, 2026
A systematic literature review of CVID reveals pervasive detrimental noninfectious manifestationsG Michelle Ducasa, Rebecca A Marsh, Ali Mojebi, et al.
Blood|March 10, 2012
Anti-CD20 (rituximab) therapy for anti-IFN-γ autoantibody-associated nontuberculous mycobacterial infectionSarah K Browne, Rifat Zaman, Elizabeth P Sampaio, et al.
Blood|February 23, 2013
Loss-of-function of the protein kinase C δ (PKCδ) causes a B-cell lymphoproliferative syndrome in humansHye Sun Kuehn, Julie E Niemela, Andreia Rangel-Santos, et al.
Frontiers in Immunology|March 21, 2019
Disseminated and Congenital Toxoplasmosis in a Mother and Child With Activated PI3-Kinase δ Syndrome Type 2 (APDS2): Case Report and a Literature Review of Toxoplasma Infections in Primary ImmunodeficienciesDjuro Karanovic, Ian C Michelow, Anthony R Hayward, et al.
The New England Journal of Medicine|December 31, 2010
Residual NADPH oxidase and survival in chronic granulomatous diseaseDouglas B Kuhns, W Gregory Alvord, Theo Heller, et al.
Pageof 17

Showing results (71-80 of 168) with videos related to

Sort By:
Pageof 17
Journal of Clinical Immunology|December 16, 2014
Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN diseaseFatima Dhalla, Sarah Murray, Ross Sadler, et al.
Frontiers in Immunology|July 30, 2019
<i>STAT1</i> Gain-of-Function Mutations Cause High Total STAT1 Levels With Normal DephosphorylationOfer Zimmerman, Peter Olbrich, Alexandra F Freeman, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|January 25, 2011
Interleukin-12 receptor β1 deficiency predisposing to disseminated CoccidioidomycosisDonald C Vinh, Brian Schwartz, Amy P Hsu, et al.
Autophagy|November 17, 2015
TOR-dependent post-transcriptional regulation of autophagyGuowu Hu, Travis McQuiston, Amélie Bernard, et al.
Journal of Clinical Immunology|October 17, 2021
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8Stuart G Tangye, Paul E Gray, Bethany A Pillay, et al.
Journal of Human Immunity|May 22, 2026
A systematic literature review of CVID reveals pervasive detrimental noninfectious manifestationsG Michelle Ducasa, Rebecca A Marsh, Ali Mojebi, et al.
Blood|March 10, 2012
Anti-CD20 (rituximab) therapy for anti-IFN-γ autoantibody-associated nontuberculous mycobacterial infectionSarah K Browne, Rifat Zaman, Elizabeth P Sampaio, et al.
Blood|February 23, 2013
Loss-of-function of the protein kinase C δ (PKCδ) causes a B-cell lymphoproliferative syndrome in humansHye Sun Kuehn, Julie E Niemela, Andreia Rangel-Santos, et al.
Frontiers in Immunology|March 21, 2019
Disseminated and Congenital Toxoplasmosis in a Mother and Child With Activated PI3-Kinase δ Syndrome Type 2 (APDS2): Case Report and a Literature Review of Toxoplasma Infections in Primary ImmunodeficienciesDjuro Karanovic, Ian C Michelow, Anthony R Hayward, et al.
The New England Journal of Medicine|December 31, 2010
Residual NADPH oxidase and survival in chronic granulomatous diseaseDouglas B Kuhns, W Gregory Alvord, Theo Heller, et al.
Pageof 17