Severe combined immunodeficiencies and related disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://www.nature.com/articles/nrdp201561.pdf
Reference162 articles.
1. Buckley, R. H. Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution. Annu. Rev. Immunol. 22, 625–655 (2004).
2. Fischer, A. et al. Severe combined immunodeficiency. A model disease for molecular immunology and therapy. Immunol. Rev. 203, 98–109 (2005). Thorough descriptions of SCID conditions.
3. Conley, M. E., Beckwith, J. B., Mancer, J. F. & Tenckhoff, L. The spectrum of the DiGeorge syndrome. J. Pediatr. 94, 883–890 (1979).
4. Glanzmann, E. & Riniker, P. [Essential lymphocytophthisis; new clinical aspect of infant pathology]. Ann. Paediatr. 175, 1–32 (1950).
5. Kwan, A. et al. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States. JAMA 312, 729–738 (2014). A description of the effectiveness of newborn screening for SCID.
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