14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator Deficiency.
Schepp, Johanna; Chou, Janet; Skrabl-Baumgartner, Andrea; Arkwright, Peter D; Engelhardt, Karin R; Hambleton, Sophie; Morio, Tomohiro; Röther, Ekkehard; Warnatz, Klaus; Geha, Raif; Grimbacher, Bodo.
; 8: 964, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28861081
Defects of B-cell terminal differentiation in patients with type-1 Kabuki syndrome.
Hypogammaglobulinémie transitoire de l'enfant.
Diagnostic and therapeutic considerations in patients with hypogammaglobulinemia after rituximab therapy.
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy.
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.
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A life of adventure in immunobiology.