Hypogammaglobulinemia with hyper-IgM, severe T-cell defect, and abnormal recirculation of OKT4 lymphocytes in a girl with chronic lymphadenopathy

Clinical Immunology and Immunopathology

Volumn 38, Issue 2, 1986, Pages 256-264

  Fiorilli, Massimo ^a   Russo, Giandomenico ^a   Paganelli, Roberto ^a   Papetti, Claudia ^a   Carbonari, Maurizio ^a   Crescenzi, Marco ^a   Calvani, Mario ^b   Quinti, Isabella ^a   Aiuti, Fernando ^a  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

^b SAN CAMILLO FORLANINI HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

OKT 4; POKEWEED MITOGEN;

B LYMPHOCYTE; EPSTEIN BARR VIRUS; GIRL; HYPOGAMMAGLOBULINEMIA; IMMUNE DEFICIENCY; LYMPHADENOPATHY; LYMPHATIC SYSTEM; PRIORITY JOURNAL; T LYMPHOCYTE;

AGAMMAGLOBULINEMIA; ANTIBODIES, MONOCLONAL; B-LYMPHOCYTES; CHILD; CHRONIC DISEASE; FEMALE; HUMANS; HYPERGAMMAGLOBULINEMIA; IMMUNOGLOBULIN M; INTERFERON TYPE II; LYMPH NODES; LYMPHOPROLIFERATIVE DISORDERS; PHENOTYPE; T-LYMPHOCYTES;

EID: 0022643294     PISSN: 00901229     EISSN: None     Source Type: Journal    
DOI: 10.1016/0090-1229(86)90143-1     Document Type: Article

References (27)

1. Severe combined immunodeficiency with quantitatively normal but abnormally differentiated T lymphocytes