Publicaciones en las que colabora con Alfredo Corell Almuzara (48)

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. 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

  6. 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

  7. 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

  8. 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

  2. Mesa redonda. Inmunología para pediatras: inmunodeficiencias primarias. Técnicas diagnósticas

    XX Congreso Español Extraordinario de Pediatría: 10-13 de junio de 1998, Palacio de Congresos de Torremolinos (Málaga)

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

  5. 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