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Blood
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August 27, 2013
Innate immune control of EBV-infected B cells by invariant natural killer T cells
Brian K Chung, Kevin Tsai, Lenka L Allan, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
|
January 15, 2021
Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy
Bhavi P Modi, Kate L Del Bel, Susan Lin, et al.
HGG Advances
|
December 2, 2023
Gain-of-function MARK4 variant associates with pediatric neurodevelopmental disorder and dysmorphism
Simran Samra, Mehul Sharma, Maryam Vaseghi-Shanjani, et al.
The Journal of Experimental Medicine
|
April 27, 2021
SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
Vanessa Sancho-Shimizu, Petter Brodin, Aurélie Cobat, et al.
Scientific Reports
|
December 29, 2024
The role of C-reactive protein and ferritin in the diagnosis of HLH, adult-onset still's disease, and COVID-19 cytokine storm
Mariam Goubran, Caroline Spaner, Sophie Stukas, et al.
Lancet Regional Health. Americas
|
March 29, 2022
Reduced fixed dose tocilizumab 400 mg IV compared to weight-based dosing in critically ill patients with COVID-19: A before-after cohort study
Sophie Stukas, George Goshua, Angus Kinkade, et al.
BMC Pediatrics
|
January 21, 2021
Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report
Geraldine Blanchard-Rohner, Robert J Ragotte, Anne K Junker, et al.
The Journal of Allergy and Clinical Immunology
|
May 1, 2016
Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiency
Waleed Al-Herz, Julia I Chu, Jet van der Spek, et al.
The Journal of Experimental Medicine
|
May 20, 2025
A multimorphic variant in ThPOK causes an inborn error of immunity with T cell defects and fibrosis
Maryam Vaseghi-Shanjani, Mehul Sharma, Pariya Yousefi, et al.
Molecular Genetics and Metabolism Reports
|
June 21, 2018
<i>De novo ATP1A3</i> and compound heterozygous <i>NLRP3</i> mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome
Alcy Torres, Catherine A Brownstein, Sahil K Tembulkar, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Blood
|
August 27, 2013
Innate immune control of EBV-infected B cells by invariant natural killer T cells
Brian K Chung, Kevin Tsai, Lenka L Allan, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
|
January 15, 2021
Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy
Bhavi P Modi, Kate L Del Bel, Susan Lin, et al.
HGG Advances
|
December 2, 2023
Gain-of-function MARK4 variant associates with pediatric neurodevelopmental disorder and dysmorphism
Simran Samra, Mehul Sharma, Maryam Vaseghi-Shanjani, et al.
The Journal of Experimental Medicine
|
April 27, 2021
SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
Vanessa Sancho-Shimizu, Petter Brodin, Aurélie Cobat, et al.
Scientific Reports
|
December 29, 2024
The role of C-reactive protein and ferritin in the diagnosis of HLH, adult-onset still's disease, and COVID-19 cytokine storm
Mariam Goubran, Caroline Spaner, Sophie Stukas, et al.
Lancet Regional Health. Americas
|
March 29, 2022
Reduced fixed dose tocilizumab 400 mg IV compared to weight-based dosing in critically ill patients with COVID-19: A before-after cohort study
Sophie Stukas, George Goshua, Angus Kinkade, et al.
BMC Pediatrics
|
January 21, 2021
Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report
Geraldine Blanchard-Rohner, Robert J Ragotte, Anne K Junker, et al.
The Journal of Allergy and Clinical Immunology
|
May 1, 2016
Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiency
Waleed Al-Herz, Julia I Chu, Jet van der Spek, et al.
The Journal of Experimental Medicine
|
May 20, 2025
A multimorphic variant in ThPOK causes an inborn error of immunity with T cell defects and fibrosis
Maryam Vaseghi-Shanjani, Mehul Sharma, Pariya Yousefi, et al.
Molecular Genetics and Metabolism Reports
|
June 21, 2018
<i>De novo ATP1A3</i> and compound heterozygous <i>NLRP3</i> mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome
Alcy Torres, Catherine A Brownstein, Sahil K Tembulkar, et al.
Page
of 5