Publicaciones en colaboración con investigadores/as de Hospital Universitario 12 de Octubre (31)

2003

  1. Mutations of CD40 ligand in two patients with hyper-IgM syndrome

    Immunobiology, Vol. 207, Núm. 4, pp. 285-294

2001

  1. A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency

    Clinical and Diagnostic Laboratory Immunology, Vol. 8, Núm. 1, pp. 133-137

  2. Novel mutations and defective protein kinase C activation of T-lymphocytes in ataxia telangiectasia

    Clinical and Experimental Immunology, Vol. 123, Núm. 3, pp. 472-480

  3. Role of Nijmegen breakage syndrome protein in specific T-lymphocyte activation pathways

    Clinical and Diagnostic Laboratory Immunology, Vol. 8, Núm. 4, pp. 757-761

2000

  1. 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, Vol. 99, Núm. 3, pp. 440-450

1999

  1. Higher incidence of autoantibodies in X-linked chronic granulomatous disease carriers: Random X-chromosome inactivation may be related to autoimmunity

    Autoimmunity, Vol. 31, Núm. 4, pp. 261-264

1998

  1. Immunodeficiency associated with anorexia nervosa is secondary and improves after refeeding

    Immunology, Vol. 94, Núm. 4, pp. 543-551

1997

  1. Cell surface phenotype and ultramicroscopic analysis of purified human enterocytes: A possible antigen-presenting cell in the intestine

    Tissue Antigens, Vol. 50, Núm. 6, pp. 586-592

  2. Retinol (vitamin A) is a cofactor in CD3-induced human T-lymphocyte activation

    Immunology, Vol. 90, Núm. 3, pp. 388-396

1996

  1. DIAGNOSTICO MOLECULAR DE INMUNODEFICIENCIAS PRIMARIAS

    Inmunologia, Vol. 15, Núm. SUPPL. 1, pp. 7-18

  2. Diploid expression of human leukocyte antigen class I and class II molecules on spermatozoa and their cyclic inverse correlation with inhibin concentration

    Biology of Reproduction, Vol. 55, Núm. 3, pp. 620-629

  3. Frequencies of hla-a24 and hla-dr4-dq8 are increased and that of hla-b blank is decreased in chronic toxic oil syndrome

    International Journal of Immunogenetics, Vol. 23, Núm. 3, pp. 211-219

  4. Herpes virus saimiri transformation of T cells in CD3γ immunodeficiency: Phenotypic and functional characterization

    Journal of Immunological Methods, Vol. 198, Núm. 2, pp. 177-186

1994

  1. Peripheral blood reduction of memory (CD29+, CD45RO+, and "Bright" CD2+ and LFA-1+) T lymphocytes in Papillon-Lefèvre syndrome

    Human Immunology, Vol. 41, Núm. 3, pp. 185-192

  2. Primary T lymphocyte immunodeficiency associated with a selective impairment of CD2, CD3, CD43 (but not CD28)-mediated signal transduction

    Clinical and Experimental Immunology, Vol. 97, Núm. 3, pp. 386-391

1993

  1. A study of DR2-LUM haplotype generation and the DRB6*0202 linkage to DRB1*1601

    Immunogenetics, Vol. 38, Núm. 6, pp. 460-461

  2. Differential contribution of C4 and HLA-DQ genes to systemic lupus erythematosus susceptibility

    Human Genetics, Vol. 91, Núm. 6, pp. 579-584

  3. Three new HLA-G alleles and their linkage disequilibria with HLA-A

    Immunogenetics, Vol. 38, Núm. 5, pp. 323-331

1992

  1. Allelic diversity at the primate major histocompatibility complex DRB6 locus

    Immunogenetics, Vol. 36, Núm. 1, pp. 33-38

  2. Comparison between HLA-DRB and DQ DNA sequences and classic serological markers as Type 11 (insulin-dependent)diabetes mellitus predictive risk markers in the Spanish population

    Diabetologia: Clinical and Experimental Diabetes and Metabolism, Vol. 35, Núm. 5, pp. 475-481