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Polymorphisms of Pyrimidine Pathway Enzymes Encoding Genes and HLA-B40∶01 Carriage in Stavudine-Associated Lipodystrophy in HIV-Infected Patients

PloS one, 2013-06, Vol.8 (6), p.e67035

2013

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Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations

Journal of allergy and clinical immunology, 2018-02, Vol.141 (2), p.704-717.e5

2018

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Inherited human ezrin deficiency impairs adaptive immunity

Journal of allergy and clinical immunology, 2023-10, Vol.152 (4), p.997-1009.e11

2023

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Anti-NF155 chronic inflammatory demyelinating polyradiculoneuropathy strongly associates to HLA-DRB15

Journal of neuroinflammation, 2017-11, Vol.14 (1), p.224-224, Article 224

2017

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Non‐myeloablative hematopoietic stem cell transplantation in the treatment of severe idiopathic CD4+ lymphocytopenia

European journal of haematology, 2011-07, Vol.87 (1), p.87-91

2011

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A novel gain-of-function STAT1 mutation resulting in basal phosphorylation of STAT1 and increased distal IFN-γ-mediated responses in chronic mucocutaneous candidiasis

Molecular immunology, 2015-12, Vol.68 (2), p.597-605

2015

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From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family

Pediatric allergy and immunology, 2012-11, Vol.23 (7), p.660-666

2012

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Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies

Molecular immunology, 2008-01, Vol.45 (2), p.479-484

2008

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Hipogammaglobulinemia crónica postrasplante de precursores hematopoyéticos y su tratamiento con gammaglobulina subcutánea en pacientes pediátricos

Anales de pediatría (Barcelona, Spain : 2003), 2022-08, Vol.97 (2), p.103-111

2022

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The polymorphism p.G219R of CD40L does not cause immunological alterations in vivo: Conclusions from a X-linked hyper IgM syndrome kindred

Molecular immunology, 2012-10, Vol.52 (3-4), p.237-241

2012

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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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Hematopoietic stem cell transplantation in patients with Gain of Function STAT1 Mutation

Journal of allergy and clinical immunology, 2017

2017

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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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Chronic hypogammaglobulinemia after allogeneic stem cell transplantation and their treatment with subcutaneous immunoglobulin in pediatric patients

Anales de Pediatría, 2022-08, Vol.97 (2), p.103-111

2022

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Non-myeloablative hematopoietic stem cell transplantation in the treatment of severe idiopathic CD4+ lymphocytopenia: Stem cell transplantation for CD4 lymphocytopenia

European journal of haematology, 2011-07, Vol.87 (1), p.87-91

2011

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Una nueva página web para todos

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

2013

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Cost-effectiveness analysis of HLA-B5701 typing in the prevention of hypersensitivity to abacavir in HIV+ patients in Spain

Enfermedades infecciosas y microbiologia clinica, 2010-11, Vol.28 (9), p.590-595

2010

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A novel mutation in the TAP2 gene in bare lymphocyte syndrome: association with metastatic cutaneous squamous cell carcinoma

Archives of dermatology (1960), 2010-01, Vol.146 (1), p.96

2010

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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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MspI polymorphism of the human p53 gene

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

1990

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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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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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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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Polymorphisms of Pyrimidine Pathway Enzymes Encoding Genes and HLA-B40∶01 Carriage in Stavudine-Associated Lipodystrophy in HIV-Infected Patients

Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations

Inherited human ezrin deficiency impairs adaptive immunity

Anti-NF155 chronic inflammatory demyelinating polyradiculoneuropathy strongly associates to HLA-DRB15

Non‐myeloablative hematopoietic stem cell transplantation in the treatment of severe idiopathic CD4+ lymphocytopenia

A novel gain-of-function STAT1 mutation resulting in basal phosphorylation of STAT1 and increased distal IFN-γ-mediated responses in chronic mucocutaneous candidiasis

Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family

Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies

Hipogammaglobulinemia crónica postrasplante de precursores hematopoyéticos y su tratamiento con gammaglobulina subcutánea en pacientes pediátricos

The polymorphism p.G219R of CD40L does not cause immunological alterations in vivo: Conclusions from a X-linked hyper IgM syndrome kindred

Hacia dónde va la Sociedad Española de Inmunología?

Hematopoietic stem cell transplantation in patients with Gain of Function STAT1 Mutation

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

Chronic hypogammaglobulinemia after allogeneic stem cell transplantation and their treatment with subcutaneous immunoglobulin in pediatric patients

Non-myeloablative hematopoietic stem cell transplantation in the treatment of severe idiopathic CD4+ lymphocytopenia: Stem cell transplantation for CD4 lymphocytopenia

Una nueva página web para todos

Cost-effectiveness analysis of HLA-B5701 typing in the prevention of hypersensitivity to abacavir in HIV+ patients in Spain

A novel mutation in the TAP2 gene in bare lymphocyte syndrome: association with metastatic cutaneous squamous cell carcinoma

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

Langerhans cell deficiency in reticular dysgenesis

MspI polymorphism of the human p53 gene

Mspl polymorphism of the human p53 gene

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

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

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