Publicaciones en las que colabora con Miguel Ángel García Pérez (9)

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 IFN gamma receptor 1 provokes severe immunodeficiency

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

  2. 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

  3. 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

  4. 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

  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

  6. 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

  7. 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