Résultat(s) 1 - 11 résultats de 11 pour la requête 'Imai, Kohsuke', Temps de recherche: 1,34s Affiner les résultats
  1. 1
    JAK inhibitor ameliorates inflammatory bowel disease in a patient with IKZF1 haploinsufficiency
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  2. 2
    Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  3. 3
    Immunophenotyping of A20 haploinsufficiency by multicolor flow cytometry
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  4. 4
    Identification of autoantibodies using human proteome microarrays in patients with IPEX syndrome
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  5. 5
    A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM)
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  6. 6
    High frequencies of asymptomatic Epstein-Barr virus viremia in affected and unaffected individuals with CTLA4 mutations
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  7. 7
    Clinical and molecular features of X-linked hyper IgM syndrome - An experience from North India
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  8. 8
    Maternal T and B cell engraftment in two cases of X-linked severe combined immunodeficiency with IgG1 gammopathy
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  9. 9
    Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  10. 10
    Analysis of mutations and recombination activity in RAG-deficient patients
    Autres auteurs: “...Imai, Kohsuke...”

    Article en ligne

  11. 11
    Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2
    Article

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