Showing results (11-20 of 22) with videos related to
Sort By:
Pageof 3
The Journal of Allergy and Clinical Immunology|May 7, 2014
Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotypeHuie Jing, Qian Zhang, Yu Zhang, et al.Frontiers in Immunology|August 8, 2014
Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndromeAmy E O'Connell, Stefano Volpi, Kerry Dobbs, et al.The Journal of Clinical Investigation|June 3, 2020
Disease-associated CTNNBL1 mutation impairs somatic hypermutation by decreasing nuclear AIDMarcel Kuhny, Lisa R Forbes, Elif Çakan, et al.Frontiers in Immunology|December 28, 2020
Case Report: Secondary Hemophagocytic Lymphohistiocytosis With Disseminated Infection in Chronic Granulomatous Disease-A Serious Cause of MortalityJacqueline D Squire, Stephanie N Vazquez, Angela Chan, et al.Journal of Clinical Immunology|July 3, 2013
The natural history of children with severe combined immunodeficiency: baseline features of the first fifty patients of the primary immune deficiency treatment consortium prospective study 6901Christopher C Dvorak, Morton J Cowan, Brent R Logan, et al.The Journal of Allergy and Clinical Immunology|February 28, 2016
Adoptive immunotherapy for primary immunodeficiency disorders with virus-specific T lymphocytesSwati Naik, Sarah K Nicholas, Caridad A Martinez, et al.Science Translational Medicine|April 22, 2016
Lentiviral hematopoietic stem cell gene therapy for X-linked severe combined immunodeficiencySuk See De Ravin, Xiaolin Wu, Susan Moir, et al.Blood Advances|December 1, 2022
Cord blood transplantation for nonmalignant disorders: early functional immunity and high survivalCaridad Martinez, Paibel Aguayo-Hiraldo, Natalia Chaimowitz, et al.American Journal of Human Genetics|June 17, 2014
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasiaAsbjørg Stray-Pedersen, Paul H Backe, Hanne S Sorte, et al.Blood|October 8, 2010
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the diseaseClaire Booth, Kimberly C Gilmour, Paul Veys, et al.Pageof 3