Mutation analysis and therapeutic response to granulocyte colony-stimulating factor in a case of hyperimmunoglobulin m syndrome with chronic neutropenia

American Journal of Pediatric Hematology/Oncology

Volumn 22, Issue 3, 2000, Pages 288-289

  Mori, Masaaki ^a   Nonoyama, Shigeaki ^a   Neubauer, Michael ^a   Mitsuda, Toshihiro ^a   Kosuge, Keiji ^a   Yokota, Shumpei ^a  

^a YOKOHAMA CITY UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADRENALIN; GRANULOCYTE COLONY STIMULATING FACTOR; HYDROCORTISONE;

ADOLESCENT; BONE MARROW EXAMINATION; CASE REPORT; CHRONIC DISEASE; GENE MUTATION; HEMATOLOGIC DISEASE; HUMAN; HUMAN CELL; HYPERIMMUNOGLOBULINEMIA M; IMMUNE DEFICIENCY; LETTER; LEUKOCYTE COUNT; MALE; NEUTROPENIA; PRIORITY JOURNAL; RECURRENT INFECTION; SYNDROME DELINEATION; TREATMENT OUTCOME;

ADOLESCENT; AGAMMAGLOBULINEMIA; B-LYMPHOCYTES; CD40 LIGAND; COMMON VARIABLE IMMUNODEFICIENCY; DIAGNOSTIC ERRORS; DNA MUTATIONAL ANALYSIS; GRANULOCYTE COLONY-STIMULATING FACTOR; HUMANS; HYPERGAMMAGLOBULINEMIA; IGA DEFICIENCY; IGG DEFICIENCY; IMMUNOGLOBULIN D; IMMUNOGLOBULIN E; IMMUNOGLOBULIN M; IMMUNOGLOBULINS, INTRAVENOUS; MALE; MEMBRANE GLYCOPROTEINS; NEUTROPENIA; SEQUENCE DELETION; SYNDROME;

EID: 0034454029     PISSN: 01928562     EISSN: None     Source Type: Journal    
DOI: 10.1097/00043426-200005000-00020     Document Type: Letter

References (6)

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