O. de la Calle‐Martín

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

A. Martín-Nalda, L. Alsina, I. Badell, 2012, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

T. Morio, H. Ochs, T. Torgerson, 2017, The Journal of allergy and clinical immunology.

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

E. Campo, R. Miquel, A. Palacín, 1991, Cancer research.

Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases

J. Yagüe, C. Wouters, E. López-Granados, 2019, The Journal of allergy and clinical immunology.

AccII polymorphism of the p53 gene.

J. Yagüe, J. Vives, V. Fabregat, 1990, Nucleic acids research.

MspI polymorphism of the human p53 gene.

J. Yagüe, G. Ercilla, J. Vives, 1990, Nucleic acids research.

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

Antonio Martínez, Felipe García, J. Gatell, 2011, European journal of haematology.

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

A. España, C. González-Santesteban, L. Martínez-Martínez, 2010, Archives of dermatology.

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

P. Fuentes-Prior, C. Rodríguez-Gallego, I. Badell, 2015, Molecular immunology.

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

J. Rodríguez-Sánchez, I. Badell, N. Casamitjana, 1997, Clinical and experimental immunology.

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

T. Gallart, J. Alberola-Ila, P. Engel, 1992, European journal of immunology.

The V beta 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

P. Kourilsky, J. Abastado, B. Malissen, 1994, The Journal of experimental medicine.

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

J. Cigudosa, M. Bofill, J. Rodríguez-Sánchez, 2008, European Respiratory Journal.

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

J. Yagüe, M. Plana, R. Vilella, 1991, European journal of immunology.

Polymorphisms of Pyrimidine Pathway Enzymes Encoding Genes and HLA-B*40∶01 Carriage in Stavudine-Associated Lipodystrophy in HIV-Infected Patients

F. Villarroya, M. Baiget, F. Vidal, 2013, PloS one.

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

I. Caragol, J. Rodríguez-Sánchez, J. Ordi, 2001, The Journal of clinical investigation.

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

I. Badell, C. González-Santesteban, L. Martínez-Martínez, 2012, Molecular immunology.

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

J. Bertranpetit, E. Coto, L. Kalaydjieva, 2008, Molecular immunology.

Familial CD8 deficiency due to a mutation in the CD8α gene

I. Caragol, J. Rodríguez-Sánchez, J. Ordi, 2001 .

Inherited human ezrin deficiency impairs adaptive immunity.

J. Casanova, S. Sánchez-Ramón, R. Mena, 2023, The Journal of allergy and clinical immunology.