메뉴 건너뛰기




Volumn 51, Issue 4, 2009, Pages 371-374

Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation

Author keywords

Child; Epstein Barr virus; Familial hemophagocytic lymphohistiocytosis; Syntaxin 11 mutation

Indexed keywords

ACICLOVIR; ALANINE AMINOTRANSFERASE; ANTIBIOTIC AGENT; ASPARTATE AMINOTRANSFERASE; CYCLOSPORIN A; IMMUNOGLOBULIN; MEMBRANE PROTEIN; PERFORIN; PROTEIN MUNC13 4; SYNTAXIN; SYNTAXIN 11; TRIACYLGLYCEROL; UNCLASSIFIED DRUG;

EID: 70649090277     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (18)
  • 1
    • 33845878531 scopus 로고    scopus 로고
    • Familial and acquired hemophagocytic lymphohistiocytosis
    • Janka GE. Familial and acquired hemophagocytic lymphohistiocytosis. Eur J Pediatr 2007; 166: 95-109.
    • (2007) Eur J Pediatr , vol.166 , pp. 95-109
    • Janka, G.E.1
  • 3
    • 20144363940 scopus 로고    scopus 로고
    • Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type- 4 to chromosome 6q24 and identification of mutations in syntaxin 11
    • zur Stadt U, Schmidt S, Kasper B, et al. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type- 4 to chromosome 6q24 and identification of mutations in syntaxin 11. Hum Mol Genet 2005; 14: 827-834.
    • (2005) Hum Mol Genet , vol.14 , pp. 827-834
    • Zur Stadt, U.1    Schmidt, S.2    Kasper, B.3
  • 4
    • 40849097696 scopus 로고    scopus 로고
    • Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations
    • Okur H, Balta G, Akarsu N, et al. Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations. Leuk Res 2008; 32: 972-975.
    • (2008) Leuk Res , vol.32 , pp. 972-975
    • Okur, H.1    Balta, G.2    Akarsu, N.3
  • 6
    • 33745052933 scopus 로고    scopus 로고
    • Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: Association with disease-free remissions and haematopoietic malignancies
    • Rudd E, Grönsdotter Ericson K, Zheng C, et al. Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies. J Med Genet 2006; 43: e14.
    • (2006) J Med Genet , vol.43
    • Rudd, E.1    Grönsdotter Ericson, K.2    Zheng, C.3
  • 8
    • 21744452702 scopus 로고    scopus 로고
    • Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome
    • Villanueva J, Lee S, Giannini EH, et al. Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome. Arthritis Res Ther 2005; 7: R30-37.
    • (2005) Arthritis Res Ther , vol.7
    • Villanueva, J.1    Lee, S.2    Giannini, E.H.3
  • 11
    • 0036786375 scopus 로고    scopus 로고
    • Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation
    • Henter JI, Samuelsson-Horne A, Arico M, et al. Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation. Blood 2002; 100: 2367-2373.
    • (2002) Blood , vol.100 , pp. 2367-2373
    • Henter, J.I.1    Samuelsson-Horne, A.2    Arico, M.3
  • 12
    • 34548814973 scopus 로고    scopus 로고
    • Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients
    • Bryceson YT, Rudd E, Zheng C, et al. Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients. Blood 2007; 110: 1906-1915.
    • (2007) Blood , vol.110 , pp. 1906-1915
    • Bryceson, Y.T.1    Rudd, E.2    Zheng, C.3
  • 13
    • 29944442846 scopus 로고    scopus 로고
    • Mutation. Spectrum in children with primary hemophagocytic lymphohistiocytosis: Molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A
    • DOI 10.1002/humu.20274
    • Zur Stadt U, Beutel K, Kolberg S, et al. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A. Hum Mut 2006; 27: 62-68. (Pubitemid 43042967)
    • (2006) Human Mutation , vol.27 , Issue.1 , pp. 62-68
    • Zur Stadt, U.1    Beutel, K.2    Kolberg, S.3    Schneppenheim, R.4    Kabisch, H.5    Janka, G.6    Hennies, H.C.7
  • 14
    • 38349146702 scopus 로고    scopus 로고
    • Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations
    • Histiocyte Society HLH Study Group
    • Trizzino A, zur Stadt U, Ueda I, Histiocyte Society HLH Study Group. Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. J Med Genet 2008; 45: 15-21.
    • (2008) J Med Genet , vol.45 , pp. 15-21
    • Trizzino, A.1    Zur Stadt, U.2    Ueda, I.3
  • 15
    • 0035889455 scopus 로고    scopus 로고
    • The role of infections in primary hemophagocytic lymphohistiocytosis: A case series and review of the literature
    • DOI 10.1086/323675
    • Sung L, Weitzman SS, Petric M, King SM. The role of infections in primary hemophagocytic lymphohistiocytosis: a case series and review of the literature. Clin Infect Dis 2001; 33: 1644-1648. (Pubitemid 33044527)
    • (2001) Clinical Infectious Diseases , vol.33 , Issue.10 , pp. 1644-1648
    • Sung, L.1    Weitzman, S.S.2    Petric, M.3    King, S.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.