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Volumn 32, Issue 9, 2008, Pages 1483-1485

Hypereosinophilic syndrome: Another face of janus?

Author keywords

[No Author keywords available]

Indexed keywords

BCR ABL PROTEIN; CYANOCOBALAMIN; HYDROXYUREA; IMMUNOGLOBULIN E; INTERLEUKIN 12; JANUS KINASE 2; STEM CELL FACTOR; STEROID; T LYMPHOCYTE RECEPTOR GAMMA CHAIN;

EID: 43049166913     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2007.12.007     Document Type: Letter
Times cited : (8)

References (8)
  • 1
    • 0016430025 scopus 로고
    • The hypereosinophilic syndrome: analysis of fourteen cases with review of the literature
    • Chusid M.J., Dale D.C., West B.C., and Wolff S.M. The hypereosinophilic syndrome: analysis of fourteen cases with review of the literature. Medicine (Baltimore) 54 (1975) 1-27
    • (1975) Medicine (Baltimore) , vol.54 , pp. 1-27
    • Chusid, M.J.1    Dale, D.C.2    West, B.C.3    Wolff, S.M.4
  • 2
    • 33646245681 scopus 로고    scopus 로고
    • Eosinophilia: secondary, clonal and idiopathic
    • Tefferi A., Patnaik M.M., and Pardanani A. Eosinophilia: secondary, clonal and idiopathic. Br J Haematol 133 (2006) 468-492
    • (2006) Br J Haematol , vol.133 , pp. 468-492
    • Tefferi, A.1    Patnaik, M.M.2    Pardanani, A.3
  • 4
    • 0033867827 scopus 로고    scopus 로고
    • Detection of c-kit mutation Asp 816 to Val in microdissected bone marrow infiltrates in a case of systemic mastocytosis associated with chronic myelomonocytic leukaemia
    • Sotlar K., Marafioti T., Griesser H., Theil J., Aepinus C., Jaussi R., et al. Detection of c-kit mutation Asp 816 to Val in microdissected bone marrow infiltrates in a case of systemic mastocytosis associated with chronic myelomonocytic leukaemia. Mol Pathol 53 (2000) 188-193
    • (2000) Mol Pathol , vol.53 , pp. 188-193
    • Sotlar, K.1    Marafioti, T.2    Griesser, H.3    Theil, J.4    Aepinus, C.5    Jaussi, R.6
  • 5
    • 0344809973 scopus 로고    scopus 로고
    • Abnormal clones of T cells producing interleukin-5 in idiopathic eosinophilia
    • Simon H.U., Plotz S.G., Dummer R., and Blaser K. Abnormal clones of T cells producing interleukin-5 in idiopathic eosinophilia. N Engl J Med 341 (1999) 1112-1120
    • (1999) N Engl J Med , vol.341 , pp. 1112-1120
    • Simon, H.U.1    Plotz, S.G.2    Dummer, R.3    Blaser, K.4
  • 6
    • 21344467318 scopus 로고    scopus 로고
    • Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
    • Jones A.V., Kreil S., Zoi K., Waghorn K., Curtis C., Zhang L., et al. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood 106 (2005) 2162-2168
    • (2005) Blood , vol.106 , pp. 2162-2168
    • Jones, A.V.1    Kreil, S.2    Zoi, K.3    Waghorn, K.4    Curtis, C.5    Zhang, L.6
  • 7
    • 0344987881 scopus 로고    scopus 로고
    • A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
    • Cools J., DeAngelo D.J., Gotlib J., Stover E.H., Legare R.D., Cortes J., et al. A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. N Engl J Med 348 (2003) 1201-1214
    • (2003) N Engl J Med , vol.348 , pp. 1201-1214
    • Cools, J.1    DeAngelo, D.J.2    Gotlib, J.3    Stover, E.H.4    Legare, R.D.5    Cortes, J.6
  • 8
    • 21344440357 scopus 로고    scopus 로고
    • The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
    • Steensma D.P., Dewald G.W., Lasho T.L., Powell H.L., McClure R.F., Levine R.L., et al. The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes. Blood 106 (2005) 1207-1209
    • (2005) Blood , vol.106 , pp. 1207-1209
    • Steensma, D.P.1    Dewald, G.W.2    Lasho, T.L.3    Powell, H.L.4    McClure, R.F.5    Levine, R.L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.