A primary immunodeficiency disorder associated with absence of lymphoid germinal centers

Journal of Clinical Immunology

Volumn 22, Issue 5, 2002, Pages 297-305

  Eisenstein, Eli M ^a   Aker, Memet ^a   Savoldi, Gianfranco ^b   Jaffe, Ronald ^c   Prus, Diana ^a  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^b Instituto di Medicina Molecolare Angelo Novicelli Spediali Civili   (Italy)

^c CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

Author keywords

Agammaglobulinemia; Dendritic cell; Germinal center; Hyper IgM syndrome; Tumor necrosis factor superfamily

Indexed keywords

TUMOR NECROSIS FACTOR;

AGAMMAGLOBULINEMIA; ARTICLE; CASE REPORT; CLINICAL FEATURE; DENDRITIC CELL; DNA SEQUENCE; FEMALE; GENETIC VARIABILITY; GERMINAL CENTER; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERIMMUNOGLOBULINEMIA M; IMMUNE DEFICIENCY; IMMUNOHISTOCHEMISTRY; INFANT; INTESTINE; LYMPHOCYTE COUNT; LYMPHOCYTE PROLIFERATION; LYMPHOCYTE SUBPOPULATION; LYMPHOID TISSUE; MALE; PLASMA CELL; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

AGAMMAGLOBULINEMIA; ANTIGENS, CD; ANTIGENS, CD40; ANTIGENS, DIFFERENTIATION, B-LYMPHOCYTE; BIOLOGICAL MARKERS; CELL CULTURE TECHNIQUES; DENDRITIC CELLS; FEMALE; GERMINAL CENTER; HUMANS; HYPERGAMMAGLOBULINEMIA; IMMUNOGLOBULIN M; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT; LYMPHOID TISSUE; MALE; T-LYMPHOCYTES;

EID: 0036747816     PISSN: 02719142     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1019978122881     Document Type: Article

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