Publicaciones en colaboración con investigadores/as de Necker-Enfants Malades Hospital (13)

2024

  1. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children

    The Journal of experimental medicine, Vol. 221, Núm. 2

  2. Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells

    Science Immunology, Vol. 9, Núm. 91

2023

  1. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

    Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 4, pp. 984-996.e10

  2. 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. Autoantibodies against type I IFNs in patients with critical influenza pneumonia

    The Journal of experimental medicine, Vol. 219, Núm. 11

2021

  1. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

    Journal of Allergy and Clinical Immunology, Vol. 147, Núm. 2, pp. 520-531

  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

2019

  1. Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations

    Clinical Immunology, Vol. 201, pp. 30-34

2018

  1. Disseminated abscesses due to Mycoplasma faucium in a patient with activated PI3Kδ syndrome type 2

    Journal of Allergy and Clinical Immunology: In Practice, Vol. 6, Núm. 5, pp. 1796-1798.e2

  2. Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders

    Journal of Allergy and Clinical Immunology, Vol. 141, Núm. 1, pp. 322-328.e10

2017

  1. A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis

    Journal of Allergy and Clinical Immunology, Vol. 139, Núm. 4, pp. 1302-1310.e4

2015

  1. DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

    Journal of Clinical Immunology, Vol. 35, Núm. 2, pp. 189-198

  2. The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: Implications for differential diagnosis and pathogenesis

    Haematologica, Vol. 100, Núm. 7, pp. 978-988