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Familial CD8 deficiency due to a mutation in the CD8 alpha gene

The Journal of clinical investigation, 2001-07, Vol.108 (1), p.117-123

2001

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Mutations in the Fas gene found in Spanish ALPS (autoimmune lymphoproliferative syndrome) patients

Journal of translational medicine, 2010-11, Vol.8 (S1), p.P20-P20, Article P20

2010

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Severe and recurrent episodes of bronchiolitis obliterans organising pneumonia associated with indolent CD4+ CD8+ T-cell leukaemia

The European respiratory journal, 2008-06, Vol.31 (6), p.1368-1372

2008

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A novel HLA-B35 variant, HLA-B35:02:03, identified by sequence-based typing in a bone marrow donor

Tissue antigens, 2010-08, Vol.76 (2), p.152-153

2010

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A novel HLA-Cw07 variant, HLA-Cw0760, identified by sequence-based typing in a bone marrow donor

Tissue antigens, 2009-08, Vol.74 (2), p.172-173

2009

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B cells and monocytes are not developmentally affected in a case of reticular dysgenesis

Clinical and experimental immunology, 1997-12, Vol.110 (3), p.392-396

1997

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Identification of a novel HLA-DRB1 allele, DRB10108, by sequence-based DRB typing in two siblings

Tissue antigens, 2002-04, Vol.59 (4), p.350-351

2002

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Impaired post‐transcriptional expression of interleukin‐2 receptor in pokeweed mitogen‐activated T cells

European journal of immunology, 1992-04, Vol.22 (4), p.897-902

1992

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Hacia dónde va la Sociedad Española de Inmunología?

Inmunología (1987), 2013, Vol.32 (1), p.35-39

2013

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Loss of heterozygosity of p53 gene and p53 protein expression in human colorectal carcinomas

Cancer research (Chicago, Ill.), 1991-08, Vol.51 (16), p.4436-4442

1991

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Langerhans cell deficiency in reticular dysgenesis

Blood, 2000-07, Vol.96 (1), p.58-62

2000

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Una nueva página web para todos

Inmunología (1987), 2013, Vol.32 (4), p.121-122

2013

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The Vβ complementarity determining region 1 of a major histocompatibility complex (MHC) class I-restricted T cell receptor is involved in the recognition of peptide/MHC I and superantigen/MHC II complex

The Journal of experimental medicine, 1994-04, Vol.179 (4), p.1087-1097

1994

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The polymorphonuclear neutrophil Fc gamma RIIIb deficiency is more frequent than hitherto assumed

Blood, 1995-11, Vol.86 (10), p.3999-3999

1995

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Induction of interleukin 2 (IL2) and interferon‐γ and enhancement of IL2 receptor expression by a CD26 monoclonal antibody

European journal of immunology, 1991-04, Vol.21 (4), p.1085-1088

1991

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MspI polymorphism of the human p53 gene

Nucleic acids research, 1990-08, Vol.18 (16), p.4963-4963

1990

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AccII polymorphism of the p53 gene

Nucleic acids research, 1990-08, Vol.18 (16), p.4963-4963

1990

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Induction of interleukin 2 (IL 2) and interferon-gamma and enhancement of IL 2 receptor expression by a CD26 monoclonal antibody

European journal of immunology, 1991-04, Vol.21 (4), p.1085-1088

1991

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A novel HLA-B35 variant, HLA-B 35:02:03, identified by sequence-based typing in a bone marrow donor

Tissue antigens, 2010-05, p.no-no

2010

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Prevalence of erectile dysfunction in Spanish primary care setting and its association with cardiovascular risk factors and cardiovascular diseases. SIMETAP-ED study

Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis, 2019-05, Vol.31 (3), p.101-110

2019

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LA ARITMÉTICA QUE ENCARNA EL CUERPO EN QUE NACÍ DE GUADALUPE NETTEL

Acta literaria, 2022-07, Vol.64 (64), p.59-77

2022

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Características del síndrome de lisis tumoral, en pacientes pediátricos oncológicos: Un estudio observacional de centro único

Oncología, 2023-12, Vol.33 (3), p.228-238

2023

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Mspl polymorphism of the human p53 gene

Nucleic acids research, 1990-08, Vol.18 (16), p.4963-4963, Article 4963

1990

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Gripe pandémica A/H1N1 2009 atendida en un centro de salud urbano de Madrid

Semergen, medicina de familia, 2011-11, Vol.37 (9), p.449-454

2011

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Familial CD8 deficiency due to a mutation in the CD8 alpha gene

Mutations in the Fas gene found in Spanish ALPS (autoimmune lymphoproliferative syndrome) patients

Severe and recurrent episodes of bronchiolitis obliterans organising pneumonia associated with indolent CD4+ CD8+ T-cell leukaemia

A novel HLA-B35 variant, HLA-B35:02:03, identified by sequence-based typing in a bone marrow donor

A novel HLA-Cw07 variant, HLA-Cw0760, identified by sequence-based typing in a bone marrow donor

B cells and monocytes are not developmentally affected in a case of reticular dysgenesis

Identification of a novel HLA-DRB1 allele, DRB10108, by sequence-based DRB typing in two siblings

Impaired post‐transcriptional expression of interleukin‐2 receptor in pokeweed mitogen‐activated T cells

Hacia dónde va la Sociedad Española de Inmunología?

Loss of heterozygosity of p53 gene and p53 protein expression in human colorectal carcinomas

Langerhans cell deficiency in reticular dysgenesis

Una nueva página web para todos

The Vβ complementarity determining region 1 of a major histocompatibility complex (MHC) class I-restricted T cell receptor is involved in the recognition of peptide/MHC I and superantigen/MHC II complex

The polymorphonuclear neutrophil Fc gamma RIIIb deficiency is more frequent than hitherto assumed

Induction of interleukin 2 (IL2) and interferon‐γ and enhancement of IL2 receptor expression by a CD26 monoclonal antibody

MspI polymorphism of the human p53 gene

AccII polymorphism of the p53 gene

Induction of interleukin 2 (IL 2) and interferon-gamma and enhancement of IL 2 receptor expression by a CD26 monoclonal antibody

A novel HLA-B35 variant, HLA-B 35:02:03, identified by sequence-based typing in a bone marrow donor

Prevalence of erectile dysfunction in Spanish primary care setting and its association with cardiovascular risk factors and cardiovascular diseases. SIMETAP-ED study

Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

LA ARITMÉTICA QUE ENCARNA EL CUERPO EN QUE NACÍ DE GUADALUPE NETTEL

Características del síndrome de lisis tumoral, en pacientes pediátricos oncológicos: Un estudio observacional de centro único

Mspl polymorphism of the human p53 gene

Gripe pandémica A/H1N1 2009 atendida en un centro de salud urbano de Madrid

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