Gene abnormalities in patients with hemophagocytic lymphohistiocytosis

Israel Medical Association Journal

Volumn 4, Issue 5, 2002, Pages 366-369

  Grunebaum, Eyal ^a   Roifman, Chaim M ^a  

^a SCHNEIDER CHILDREN S MEDICAL CENTER OF ISRAEL   (Israel)

Author keywords

Gene defects; Hemophagocytosis; Histiocytosis; Immunodeficiency

Indexed keywords

ENZYMES; IMMUNOLOGY; MUTAGENESIS; PATIENT MONITORING;

IMMUNE DEFICIENCY;

GENES;

INTERLEUKIN 2 RECEPTOR; PERFORIN; PURINE NUCLEOSIDE PHOSPHORYLASE;

BONE MARROW TRANSPLANTATION; CLINICAL FEATURE; DISEASE CLASSIFICATION; DISEASE SEVERITY; FAMILIAL DISEASE; GENE MUTATION; GENETIC COUNSELING; GENETIC DISORDER; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HISTIOCYTOSIS; HUMAN; IMMUNE DEFICIENCY; IMMUNE FUNCTION TEST; PATHOGENESIS; REVIEW;

CARRIER PROTEINS; HISTIOCYTOSIS, NON-LANGERHANS-CELL; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MEMBRANE GLYCOPROTEINS; MUTATION; PORE FORMING CYTOTOXIC PROTEINS; PURINE-NUCLEOSIDE PHOSPHORYLASE; RECEPTORS, INTERLEUKIN-2;

EID: 0036247180     PISSN: 15651088     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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