#Severe combined immunodeficiency scid update

Updated April 5, 2007.īertrand Y, Landais P, Friedrich W, et al. Chest Radiographs for Distinguishing ADA-SCID from Other Forms of SCID. Verhagen MV, Trevisan V, Adu J, Owens CM, Booth C, Calder A. TREC Based Newborn Screening for Severe Combined Immunodeficiency Disease: A Systematic Review. Van der Spek J, Groenwold RH, van der Burg M, van Montfrans JM. Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia. Ridanpaa M, van Eenennaam H, Pelin K, et al. Clinical spectrum of X-linked hyper-IgM syndrome. Levy J, Espanol-Boren T, Thomas C, et al. Clinical characteristics and mutation analysis of X-linked severe combined immunodeficiency in China. Zhang C, Zhang ZY, Wu JF, Tang XM, Yang XQ, Jiang LP, et al. Severe Combined Immunodeficiency (SCID) in Canadian Children: A National Surveillance Study. Rozmus J, Junker A, Thibodeau ML, Grenier D, Turvey SE, Yacoub W, et al. Screening for severe combined immunodeficiency in neonates. Newborn screening for severe T and B cell immunodeficiency in Israel: a pilot study. Somech R, Lev A, Simon AJ, Korn D, Garty BZ, Amariglio N, et al. Newborn Screening for Severe Combined Immunodeficiency The Wisconsin Experience (2008-2011). Verbsky JW, Baker MW, Grossman WJ, Hintermeyer M, Dasu T, Bonacci B, et al. Successful Handling of Disseminated BCG Disease in a Child with Severe Combined Immunodeficiency. 39 (3):194-205.īacalhau S, Freitas C, Valente R, Barata D, Neves C, Schäfer K, et al. History and current status of newborn screening for severe combined immunodeficiency. Chronic cutaneous cytomegalovirus infection in a patient with severe combined immunodeficiency syndrome. 117(2 suppl mini-primer):S435-41.Ĭachafeiro T, Escobar G, Bakos L, Bakos R.

#Severe combined immunodeficiency scid update

Update on primary immunodeficiency diseases. Updated August 21, 2006.īonilla FA, Geha RS. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.

Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. 117(5):1270-81.Ĭavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, et al. Homeostatically proliferating CD4 T cells are involved in the pathogenesis of an Omenn syndrome murine model. Khiong K, Murakami M, Kitabayashi C, et al. Gene therapy for severe combined immunodeficiency: are we there yet?. Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders. Stray-Pedersen A, Sorte HS, Samarakoon P, Gambin T, Chinn IK, et.