Publicaciones en las que colabora con LUIS MIGUEL ALLENDE MARTÍNEZ (20)

2023

  1. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

    Genome Medicine, Vol. 15, Núm. 1

2022

  1. Altered CXCR4 dynamics at the cell membrane impairs directed cell migration in WHIM syndrome patients

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 119, Núm. 21

2021

  1. Clinical and Immunological Features of Human BCL10 Deficiency

    Frontiers in Immunology, Vol. 12

  2. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

    Journal of Allergy and Clinical Immunology, Vol. 148, Núm. 5, pp. 1332-1341.e5

  3. Next Generation Sequencing for Detecting Somatic FAS Mutations in Patients With Autoimmune Lymphoproliferative Syndrome

    Frontiers in Immunology, Vol. 12

2020

  1. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  2. Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies

    Journal of Allergy and Clinical Immunology: In Practice, Vol. 8, Núm. 10, pp. 3342-3347

  3. Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies

    Enfermedades Infecciosas y Microbiologia Clinica, Vol. 38, Núm. 9, pp. 438-443

  4. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

2019

  1. Extreme phenotypes with identical mutations: Two patients with same non-sense NHEJ1 homozygous mutation

    Frontiers in Immunology, Vol. 10, Núm. JAN

2018

  1. Patients with CD3G mutations reveal a role for human CD3g in Treg diversity and suppressive function

    Blood, Vol. 131, Núm. 21, pp. 2335-2344

2016

  1. Multicenter study for the evaluation of the antibody response against salmonella typhi Vi vaccination (EMPATHY) for the diagnosis of Anti-polysaccharide antibody production deficiency in patients with primary immunodeficiency

    Clinical Immunology, Vol. 169, pp. 80-84

2015

  1. γδ T lymphocytes in the diagnosis of human T cell receptor immunodeficiencies

    Frontiers in Immunology

2013

  1. Human CD3γ, but not CD3δ, haploinsufficiency differentially impairs γδ versus αβ surface TCR expression

    BMC Immunology, Vol. 14, Núm. 1

2011

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

    DNA Repair

2007

  1. Differential biological role of CD3 chains revealed by human immunodeficiencies

    Journal of Immunology, Vol. 178, Núm. 4, pp. 2556-2564

2003

  1. Toward Gene Therapy for Human CD3 Deficiencies

    Human Gene Therapy, Vol. 14, Núm. 17, pp. 1653-1661

1998

  1. Description of two Mhc-C-related sequences in the New World monkey Saguinus oedipus

    European Journal of Immunogenetics, Vol. 25, Núm. 6, pp. 409-417

1996

  1. Herpes virus saimiri transformation of T cells in CD3γ immunodeficiency: Phenotypic and functional characterization

    Journal of Immunological Methods, Vol. 198, Núm. 2, pp. 177-186

1994

  1. Peripheral blood reduction of memory (CD29+, CD45RO+, and "Bright" CD2+ and LFA-1+) T lymphocytes in Papillon-Lefèvre syndrome

    Human Immunology, Vol. 41, Núm. 3, pp. 185-192