Perforin defects of primary haemophagocytic lymphohistiocytosis in Japan

British Journal of Haematology

Volumn 116, Issue 2, 2002, Pages 346-349

  Suga, Naohiro ^a   Takada, Hidetoshi ^a   Nomura, Akihiko ^a   Ohga, Shouichi ^a   Ishii, Eiichi ^a,b   Ihara, Kenji ^a   Ohshima, Koichi ^c   Hara, Toshiro ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b SAGA UNIVERSITY   (Japan)

^c FUKUOKA UNIVERSITY   (Japan)

Author keywords

Flow cytometry; Haemophagocytic lymphohistiocytosis; Perforin

Indexed keywords

CD56 ANTIGEN; CD8 ANTIGEN; PERFORIN;

ALLELE; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; FLOW CYTOMETRY; GENE EXPRESSION; GENE FREQUENCY; GENE MUTATION; GENETIC DISORDER; GENETIC SCREENING; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HEMOPHAGOCYTIC SYNDROME; HETEROZYGOTE; HISTIOCYTOSIS; HUMAN; JAPAN; MALE; PRIORITY JOURNAL; SIBLING; SURVIVAL; T LYMPHOCYTE;

AGE OF ONSET; ANTIGENS, CD56; ANTIGENS, CD8; FEMALE; FLOW CYTOMETRY; HETEROZYGOTE; HISTIOCYTOSIS, NON-LANGERHANS-CELL; HUMANS; INFANT; INFANT, NEWBORN; LEUKOCYTES; MALE; MEMBRANE GLYCOPROTEINS; MUTATION; PEDIGREE; PORE FORMING CYTOTOXIC PROTEINS;

EID: 0036181273     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2002.03266.x     Document Type: Article

References (12)

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2. Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity
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4. Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH)
5. Diagnostic guidelines for hemophagocytic lymphohistiocytosis
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7. Effective control of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis with immunodeficiency
8. Clinical and epidemiological studies of familial erythrophagocytic lymphohistiocytosis in Japan
9. Treatment of familial hemophagocytic lymphohistiocytosis with bone marrow transplantation from HLA genetically non-identical donors
10. Infection- and malignancy-associated hemophagocytic syndromes; secondary hemophagocytic lymphohistiocytosis
11. Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping
12. Perforin gene defects in familial hemophagocytic lymphohistiocytosis