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Immunogenetics|January 1, 1993
Familial clustering of IGHC deletions and duplications: functional and molecular analysisA Bottaro, R Gallina, A Brusco, et al.Nature|February 11, 1993
Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgMU Korthäuer, D Graf, H W Mages, et al.British Journal of Haematology|June 20, 1998
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.Haematologica|April 13, 2004
Reconstitution of T-cell compartment after in utero stem cell transplantation: analysis of T-cell repertoire and thymic outputSilvia Pirovano, Luigi Daniele Notarangelo, Fabio Malacarne, et al.Science (New York, N.Y.)|October 20, 1995
Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patientsC Bordignon, L D Notarangelo, N Nobili, et al.Bone Marrow Transplantation|May 24, 2005
Hematopoietic stem cell transplantation in Omenn syndrome: a single-center experienceE Mazzolari, D Moshous, C Forino, et al.Immunology Letters|January 1, 1996
Ontogeny of CD40L [corrected] expression by activated peripheral blood lymphocytes in humansD Brugnoni, P Airò, D Graf, et al.Immunobiology|September 19, 2000
Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, P Mella, et al.Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.Bone Marrow Transplantation|April 30, 2002
B cell function after haploidentical in utero bone marrow transplantation in a patient with severe combined immunodeficiencyJ Bartolomé, F Porta, A Lafranchi, et al.Pageof 20