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Results: 1-12 |
Results: 12
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency
Authors: Notorangelo, LD Mella, P Jones, A Baisle, GD Savoldi, G Cranston, T Vihinen, M Schumacher, RF
Citation: Ld. Notorangelo et al., Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency, HUM MUTAT, 18(4), 2001, pp. 255-263
Neuroblastoma with symptomatic spinal cord compression at diagnosis: Treatment and results with 76 cases
Authors: De Bernardi, B Pianca, C Pistamiglio, P Veneselli, E Viscardi, E Pession, A Alvisi, P Carli, M Donfrancesco, A Casale, F Giuliano, MG di Montezemolo, LC Di Cataldo, A Lo Curto, M Bagnulo, S Schumacher, RF Tamburini, A Garaventa, A Clemente, L Bruzzi, P
Citation: B. De Bernardi et al., Neuroblastoma with symptomatic spinal cord compression at diagnosis: Treatment and results with 76 cases, J CL ONCOL, 19(1), 2001, pp. 183-190
Community and nosocomially acquired respiratory syncytial virus infection in a German paediatric hospital from 1988 to 1999
Authors: Berner, R Schwoerer, F Schumacher, RF Meder, M Forster, J
Citation: R. Berner et al., Community and nosocomially acquired respiratory syncytial virus infection in a German paediatric hospital from 1988 to 1999, EUR J PED, 160(9), 2001, pp. 541-547
Molecular modeling of the Jak3 kinase domains and structural basis for severe combined immunodeficiency
Authors: Vihinen, M Villa, A Mella, P Schumacher, RF Savoldi, G O'Shea, JJ Candotti, F Notarangelo, LD
Citation: M. Vihinen et al., Molecular modeling of the Jak3 kinase domains and structural basis for severe combined immunodeficiency, CLIN IMMUNO, 96(2), 2000, pp. 108-118
Complete genomic organization of the human JAK3 gene and mutation analysisin severe combined immunodeficiency by single-strand conformation polymorphism
Authors: Schumacher, RF Mella, P Badolato, R Fiorini, M Savoldi, G Giliani, S Villa, A Candotti, F Tampalini, A O'Shea, JJ Notarangelo, LD
Citation: Rf. Schumacher et al., Complete genomic organization of the human JAK3 gene and mutation analysisin severe combined immunodeficiency by single-strand conformation polymorphism, HUM GENET, 106(1), 2000, pp. 73-79
Combined immunodeficiencies due to defects in signal transduction: Defectsof the gamma(c)-JAK3 signaling pathway as a model
Authors: Notarangelo, LD Giliani, S Mella, P Schumacher, RF Mazza, C Savoldi, G Rodriguez-Perez, C Badolato, R Mazzolari, E Porta, F Candotti, F Ugazio, AG
Citation: Ld. Notarangelo et al., Combined immunodeficiencies due to defects in signal transduction: Defectsof the gamma(c)-JAK3 signaling pathway as a model, IMMUNOBIOL, 202(2), 2000, pp. 106-119
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
Authors: Notarangelo, LD Giliani, S Mazza, C Mella, P Savoldi, G Rodriguez-Perez, C Mazzolari, E Fiorini, M Duse, M Plebani, A Ugazio, AG Vihinen, M Candotti, F Schumacher, RF
Citation: Ld. Notarangelo et al., Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model, IMMUNOL REV, 178, 2000, pp. 39-48
Analysis of cytomegalovirus gene expression by transfection
Authors: Colberg-Poley, AM Soltero, VE Schumacher, RF
Citation: Am. Colberg-poley et al., Analysis of cytomegalovirus gene expression by transfection, METH MOL M, 33, 2000, pp. 67-77
Occurrence and impact of community-acquired and nosocomial rotavirus infections - a hospital-based study over 10 y
Authors: Berner, R Schumacher, RF Hameister, S Forster, J
Citation: R. Berner et al., Occurrence and impact of community-acquired and nosocomial rotavirus infections - a hospital-based study over 10 y, ACT PAEDIAT, 88, 1999, pp. 48-52
The CNS symptoms of Rotavirus infections under the age of two
Authors: Schumacher, RF Forster, J
Citation: Rf. Schumacher et J. Forster, The CNS symptoms of Rotavirus infections under the age of two, KLIN PADIAT, 211(2), 1999, pp. 61-64
Prenatal diagnosis of JAK3 deficient SCID
Authors: Schumacher, RF Mella, P Lalatta, F Fiorini, M Giliani, S Villa, A Candotti, F Notarangelo, LD
Citation: Rf. Schumacher et al., Prenatal diagnosis of JAK3 deficient SCID, PRENAT DIAG, 19(7), 1999, pp. 653-656
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis
Authors: Giliani, S Fiorini, J Mella, P Candotti, F Schumacher, RF Wengler, GS Lalatta, F Fasth, A Badolato, R Ugazio, AG Albertini, A Notarangelo, LD
Citation: S. Giliani et al., Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis, PRENAT DIAG, 19(1), 1999, pp. 36-40
Risultati: 1-12 |