ESTELA NATIVIDAD PAZ ARTAL-rekin lankidetzan egindako argitalpenak (10)

2021

  1. Primary Immune Regulatory Disorders With an Autoimmune Lymphoproliferative Syndrome-Like Phenotype: Immunologic Evaluation, Early Diagnosis and Management

    Frontiers in Immunology, Vol. 12

2017

  1. Acquired senescent T-cell phenotype correlates with clinical severity in GATA binding protein 2-deficient patients

    Frontiers in Immunology, Vol. 8, Núm. JUL

2015

  1. Decreased activation-induced cell death by EBV-transformed B-cells from a patient with autoimmune lymphoproliferative syndrome caused by a novel FASLG mutation

    Pediatric Research, Vol. 78, Núm. 6, pp. 603-608

2014

  1. A case of partial dedicator of cytokinesis 8 deficiency with altered effector phenotype and impaired CD8+ and natural killer cell cytotoxicity

    Journal of Allergy and Clinical Immunology, Vol. 134, Núm. 1

2011

  1. Phenotypic and functional evaluation of CD3 +CD4 -CD8 -T cells in human cd8 immunodeficiency

    Haematologica, Vol. 96, Núm. 8, pp. 1195-1203

  2. Possible role of Artemis c.512C>G polymorphic variant in Omenn syndrome

    DNA Repair

2008

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

    Molecular Immunology, Vol. 45, Núm. 2, pp. 479-484

  2. Longitudinal analysis of immune function in the first 3 years of life in thymectomized neonates during cardiac surgery

    Clinical and Experimental Immunology, Vol. 154, Núm. 3, pp. 375-383

2006

  1. A homozygous Fas ligand gene mutation in a patient causes a new type of autoimmune lymphoproliferative syndrome

    Blood, Vol. 108, Núm. 4, pp. 1306-1312

2004

  1. Partial immune reconstitution after bone marrow transplantation in a boy with recombination activating gene 1 defect [5]

    Bone Marrow Transplantation