Treatment of infants identified as having severe combined immunodeficiency by means of newborn screening
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference35 articles.
1. Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution;Buckley;Annu Rev Immunol,2004
2. Primary immunodeficiency diseases: a molecular and genetic approach,2013
3. Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience;Shearer;J Allergy Clin Immunol,2014
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1. 209 Aggressive immunosuppressive therapy is beneficial early on in reducing autoreactive T cell proliferation in Omenn syndrome/Severe combined immunodeficiency;Clinical Immunology;2024-05
2. Shorter birth length and decreased T-cell production and function predict severe infections in children with non–severe combined immunodeficiency cartilage–hair hypoplasia;Journal of Allergy and Clinical Immunology: Global;2024-02
3. Immunology of the Fetus and Newborn;Avery's Diseases of the Newborn;2024
4. Efficient screening strategies for severe combined immunodeficiencies in newborns;Expert Review of Molecular Diagnostics;2023-08-21
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