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L D Notarangelo

Showing results (51-60 of 165) with videos related to

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Human Mutation|October 23, 2001
Eleven novel JAK3 mutations in patients with severe combined immunodeficiency-including the first patients with mutations in the kinase domainP Mella, R F Schumacher, T Cranston, et al.
Clinical and Experimental Immunology|September 1, 1983
IgM and IgD concentrations in the serum and secretions of children with selective IgA deficiencyA Plebani, E Mira, E Mevio, et al.
Biochemical and Biophysical Research Communications|March 1, 2000
Structural basis for SH2D1A mutations in X-linked lymphoproliferative diseaseI Lappalainen, S Giliani, R Franceschini, et al.
Lancet (London, England)|September 2, 1995
Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNAG S Wengler, L D Notarangelo, S Giliani, et al.
European Journal of Pediatrics|April 1, 1994
Naive and memory T-cells in HIV-infected childrenM Duse, P Airò, E Prati, et al.
European Journal of Pediatrics|April 1, 1993
Intravenous immunoglobulin in two children with Guillain-Barré syndromeL D Notarangelo, M Duse, S Tiberti, et al.
European Journal of Immunology|December 12, 1997
In vitro cell death of activated lymphocytes in Omenn's syndromeD Brugnoni, P Airò, F Facchetti, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1994
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and pubertyF Buzi, L D Notarangelo, A Plebani, et al.
Progress in Clinical and Biological Research|January 1, 1982
Metaphyseal dysplasia, type SchmidG Beluffi, P Fiori, A Schifino, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of RAG-deficient Omenn syndromeA Villa, F Bozzi, C Sobacchi, et al.
Pageof 17

Showing results (51-60 of 165) with videos related to

Sort By:
Pageof 17
Human Mutation|October 23, 2001
Eleven novel JAK3 mutations in patients with severe combined immunodeficiency-including the first patients with mutations in the kinase domainP Mella, R F Schumacher, T Cranston, et al.
Clinical and Experimental Immunology|September 1, 1983
IgM and IgD concentrations in the serum and secretions of children with selective IgA deficiencyA Plebani, E Mira, E Mevio, et al.
Biochemical and Biophysical Research Communications|March 1, 2000
Structural basis for SH2D1A mutations in X-linked lymphoproliferative diseaseI Lappalainen, S Giliani, R Franceschini, et al.
Lancet (London, England)|September 2, 1995
Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNAG S Wengler, L D Notarangelo, S Giliani, et al.
European Journal of Pediatrics|April 1, 1994
Naive and memory T-cells in HIV-infected childrenM Duse, P Airò, E Prati, et al.
European Journal of Pediatrics|April 1, 1993
Intravenous immunoglobulin in two children with Guillain-Barré syndromeL D Notarangelo, M Duse, S Tiberti, et al.
European Journal of Immunology|December 12, 1997
In vitro cell death of activated lymphocytes in Omenn's syndromeD Brugnoni, P Airò, F Facchetti, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1994
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and pubertyF Buzi, L D Notarangelo, A Plebani, et al.
Progress in Clinical and Biological Research|January 1, 1982
Metaphyseal dysplasia, type SchmidG Beluffi, P Fiori, A Schifino, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of RAG-deficient Omenn syndromeA Villa, F Bozzi, C Sobacchi, et al.
Pageof 17