The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Link
http://link.springer.com/content/pdf/10.1007/s10875-014-0029-0.pdf
Reference46 articles.
1. Kuehn BM. After 50 years, newborn screening continues to yield public health gains. JAMA. 2013;309:1215–7.
2. Borte S, von Döbeln U, Fasth A, et al. Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR. Blood. 2012;119:2552–5.
3. Borte S, Wang N, Óskarsdóttir S, von Döbeln U, Hammarström L. Newborn screening for primary immunodeficiencies: beyond SCID and XLA. Ann N Y Acad Sci. 2011;1246:118–30.
4. Brown L, Xu-Bayford J, Allwood Z, et al. Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening. Blood. 2011;117:3243–6.
5. Puck JM. Neonatal screening for severe combined immunodeficiency. Curr Opin Pediatr. 2011;23:667–73.
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