Publicaciones en las que colabora con Alfredo Corell Almuzara (53)

2018

  1. Inmunogenética

    Síntesis

2014

  1. Una mirada hacia la excelencia docente desde las TICs

    La innovación educativa para transformar la sociedad multicultural: el papel de las universidades (Foro Internacional de Innovación Universitaria), pp. 95-105

2013

  1. A new webpage for everyone

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

2010

  1. Inmunología: biología y patología del sistema inmunitario

    Editorial Médica Panamericana

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. 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