Résultat(s) 1 - 9 résultats de 9 pour la requête 'Hammarstrom, Lennart', Temps de recherche: 1,87s Affiner les résultats
  1. 1
    Study of an extended family with CTLA-4 deficiency suggests a CD28/CTLA-4 independent mechanism responsible for differences in disease manifestations and severity
    Autres auteurs: “...Hammarström, Lennart...”

    Article en ligne

  2. 2
    Defective TLR9-driven STAT3 activation in B cells of patients with CVID
    Autres auteurs: “...Hammarstrom, Lennart...”

    Article en ligne

  3. 3
    NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion
    Autres auteurs: “...Hammarström, Lennart...”

    Article en ligne

  4. 4
    Novel NLRP12 mutations associated with intestinal amyloidosis in a patient diagnosed with common variable immunodeficiency
    Autres auteurs: “...Hammarström, Lennart...”

    Article en ligne

  5. 5
    Newborn screening for severe T and B cell lymphopenia identifies a fraction of patients with Wiskott-Aldrich syndrome
    Autres auteurs: “...Hammarström, Lennart...”

    Article en ligne

  6. 6
    Familial aggregation of IgAD and autoimmunity
    Autres auteurs: “...Hammarstrom, Lennart...”

    Article en ligne

  7. 7
    Selective IgA deficiency in early life association to infections and allergic diseases during childhood
    Autres auteurs: “...Hammarström, Lennart...”

    Article en ligne

  8. 8
    Restricted immunoglobulin constant heavy G chain genes in primary immunodeficiencies
    Autres auteurs: “...Hammarström, Lennart...”

    Article en ligne

  9. 9
    ICOS deficiency in patients with common variable immunodeficiency
    Autres auteurs: “...Hammarstrom, Lennart...”
    Article

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