Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome

D. Montin, A. Marolda, F. Licciardi, F. Robasto, S. Di Cesare, E. Ricotti, F. Ferro, G. Scaioli, C. Giancotta, D. Amodio, F. Conti, G. Giardino, L. Leonardi, S. Ricci, S. Volpi, L.A. Baselli, C. Azzari, G. Bossi, R. Consolini, R.M. DellepianeM. Duse, M. Gattorno, B. Martire, M.C. Putti, A. Soresina, A. Plebani, U. Ramenghi, S. Martino, C. Pignata, C. Cancrini

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)2369-2376
JournalJournal of Allergy and Clinical Immunology: In Practice
Volume7
Issue number7
DOIs
Publication statusPublished - 2019

Keywords

  • 22q11.2 deletion syndrome
  • Autoimmune cytopenia
  • B immunophenotype
  • CD4 naïve cells
  • DiGeorge syndrome
  • Hemolytic anemia
  • NK cells
  • Switched memory B cells
  • T immunophenotype
  • Thrombocytopenic purpura

Cite this