Inmunología, Oftalmología y ORL
Departamento
Necker-Enfants Malades Hospital
París, FranciaPublicaciones en colaboración con investigadores/as de Necker-Enfants Malades Hospital (27)
2024
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Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells
Science Immunology, Vol. 9, Núm. 91
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The immunopathological landscape of human pre-TCRa deficiency: From rare to common variants
Science, Vol. 383, Núm. 6686
2023
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Correction: “The 5th edition of The World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms” Leukemia. 2022 Jul;36(7):1720–1748 (Leukemia, (2022), 36, 7, (1720-1748), 10.1038/s41375-022-01620-2)
Leukemia
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NOVATIVE: A Phase II/III, Multicenter, Double-masked, Randomized Study of Cyclosporine A 0.05% and 0.1% Ophthalmic Cationic Emulsion Versus Vehicle in Patients with Vernal Keratoconjunctivitis
Clinical Therapeutics, Vol. 45, Núm. 12, pp. 1284-1288
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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
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The PID Odyssey 2030: outlooks, unmet needs, hurdles, and opportunities — proceedings from the IPOPI global multi-stakeholders’ summit (June 2022)
Frontiers in Immunology, Vol. 14
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Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs
Science immunology, Vol. 8, Núm. 90, pp. eabp8966
2022
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Human genetic and immunological determinants of critical COVID-19 pneumonia
Nature, Vol. 603, Núm. 7902, pp. 587-598
2021
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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
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Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)
European Journal of Immunology, Vol. 51, Núm. 12, pp. 2708-3145
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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
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X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19
Science immunology, Vol. 6, Núm. 62
2020
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Human BCL10 Deficiency due to Homozygosity for a Rare Allele
Journal of Clinical Immunology, Vol. 40, Núm. 2, pp. 388-398
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
2019
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Double-strand break repair through homologous recombination in autosomal-recessive BCL10 deficiency
Journal of Allergy and Clinical Immunology, Vol. 143, Núm. 5, pp. 1931-1934.e1
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Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations
Clinical Immunology, Vol. 201, pp. 30-34
2018
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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
2017
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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
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The homozygous R504C mutation in MTO1 gene is responsible for ONCE syndrome
Clinical Genetics, Vol. 91, Núm. 1, pp. 46-53