ANTONIO
ARNAIZ VILLENA
Profesor emérito
Miguel Ángel
García Pérez
Publicaciones en las que colabora con Miguel Ángel García Pérez (11)
2001
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A point mutation in a domain of IFN gamma receptor 1 provokes severe immunodeficiency
European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 201
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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
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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
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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
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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
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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
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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
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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
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Fourteen years' follow-up of an autoimmune patient lacking the CD3γ subunit of the T-lymphocyte receptor [8]
Blood
1998
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Immunodeficiency associated with anorexia nervosa is secondary and improves after refeeding
Immunology, Vol. 94, Núm. 4, pp. 543-551
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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)