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European Journal of Immunology|February 5, 1999
CD40 ligand expression deficiency in a female carrier of the X-linked hyper-IgM syndrome as a result of X chromosome lyonizationG de Saint Basile, M D Tabone, A Durandy, et al.
Archives Francaises De Pediatrie|March 1, 1982
[Immunologic study of familial lymphohistiocytosis. Eight new case reports (author's transl)]D Devictor, A Fischer, S Mamas, et al.
The Journal of Clinical Investigation|October 1, 1996
A human non-XLA immunodeficiency disease characterized by blockage of B cell development at an early proB cell stageE Meffre, F LeDeist, G de Saint-Basile, et al.
Journal of Neuroimmunology|November 13, 2009
An atypical case of X-linked lymphoproliferative disease revealed as a late cerebral lymphomaB Hervier, S Latour, D Loussouarn, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Gene therapy for hereditary immunodeficiencies]A Fischer, G de Saint-Basile, J P Disanto, et al.
European Journal of Immunology|October 1, 1988
Heterogeneity in the molecular defect leading to the leukocyte adhesion deficiencyM T Dimanche-Boitrel, A Guyot, G De Saint-Basile, et al.
European Journal of Immunology|December 1, 1994
The murine interleukin-2 receptor gamma chain gene: organization, chromosomal localization and expression in the adult thymusJ P DiSanto, S Certain, A Wilson, et al.
Bone Marrow Transplantation|July 5, 2002
Successful treatment of Griscelli syndrome with unrelated donor allogeneic hematopoietic stem cell transplantationM Aricò, M Zecca, N Santoro, et al.
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