Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell–depleted bone marrow transplantationA retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society for Immunodeficiency-Reference-Cited by-同舟云学术

Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell–depleted bone marrow transplantationA retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society for Immunodeficiency

Published:1999-06 Issue:6 Volume:134 Page:740-748
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Bertrand Yves,Landais Paul,Friedrich Wilhelm,Gerritsen Bert,Morgan Gareth,Fasth Anders,Cavazzana-Calvo Marina,Porta Fulvio,Cant Andrew,Espanol Theresa,Müller Susannah,Veys Paul,Vossen Jack,Haddad Elie,Fischer Alain

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference27 articles.

1. Primary immunodeficiency diseases;WHO;Clin Exp Immunol,1997

2. Selective defect of precursor T cells associated with apparently normal B lymphocytes in SCID;Griscelli;J Pediatr,1978

3. Immunological reconstitution of sex-linked lymphopenic immunological deficiency;Gatti;Lancet,1968

4. Transplantation for severe combined immunodeficiency with HLA-A, B, D and DR incompatible parental marrow cells fractionated by soybean agglutinin and sheep red blood cells;Reisner;Blood,1983

5. Analysis of 462 transplantations from unrelated donors facilitated by the National Marrow Donor Program;Kernan;N Engl J Med,1993

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