Cutaneous manifestations of maternal engraftment in patients with severe combined immunodeficiency: a clinicopathologic study

Author:

Denianke KS,Frieden IJ,Cowan MJ,Williams ML,McCalmont TH

Publisher

Springer Science and Business Media LLC

Subject

Transplantation,Hematology

Reference17 articles.

1. Buckley R, Schiff R, Schiff S et al. Human severe combined immunodeficiency: genetic, phenotypic and functional diversity in one hundred eight infants J Pediatr 1997 130: 378–387

2. Dror Y, Gallagher R, Wara DW et al. Immune reconstitution in severe combined immunodeficiency disease after lectin-treated, T-cell depleted haplocompatible bone marrow transplantation Blood 1993 8: 2021–2030

3. Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G et al. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease Science 2000 288: 669–671

4. Geha R, Reinherz E . Identification of circulating maternal T and B lymphocytes in uncomplicated severe combined immunodeficiency by HLA typing of subpopulations of T cells separated by the fluorescence-activated cell sorter and of Epstein–Barr virus-derived B cell lines J Immunol 1983 130: 2493–2495

5. Knobloch C, Goldman S, Friedrich W . Limited T cell receptor diversity of transplacentally acquired maternal T cells in severe combined immunodeficiency J Immunol 1991 146: 4157–4164

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