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The Journal of Allergy and Clinical Immunology|July 2, 2013
Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 yearsAntonia Kwan, Joseph A Church, Morton J Cowan, et al.
The Journal of Allergy and Clinical Immunology|April 30, 2013
Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicismAmy P Hsu, Kathryn J Sowerwine, Monica G Lawrence, et al.
Immunity|August 1, 2025
Innate-like memory T cells rapidly emerge in humans after gene therapy for SCID-X1Anoop Babu Vasandan, Hossam A Abdelsamed, Shannon K Boi, et al.
The Journal of Allergy and Clinical Immunology|December 3, 2013
Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experienceWilliam T Shearer, Elizabeth Dunn, Luigi D Notarangelo, et al.
Human Gene Therapy|September 10, 2016
Lentivirus Mediated Correction of Artemis-Deficient Severe Combined ImmunodeficiencyDivya Punwani, Misako Kawahara, Jason Yu, et al.
The Journal of Allergy and Clinical Immunology|November 20, 2012
Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantationKarin R Engelhardt, Neil Shah, Intan Faizura-Yeop, et al.
Frontiers in Immunology|August 15, 2022
Investigation of the causal etiology in a patient with T-B+NK+ immunodeficiencyRobert Sertori, Jian-Xin Lin, Esteban Martinez, et al.
The Journal of Allergy and Clinical Immunology. in Practice|September 24, 2017
Autosomal Dominant Hyper-IgE Syndrome in the USIDNET RegistryYael Gernez, Alexandra F Freeman, Steven M Holland, et al.
Genome Research|March 3, 2004
Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide arrayHajime Matsuzaki, Halina Loi, Shoulian Dong, et al.
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