Publicaciones en colaboración con investigadores/as de Universidad Complutense de Madrid (20)

2019

  1. Component-resolved diagnosis in allergic disease: Utility and limitations

    Clinica Chimica Acta, Vol. 489, pp. 219-224

2013

  1. A new webpage for everyone

    Inmunologia, Vol. 32, Núm. 4, pp. 121-122

2001

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

    European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 201

  2. Cathepsin C gene: First compound heterozygous patient with Papillon-Lefèvre syndrome and a novel symptomless mutation

    Human mutation, Vol. 17, Núm. 2, pp. 152-153

  3. Cathepsin C gene: First compound heterozygous patient with papillon-lefevre syndrome, a new symptomless mutation and its possible regulation by retinoids

    European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 330

  4. Cell surface phenotype and cytokine secretion in Caco-2 cell cultures: Lack of HLA class II molecules and increased RANTES production and IL-2 transcription upon stimulation with IL-1β

    European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 332

  5. New mutations and defective phorbol myristate acetate activation of T-lvmphocytes in ataxia telangiectasia patients

    European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 330

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

1998

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

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

1997

  1. Lupus like lesions in a patient with x-linked chronic granulomatous disease and recombinant x chromosome

    Dermatology, Vol. 195, Núm. 3, pp. 280-283

1996

  1. 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

  2. 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

  3. Primate DRB6 gene expression and evolution: A study in Macaca mulatta and Cercopithecus aethiops

    Tissue Antigens, Vol. 47, Núm. 3, pp. 222-227

1995

  1. Diseases involving the T-cell receptor/CD3 complex

    Critical Reviews in Oncology and Hematology, Vol. 19, Núm. 2, pp. 131-147

  2. Immunosuppression induced by hepatitis C virus infection reduces acute renal-transplant rejection

    The Lancet

1994

  1. C4 gene polymorphism in primates: evolution, generation, and Chido and Rodgers antigenicity

    Immunogenetics, Vol. 40, Núm. 6, pp. 381-396

1993

  1. New DNA sequences for the human complement gene C4

    Molecular Immunology, Vol. 30, Núm. 6, pp. 515-516

1992

  1. Human T-cell activation deficiencies

    Immunology Today, Vol. 13, Núm. 7, pp. 259-265

  2. Lymphomatoid papulosis: a study of 18 cases

    Journal of the European Academy of Dermatology and Venereology, Vol. 1, Núm. 3, pp. 205-216

  3. Primary Immunodeficiency Caused by Mutations in the Gene Encoding the CD3-γ Subunit of the T-Lymphocyte Receptor

    New England Journal of Medicine, Vol. 327, Núm. 8, pp. 529-533