Résultat(s) 1 - 15 résultats de 15 pour la requête 'Gazzurelli, Luisa', Temps de recherche: 2,00s Affiner les résultats
  1. 1
    Clinical and immunological analysis of a large kindred affected by autoimmune lymphoproliferative syndrome (ALPS) due to a novel TNFRSF6 mutation displaying age dependent disease activity
    Autres auteurs: “...Gazzurelli, Luisa...”

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  2. 2
    Lymphocyte alterations in patients with Common Variable Immunodeficiency (CVID) and autoimmune manifestations
    Autres auteurs: “...Gazzurelli, Luisa...”

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  3. 3
    Lack of DOCK8 impairs the primary biologic functions of human NK cells and abrogates CCR7 surface expression in a WASP-independent manner
    Autres auteurs: “...Gazzurelli, Luisa...”

    Article en ligne

  4. 4
    Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS)
    Autres auteurs: “...Gazzurelli, Luisa...”

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  5. 5
    Fatal SARS-CoV-2 infection in a male patient with Good's syndrome
    Autres auteurs: “...Gazzurelli, Luisa...”

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  6. 6
    Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion
    Autres auteurs: “...Gazzurelli, Luisa...”

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  7. 7
    Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ
    Autres auteurs: “...Gazzurelli, Luisa...”

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  8. 8
    NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential
    Autres auteurs: “...Gazzurelli, Luisa...”

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  9. 9
    Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity
    Autres auteurs: “...Gazzurelli, Luisa...”

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  10. 10
    The RAC2-PI3K axis regulates human NK cell maturation and function
    Autres auteurs: “...Gazzurelli, Luisa...”

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  11. 11
    A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1)
    Autres auteurs: “...Gazzurelli, Luisa...”

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  12. 12
    CTLA-4 regulates human Natural Killer cell effector functions
    Autres auteurs: “...Gazzurelli, Luisa...”

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  13. 13
    Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay
    Autres auteurs: “...Gazzurelli, Luisa...”

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  14. 14
    Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency
    Autres auteurs: “...Gazzurelli, Luisa...”

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  15. 15
    A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy
    Autres auteurs: “...Gazzurelli, Luisa...”

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