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Results: 1-13 |
Results: 13
Identification of WASP mutations in 14 Spanish families with Wiskott-Aldrich syndrome
Authors: Fillat, C Espanol, T Oset, M Ferrando, M Estivill, X Volpini, V
Citation: C. Fillat et al., Identification of WASP mutations in 14 Spanish families with Wiskott-Aldrich syndrome, AM J MED G, 100(2), 2001, pp. 116-121
Familial CDS deficiency due to a mutation in the CD8 alpha gene
Authors: de la Calle-Martin, O Hernandez, M Ordi, J Casamitjana, N Arostegui, JI Caragol, I Ferrando, M Labrador, M Rodriguez-Sanchez, JL Espanol, T
Citation: O. De La Calle-martin et al., Familial CDS deficiency due to a mutation in the CD8 alpha gene, J CLIN INV, 108(1), 2001, pp. 117-123
Rapid protein-based assays for the diagnosis of T-B+ severe combined immunodeficiency
Authors: Gilmour, KC Cranston, T Loughlin, S Gwyther, J Lester, T Espanol, T Hernandez, M Savoldi, G Davies, EG Abinun, M Kinnon, C Jones, A Gaspar, HB
Citation: Kc. Gilmour et al., Rapid protein-based assays for the diagnosis of T-B+ severe combined immunodeficiency, BR J HAEM, 112(3), 2001, pp. 671-676
Prognostic value of a CCR5 defective allele in pediatric HIV-1 infection
Authors: Romiti, ML Colognesi, C Cancrini, C Mas, A Berrino, M Salvatori, F Orlandi, P Jansson, M Palomba, E Plebani, A Bertran, JM Hernandez, M de Martino, M Amoroso, A Tovo, PA Rossi, P Espanol, T Scarlatti, G
Citation: Ml. Romiti et al., Prognostic value of a CCR5 defective allele in pediatric HIV-1 infection, MOL MED, 6(1), 2000, pp. 28-36
Evaluation of the putative role of C-C chemokines as protective factors ofHIV-1 infection in seronegative hemophiliacs exposed to contaminated hemoderivatives
Authors: Barretina, J Blanco, J Gutierrez, A Puig, L Altisent, C Espanol, T Caragol, I Clotet, B Este, JA
Citation: J. Barretina et al., Evaluation of the putative role of C-C chemokines as protective factors ofHIV-1 infection in seronegative hemophiliacs exposed to contaminated hemoderivatives, TRANSFUSION, 40(4), 2000, pp. 461-467
A novel CD18 genomic deletion in a patient with severe leucocyte adhesion deficiency: a possible CD2/lymphocyte function-associated antigen-1 functional association in humans
Authors: Allende, LM Hernandez, M Corell, A Garcia-perez, MA Varela, P Moreno, A Caragol, I Garcia-Martin, F Guillen-Perales, J Olive, T Espanol, T Arnaiz-Villena, A
Citation: Lm. Allende et al., A novel CD18 genomic deletion in a patient with severe leucocyte adhesion deficiency: a possible CD2/lymphocyte function-associated antigen-1 functional association in humans, IMMUNOLOGY, 99(3), 2000, pp. 440-450
Kinase mutant Btk results in atypical X-linked agammaglobulinaemia phenotype
Authors: Gaspar, HB Ferrando, M Caragol, I Hernandez, M Bertran, JM De gracia, X Lester, T Kinnon, C Ashton, E Espanol, T
Citation: Hb. Gaspar et al., Kinase mutant Btk results in atypical X-linked agammaglobulinaemia phenotype, CLIN EXP IM, 120(2), 2000, pp. 346-350
Langerhans cell deficiency in reticular dysgenesis
Authors: Emile, JF Geissmann, F Martin, OD Radford-Weiss, I Lepelletier, Y Heymer, B Espanol, T de Santes, KB Bertrand, Y Brousse, N Casanova, JL Fischer, A
Citation: Jf. Emile et al., Langerhans cell deficiency in reticular dysgenesis, BLOOD, 96(1), 2000, pp. 58-62
CCR5 genotype and human immunodeficiency virus type 1 infection in perinatally exposed infants
Authors: Villalba, N Perez-Olmeda, M de Jose, M Hernandez, M Sirera, R Espanol, T Gonzalez-Molina, A Soriano, V
Citation: N. Villalba et al., CCR5 genotype and human immunodeficiency virus type 1 infection in perinatally exposed infants, EUR J CL M, 18(5), 1999, pp. 389-391
CCR5 genotype and HIV-1 infection in perinatally-exposed infants
Authors: Mas, A Espanol, T Heredia, A Pedraza, MA Hernandez, M Caragol, I Fernando, M Bertran, JM Alcami, J Soriano, V
Citation: A. Mas et al., CCR5 genotype and HIV-1 infection in perinatally-exposed infants, J INFECTION, 38(1), 1999, pp. 9-11
Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell-depleted bone marrow transplantation - A retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society for Immunodeficiency
Authors: Bertrand, Y Landais, P Friedrich, W Gerritsen, B Morgan, G Fasth, A Cavazzana-Calvo, M Porta, F Cant, A Espanol, T Muller, S Veys, P Vossen, J Haddad, E Fischer, A
Citation: Y. Bertrand et al., Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell-depleted bone marrow transplantation - A retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society for Immunodeficiency, J PEDIAT, 134(6), 1999, pp. 740-748
Defective self-reactive antibody repertoire of serum IgM in patients with hyper-IgM syndrome
Authors: Lacroix-Desmazes, S Resnick, I Stahl, D Mouthon, L Espanol, T Levy, J Kaveri, SV Notarangelo, L Eibl, M Fischer, A Ochs, H Kazatchkine, MD
Citation: S. Lacroix-desmazes et al., Defective self-reactive antibody repertoire of serum IgM in patients with hyper-IgM syndrome, J IMMUNOL, 162(9), 1999, pp. 5601-5608
Genetic linkage of hyper-IgE syndrome to chromosome 4
Authors: Grimbacher, B Schaffer, AA Holland, SM Davis, J Gallin, JI Malech, HL Atkinson, TP Belohradsky, BH Buckley, RH Cossu, F Espanol, T Garty, BZ Matamoros, N Myers, LA Nelson, RP Ochs, HD Renner, ED Wellinghausen, N Puck, JM
Citation: B. Grimbacher et al., Genetic linkage of hyper-IgE syndrome to chromosome 4, AM J HU GEN, 65(3), 1999, pp. 735-744
Risultati: 1-13 |