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L D Notarangelo

Showing results (151-160 of 165) with videos related to

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Journal of Medical Genetics|July 11, 2006
Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosisA Santoro, S Cannella, G Bossi, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 25, 2001
Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgMS Ferrari, S Giliani, A Insalaco, et al.
Molecular and Cellular Biology|June 8, 2001
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein familyB W Richter, S S Mir, L J Eiben, et al.
Blood Cancer Journal|September 15, 2021
Production and persistence of specific antibodies in COVID-19 patients with hematologic malignancies: role of rituximabC Cattaneo, V Cancelli, L Imberti, et al.
Blood|November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiencyF Candotti, S A Oakes, J A Johnston, et al.
British Journal of Haematology|September 6, 2023
Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke systemV Munaretto, P Corti, E Bertoni, et al.
Cell|September 28, 2000
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)P Revy, T Muto, Y Levy, et al.
Genes and Immunity|January 10, 2002
Unexpected and variable phenotypes in a family with JAK3 deficiencyD M Frucht, M Gadina, G J Jagadeesh, et al.
Advances in Genetics|October 19, 2000
Primary immunodeficiency mutation databasesM Vihinen, F X Arredondo-Vega, J L Casanova, et al.
The Journal of Pediatrics|July 1, 1997
Clinical spectrum of X-linked hyper-IgM syndromeJ Levy, T Espanol-Boren, C Thomas, et al.
Pageof 17

Showing results (151-160 of 165) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|July 11, 2006
Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosisA Santoro, S Cannella, G Bossi, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 25, 2001
Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgMS Ferrari, S Giliani, A Insalaco, et al.
Molecular and Cellular Biology|June 8, 2001
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein familyB W Richter, S S Mir, L J Eiben, et al.
Blood Cancer Journal|September 15, 2021
Production and persistence of specific antibodies in COVID-19 patients with hematologic malignancies: role of rituximabC Cattaneo, V Cancelli, L Imberti, et al.
Blood|November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiencyF Candotti, S A Oakes, J A Johnston, et al.
British Journal of Haematology|September 6, 2023
Acute chest syndrome in children with sickle cell disease: Data from a national AIEOP cohort identify priority areas of intervention in a hub-and-spoke systemV Munaretto, P Corti, E Bertoni, et al.
Cell|September 28, 2000
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)P Revy, T Muto, Y Levy, et al.
Genes and Immunity|January 10, 2002
Unexpected and variable phenotypes in a family with JAK3 deficiencyD M Frucht, M Gadina, G J Jagadeesh, et al.
Advances in Genetics|October 19, 2000
Primary immunodeficiency mutation databasesM Vihinen, F X Arredondo-Vega, J L Casanova, et al.
The Journal of Pediatrics|July 1, 1997
Clinical spectrum of X-linked hyper-IgM syndromeJ Levy, T Espanol-Boren, C Thomas, et al.
Pageof 17