메뉴 건너뛰기




Volumn 122, Issue 2, 2003, Pages 173-179

Cytogenetic and molecular genetic aspects of eosinophilic leukaemias

Author keywords

Cytogenetics; Eosinophilic leukaemia; Idiopathic hypereosinophilic syndrome; Imatinib; Molecular genetics; Oncogenes

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 1; IMATINIB; PLATELET DERIVED GROWTH FACTOR ALPHA RECEPTOR; PLATELET DERIVED GROWTH FACTOR BETA RECEPTOR;

EID: 0038487039     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2003.04458.x     Document Type: Review
Times cited : (60)

References (75)
  • 1
    • 0036207157 scopus 로고    scopus 로고
    • A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia
    • Al-Obaidi, M.J., Rymes, N., White, P., Pomfret, M., Smith, H., Starczynski, J. & Johnson, R. (2002) A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia. Acta Haematologica, 107, 98-100.
    • (2002) Acta Haematologica , vol.107 , pp. 98-100
    • Al-Obaidi, M.J.1    Rymes, N.2    White, P.3    Pomfret, M.4    Smith, H.5    Starczynski, J.6    Johnson, R.7
  • 3
    • 0036063077 scopus 로고    scopus 로고
    • Response of idiopathic hypereosinophilic syndrome to treatment with imatinib mesylate
    • Ault, O., Cortes, J., Koller, C., Kaled, E.S. & Kantarjian, H. (2002) Response of idiopathic hypereosinophilic syndrome to treatment with imatinib mesylate. Leukemia Research, 26, 881-884.
    • (2002) Leukemia Research , vol.26 , pp. 881-884
    • Ault, O.1    Cortes, J.2    Koller, C.3    Kaled, E.S.4    Kantarjian, H.5
  • 4
    • 0036211166 scopus 로고    scopus 로고
    • An overview of translocation-associated oncogenesis in the chronic myeloid leukaemias
    • Bain, B.J. (2002) An overview of translocation-associated oncogenesis in the chronic myeloid leukaemias. Acta Haematologica, 107, 57-63.
    • (2002) Acta Haematologica , vol.107 , pp. 57-63
    • Bain, B.J.1
  • 7
    • 0033935818 scopus 로고    scopus 로고
    • Cytogenetic and molecular cytogenetic characterization of 6 new cases of idiopathic hypereosinophilic syndrome
    • Bigoni, R., Cuneo, A., Roberti, M.G., Milani, R., Bardi, A., Cavazzini, F., Minotto. C. & Castoldi, G. (2000) Cytogenetic and molecular cytogenetic characterization of 6 new cases of idiopathic hypereosinophilic syndrome. Haematologica, 85, 486-491.
    • (2000) Haematologica , vol.85 , pp. 486-491
    • Bigoni, R.1    Cuneo, A.2    Roberti, M.G.3    Milani, R.4    Bardi, A.5    Cavazzini, F.6    Minotto, C.7    Castoldi, G.8
  • 8
    • 0017762355 scopus 로고
    • Chromosomal aneuploidy in a patient with hypereosinophilic syndrome: Evidence for a malignant disease
    • Bitran, J.D., Rowley, J.D., Plapp, F., Golomb, H.M. & Ultmann, J.E. (1977) Chromosomal aneuploidy in a patient with hypereosinophilic syndrome: evidence for a malignant disease. American Journal of Medicine, 68, 1010-1014.
    • (1977) American Journal of Medicine , vol.68 , pp. 1010-1014
    • Bitran, J.D.1    Rowley, J.D.2    Plapp, F.3    Golomb, H.M.4    Ultmann, J.E.5
  • 10
    • 4244108843 scopus 로고    scopus 로고
    • Eosinophilic myelodysplastic syndrome: An entity to be distinguished from the idiopathic hypereosinophilic syndrome
    • Britobabapulle, F., Butler, T.A., Secker-Walker, L. & Goldman, J.M. (1997) Eosinophilic myelodysplastic syndrome: an entity to be distinguished from the idiopathic hypereosinophilic syndrome. Blood, 90. 285b.
    • (1997) Blood , vol.90
    • Britobabapulle, F.1    Butler, T.A.2    Secker-Walker, L.3    Goldman, J.M.4
  • 11
    • 0018326169 scopus 로고
    • Chromosomal anomaly in eosinophilic leukemia
    • Cabrol, C. (1979) Chromosomal anomaly in eosinophilic leukemia. New England Journal of Medicine, 301, 439.
    • (1979) New England Journal of Medicine , vol.301 , pp. 439
    • Cabrol, C.1
  • 12
    • 0028009844 scopus 로고
    • A case of Philadelphia-negative M-BCR rearranged eosinophilic leukaemia with trisomy 8 localized by in situ hybridization
    • Chan, L.C., Kwong, Y.L., Lie, A.K.W. & Ching, L.M. (1994) A case of Philadelphia-negative M-BCR rearranged eosinophilic leukaemia with trisomy 8 localized by in situ hybridization. Leukemia, 8, 195-198.
    • (1994) Leukemia , vol.8 , pp. 195-198
    • Chan, L.C.1    Kwong, Y.L.2    Lie, A.K.W.3    Ching, L.M.4
  • 15
    • 0023205031 scopus 로고
    • A myeloproliferative disease in two infants associated with eosinophilia and a chromosome t(1;5) translocation
    • Darbyshire, P.J., Shortland, D. & Swansbury, G.J. (1987) A myeloproliferative disease in two infants associated with eosinophilia and a chromosome t(1;5) translocation. British Journal of Haematology, 66, 483-486.
    • (1987) British Journal of Haematology , vol.66 , pp. 483-486
    • Darbyshire, P.J.1    Shortland, D.2    Swansbury, G.J.3
  • 17
    • 0018647096 scopus 로고
    • Eosinophilia, chloromas and a chromosome abnormality in a patient with a myeloproliferative syndrome
    • Ellman, L., Hammond, D. & Atkins, L. (1979) Eosinophilia, chloromas and a chromosome abnormality in a patient with a myeloproliferative syndrome. Cancer, 43, 2410-2413.
    • (1979) Cancer , vol.43 , pp. 2410-2413
    • Ellman, L.1    Hammond, D.2    Atkins, L.3
  • 18
    • 0035159831 scopus 로고    scopus 로고
    • Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: The first fusion gene with BCR but not ABL
    • Fioretos, T., Panagopoulos, J., Larsen, C., Swedin, A., Billström, R., Isaksson, M., Strömbeck, B., Olofsson, T., Mitelman, F. & Johansson, B. (2001) Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene with BCR but not ABL. Genes, Chromosomes and Cancer, 32, 302-310.
    • (2001) Genes, Chromosomes and Cancer , vol.32 , pp. 302-310
    • Fioretos, T.1    Panagopoulos, J.2    Larsen, C.3    Swedin, A.4    Billström, R.5    Isaksson, M.6    Strömbeck, B.7    Olofsson, T.8    Mitelman, F.9    Johansson, B.10
  • 19
    • 18744423188 scopus 로고    scopus 로고
    • Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): Confirmation of eosinophil clonal Evolvement by fluorescence in situ hybridization
    • Forrest, D.L., Horsman, D.E., Jensen, C.L., Berry, B.R., Dalal, B.I., Barnett, M.J. & Nantel, S.H. (1998) Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal Evolvement by fluorescence in situ hybridization. Cancer Genetics and Cytogenetics, 107, 65-68.
    • (1998) Cancer Genetics and Cytogenetics , vol.107 , pp. 65-68
    • Forrest, D.L.1    Horsman, D.E.2    Jensen, C.L.3    Berry, B.R.4    Dalal, B.I.5    Barnett, M.J.6    Nantel, S.H.7
  • 22
    • 0021964479 scopus 로고
    • Is hypereosinophilic syndrome a malignant disease?
    • Gohć, K.O., Ho, F.S., Tso, S.C. & Ma, J. (1985) Is hypereosinophilic syndrome a malignant disease? Cancer, 55, 2395-2399.
    • (1985) Cancer , vol.55 , pp. 2395-2399
    • Gohć, K.O.1    Ho, F.S.2    Tso, S.C.3    Ma, J.4
  • 23
    • 0016793535 scopus 로고
    • Agar culture and chromosome analysis in eosinophilic leukaemia
    • Goldman, J.M., Najfeld, V. & Th'ng, K.H. (1975) Agar culture and chromosome analysis in eosinophilic leukaemia. Journal of Clinical Pathology, 28, 956-961.
    • (1975) Journal of Clinical Pathology , vol.28 , pp. 956-961
    • Goldman, J.M.1    Najfeld, V.2    Th'ng, K.H.3
  • 24
    • 0000433181 scopus 로고
    • Eosinophilic leukemia with chromosomal aberration t(5;12)(q31;q13): An evidence of the existence of chronic eosinophilic leukemia as a distinct myeloproliferative entity
    • Gotić, M., Radošević-Radojković, N., Ludoški, M., Spasic, P., Basara, N., Avramović, D., Bosković, D. & Rolović. Z. (1994) Eosinophilic leukemia with chromosomal aberration t(5;12)(q31;q13): an evidence of the existence of chronic eosinophilic leukemia as a distinct myeloproliferative entity. British Journal of Haematology, 87, 168.
    • (1994) British Journal of Haematology , vol.87 , pp. 168
    • Gotić, M.1    Radošević-Radojković, N.2    Ludoški, M.3    Spasic, P.4    Basara, N.5    Avramović, D.6    Bosković, D.7    Rolović, Z.8
  • 25
    • 0037973475 scopus 로고    scopus 로고
    • Imatinib mesylate (Gleevec™) induces rapid and complete hematologic remissions in patients with idiopathic hypereosinophilic syndrome (HES) without evidence of BCR-ABL or activating mutations in C-KIT and platelet-derived growth factor receptor-beta (PDGFRβ)
    • Gotlib, J., Malone, J.M., DeAngelo, D.J., Stone, R.M., Gilliland, D.G., Clark, J., Tefferi, A., Alam, R., Schrier, S.L. & Coutre, S.E. (2002) Imatinib mesylate (Gleevec™) induces rapid and complete hematologic remissions in patients with idiopathic hypereosinophilic syndrome (HES) without evidence of BCR-ABL or activating mutations in C-KIT and platelet-derived growth factor receptor-beta (PDGFRβ). Blood, 100, 798a.
    • (2002) Blood , vol.100
    • Gotlib, J.1    Malone, J.M.2    DeAngelo, D.J.3    Stone, R.M.4    Gilliland, D.G.5    Clark, J.6    Tefferi, A.7    Alam, R.8    Schrier, S.L.9    Coutre, S.E.10
  • 27
    • 18344395028 scopus 로고    scopus 로고
    • Chronic eosinophilic leukaemia presenting with erythroderma, mild eosinophilia and hyper-IgE; clinical, immunological and cytogenetic features and therapeutic approach: A case report
    • Granjo, E., Lima, M., Lopes, J.M., Dória, S., Orfâo, A., Ying, S., Barata, L.T., Miranda, M., Cross, N.C.P. & Bain, B.J. (2002) Chronic eosinophilic leukaemia presenting with erythroderma. mild eosinophilia and hyper-IgE; clinical, immunological and cytogenetic features and therapeutic approach: a case report. Acta Haematologica, 107, 108-112.
    • (2002) Acta Haematologica , vol.107 , pp. 108-112
    • Granjo, E.1    Lima, M.2    Lopes, J.M.3    Dória, S.4    Orfâo, A.5    Ying, S.6    Barata, L.T.7    Miranda, M.8    Cross, N.C.P.9    Bain, B.J.10
  • 28
    • 0036098784 scopus 로고    scopus 로고
    • Receptor tyrosine kinase mutations in myeloid neoplasms
    • Gupta, R., Knight, C. & Bain, B.J. (2002) Receptor tyrosine kinase mutations in myeloid neoplasms. British Journal of Haematology, 117, 489-508.
    • (2002) British Journal of Haematology , vol.117 , pp. 489-508
    • Gupta, R.1    Knight, C.2    Bain, B.J.3
  • 29
    • 0025351106 scopus 로고
    • Cytogenetic peculiarities in chronic myelogenous leukemia
    • Hild, F. & Fonatsch, C. (1990) Cytogenetic peculiarities in chronic myelogenous leukemia, Cancer Genetics and Cytogenetics, 47, 197-217.
    • (1990) Cancer Genetics and Cytogenetics , vol.47 , pp. 197-217
    • Hild, F.1    Fonatsch, C.2
  • 30
    • 0018642513 scopus 로고
    • Chromosomes and causation of human cancer and leukemia. XXXIV. A case of 'hypereosinophilic syndrome' with unusual cytogenetic findings in a chloroma, terminating in blastic transformation and CNS leukemia
    • Huang, C.S., Gomez, G.A., Kohno, S.I., Sokal, J.E. & Sandberg, A.A. (1979) Chromosomes and causation of human cancer and leukemia. XXXIV. A case of 'hypereosinophilic syndrome' with unusual cytogenetic findings in a chloroma, terminating in blastic transformation and CNS leukemia. Cancer, 44, 1284-1289.
    • (1979) Cancer , vol.44 , pp. 1284-1289
    • Huang, C.S.1    Gomez, G.A.2    Kohno, S.I.3    Sokal, J.E.4    Sandberg, A.A.5
  • 31
    • 0019466036 scopus 로고
    • Hypereosinophilia in a monosomy 7 myeloproliferative disorder in childhood
    • Humphrey, M.J., Hutter, J.J. & Tom, W.W. (1981) Hypereosinophilia in a monosomy 7 myeloproliferative disorder in childhood. American Journal of Hematology, 11, 107-110.
    • (1981) American Journal of Hematology , vol.11 , pp. 107-110
    • Humphrey, M.J.1    Hutter, J.J.2    Tom, W.W.3
  • 33
    • 0028237102 scopus 로고
    • A case of myelodysplasia with eosinophilia having a translocation t(5;12) (q31;q13)
    • Jani, K., Kempski, H.M. & Reeves, B.R. (1994) A case of myelodysplasia with eosinophilia having a translocation t(5;12) (q31;q13). British Journal of Haematology, 87, 57-60.
    • (1994) British Journal of Haematology , vol.87 , pp. 57-60
    • Jani, K.1    Kempski, H.M.2    Reeves, B.R.3
  • 35
    • 0013939266 scopus 로고
    • Cytogenetic studies in the chronic myeloproliferative syndrome
    • Kiossoglou, K.A., Mitus, W.J. & Dameshek, W. (1966) Cytogenetic studies in the chronic myeloproliferative syndrome. Blood, 28, 241-252.
    • (1966) Blood , vol.28 , pp. 241-252
    • Kiossoglou, K.A.1    Mitus, W.J.2    Dameshek, W.3
  • 37
    • 4243496913 scopus 로고    scopus 로고
    • Chronic eosinophilic leukemia with unique chromosomal abnormality, add(8)(p23), in a 14-month girl: Treatment with imatinib mesylate
    • Kook, H., Cho, D., Noh, H.-Y., Kim, S.-Y., Kim, H.-J., Choi, I.-S., Ryang, D.-W., Ma. J.S. & Hwang, T.J. (2002) Chronic eosinophilic leukemia with unique chromosomal abnormality. add(8)(p23), in a 14-month girl: treatment with imatinib mesylate. Blood, 100, 344b.
    • (2002) Blood , vol.100
    • Kook, H.1    Cho, D.2    Noh, H.-Y.3    Kim, S.-Y.4    Kim, H.-J.5    Choi, I.-S.6    Ryang, D.-W.7    Ma, J.S.8    Hwang, T.J.9
  • 39
    • 0018637403 scopus 로고
    • Isochromosome 17 in a patient with a myeloproliferative disorder terminating in eosinophilic leukemia
    • Lönnqvist, B., Gahrton, G., Erikson, P., Friberg, K. & Zech, L. (1979) Isochromosome 17 in a patient with a myeloproliferative disorder terminating in eosinophilic leukemia. Acta Medica Scandinavica, 206, 321-325.
    • (1979) Acta Medica Scandinavica , vol.206 , pp. 321-325
    • Lönnqvist, B.1    Gahrton, G.2    Erikson, P.3    Friberg, K.4    Zech, L.5
  • 40
    • 0032588237 scopus 로고    scopus 로고
    • αIFN-induced hematologic and cytogenetic remission in chronic eosinophilic leukemia with t(1;5)
    • Luciano, L., Catalano, L., Sarrantonio, C., Guerriero, A., Califano, C. & Rotoli, B. (1999) αIFN-induced hematologic and cytogenetic remission in chronic eosinophilic leukemia with t(1;5). Haematologica, 84, 651-653.
    • (1999) Haematologica , vol.84 , pp. 651-653
    • Luciano, L.1    Catalano, L.2    Sarrantonio, C.3    Guerriero, A.4    Califano, C.5    Rotoli, B.6
  • 41
    • 0029020637 scopus 로고
    • Refractory cytopenia with t(1;7),+8 abnormality and dysplastic eosmophils showing intranuclear Charcot-Leyden crystals: A fluorescence in situ hybridization study
    • Ma, S.K., Wong, K.F., Chan, J.K. & Kwong, Y.L. (1995) Refractory cytopenia with t(1;7),+8 abnormality and dysplastic eosmophils showing intranuclear Charcot-Leyden crystals: a fluorescence in situ hybridization study. British Journal of Haematology, 90, 216-218.
    • (1995) British Journal of Haematology , vol.90 , pp. 216-218
    • Ma, S.K.1    Wong, K.F.2    Chan, J.K.3    Kwong, Y.L.4
  • 42
    • 0036202064 scopus 로고    scopus 로고
    • The 8p11 myeloproliferative syndrome: A distinct clinical entity caused by constitutive activation of FGFR1
    • Macdonald, D., Reiter, A. & Cross, N.C.P. (2002) The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1. Acta Haematologica, 107, 101-112.
    • (2002) Acta Haematologica , vol.107 , pp. 101-112
    • Macdonald, D.1    Reiter, A.2    Cross, N.C.P.3
  • 43
    • 0003266350 scopus 로고    scopus 로고
    • Rabaptin-5, a novel fusion partner to platelet-derived growth factor beta receptor in chronic myelomonocytic leukemia
    • Magnusson, M.K., Brown, K.E., Krueger, L.A., Arthur, D.C., Barrett, J. & Dunbar, K.E. (2000) Rabaptin-5, a novel fusion partner to platelet-derived growth factor beta receptor in chronic myelomonocytic leukemia. Blood, 96, 692a.
    • (2000) Blood , vol.96
    • Magnusson, M.K.1    Brown, K.E.2    Krueger, L.A.3    Arthur, D.C.4    Barrett, J.5    Dunbar, K.E.6
  • 44
    • 0030030224 scopus 로고    scopus 로고
    • Further evidence for the clonal nature of the idiopathic hypereosinophilic syndromes: Complete haematological and cytogenetic remission induced by interferon-alpha in a case with a unique chromosomal abnormality
    • Malbrain, M.L.N.G., van den Berghe, H. & Zachée, P. (1996) Further evidence for the clonal nature of the idiopathic hypereosinophilic syndromes: complete haematological and cytogenetic remission induced by interferon-alpha in a case with a unique chromosomal abnormality. British Journal of Haematology, 92, 176-183.
    • (1996) British Journal of Haematology , vol.92 , pp. 176-183
    • Malbrain, M.L.N.G.1    Van Den Berghe, H.2    Zachée, P.3
  • 45
    • 0020512283 scopus 로고
    • Eosinophilic blast crisis in a case of chronic myeloid leukaemia
    • Marinone, G., Rossi. G. & Verzura, P. (1983) Eosinophilic blast crisis in a case of chronic myeloid leukaemia. British Journal of Haematology, 55, 251-256.
    • (1983) British Journal of Haematology , vol.55 , pp. 251-256
    • Marinone, G.1    Rossi, G.2    Verzura, P.3
  • 47
    • 0016736449 scopus 로고
    • Isochromosome 17 in a case of eosinophilic leukaemia. An abnormality common to eosinophilic and neutrophilic cells
    • Mitelman, F., Panani, A. & Brandt, L. (1975) Isochromosome 17 in a case of eosinophilic leukaemia. An abnormality common to eosinophilic and neutrophilic cells. Scandinavian Journal of Haematology, 14, 308-312.
    • (1975) Scandinavian Journal of Haematology , vol.14 , pp. 308-312
    • Mitelman, F.1    Panani, A.2    Brandt, L.3
  • 48
    • 0023198586 scopus 로고
    • Unusual chromosome 7 aberrations in a case of eosinophilic myeloproliferative syndrome
    • Mitter, N.S. & Weiskopf, R.W. (1987) Unusual chromosome 7 aberrations in a case of eosinophilic myeloproliferative syndrome. Cancer Genetics and Cytogenetics, 26, 209-212.
    • (1987) Cancer Genetics and Cytogenetics , vol.26 , pp. 209-212
    • Mitter, N.S.1    Weiskopf, R.W.2
  • 49
    • 0025093035 scopus 로고
    • Hypereosinophilic syndrome with evolution to myeloproliferative disorder: Temporal relationship to loss of Y chromosome and c-N-ras activation
    • Needleman, S.W., Mane, S.M., Gutheil, J.C., Kapil, V., Heyman, M.R. & Testa, J.R. (1990) Hypereosinophilic syndrome with evolution to myeloproliferative disorder: temporal relationship to loss of Y chromosome and c-N-ras activation. Hematological Pathology, 4, 149-155.
    • (1990) Hematological Pathology , vol.4 , pp. 149-155
    • Needleman, S.W.1    Mane, S.M.2    Gutheil, J.C.3    Kapil, V.4    Heyman, M.R.5    Testa, J.R.6
  • 50
    • 2942568925 scopus 로고    scopus 로고
    • Rapid and complete response to imatinib mesylate (STI-571) in a patient with idiopathic hypereosmophilia
    • Nolasco, I., Carvalho, S. & Parreira, A. (2002) Rapid and complete response to imatinib mesylate (STI-571) in a patient with idiopathic hypereosmophilia. Blood, 100, 346b.
    • (2002) Blood , vol.100
    • Nolasco, I.1    Carvalho, S.2    Parreira, A.3
  • 51
    • 0032402207 scopus 로고    scopus 로고
    • Chronic eosinophilic leukemia and hypereosinophilic syndromes. Proposal for classification, literature review, and report of a case with unique chromosomal abnormality
    • Oliver, J.W., Deol, I., Morgan, D.L. & Tonk, V.S. (1998) Chronic eosinophilic leukemia and hypereosinophilic syndromes. Proposal for classification, literature review, and report of a case with unique chromosomal abnormality. Cancer Genetics and Cytogenetics, 107, 111-117.
    • (1998) Cancer Genetics and Cytogenetics , vol.107 , pp. 111-117
    • Oliver, J.W.1    Deol, I.2    Morgan, D.L.3    Tonk, V.S.4
  • 54
    • 0023195165 scopus 로고
    • Two dimensional and Doppler eehocardiographic findings in hypereosinophilic syndrome
    • Presti, C., Ryan, T. & Armstrong, W.F. (1987) Two dimensional and Doppler eehocardiographic findings in hypereosinophilic syndrome. American Heart Journal, 114, 172-175.
    • (1987) American Heart Journal , vol.114 , pp. 172-175
    • Presti, C.1    Ryan, T.2    Armstrong, W.F.3
  • 55
    • 0028932040 scopus 로고
    • α-interferon and hypereosinophilic syndrome with trisomy 8: Karyotypic remission
    • Quiquandon, I., Claisse, J.F., Capiod, J.C., Delobel, J. & Prin, L. (1995) α-interferon and hypereosinophilic syndrome with trisomy 8: karyotypic remission. Blood. 85, 2284-2285.
    • (1995) Blood , vol.85 , pp. 2284-2285
    • Quiquandon, I.1    Claisse, J.F.2    Capiod, J.C.3    Delobel, J.4    Prin, L.5
  • 58
    • 0023242966 scopus 로고
    • A myelodysplastic syndrome with eosinophilia associated with a break in the short arm of chromosome 16
    • Ross, F.M., Hamilton, M., Cook, M.K. & Irving, J.B. (1987) A myelodysplastic syndrome with eosinophilia associated with a break in the short arm of chromosome 16. Leukemia, 1, 680-681.
    • (1987) Leukemia , vol.1 , pp. 680-681
    • Ross, F.M.1    Hamilton, M.2    Cook, M.K.3    Irving, J.B.4
  • 59
    • 0036210261 scopus 로고    scopus 로고
    • Sequential transformation of t(8;13) related disease: A case report
    • Roy, S., Szer, J., Campbell, L.J. & Juneja, S. (2002) Sequential transformation of t(8;13) related disease: a case report. Acta Haematologica, 107, 95-97.
    • (2002) Acta Haematologica , vol.107 , pp. 95-97
    • Roy, S.1    Szer, J.2    Campbell, L.J.3    Juneja, S.4
  • 61
    • 0035823530 scopus 로고    scopus 로고
    • Rapid and complete control of idiopathic hypereosinophilia with imatinib mesylate
    • Schaller, J.L. & Burkland, G.A. (2001) Rapid and complete control of idiopathic hypereosinophilia with imatinib mesylate. http://www.medscape.com/viewarticle/408170 (accessed 1 February 2003). Med Gen Med 2001, 3, 9.
    • (2001) Med Gen Med , vol.3 , pp. 9
    • Schaller, J.L.1    Burkland, G.A.2
  • 63
    • 0029859432 scopus 로고    scopus 로고
    • A myeloproliferative disorder with eosinophilia associated with a unique translocation (3:5)
    • Shanske, A.L., Kalman, A. & Grunwald, H. (1996) A myeloproliferative disorder with eosinophilia associated with a unique translocation (3:5). British Journal of Haematology, 95, 524-526.
    • (1996) British Journal of Haematology , vol.95 , pp. 524-526
    • Shanske, A.L.1    Kalman, A.2    Grunwald, H.3
  • 66
    • 0036202529 scopus 로고    scopus 로고
    • Myeloproliferative disorders with translocations of chromosome 5q31-35: Role of the platelet-derived growth factor receptor beta
    • Steer, E.J. & Cross, N.C.P. (2002) Myeloproliferative disorders with translocations of chromosome 5q31-35: role of the platelet-derived growth factor receptor beta. Acta Haematologica, 107, 113-122.
    • (2002) Acta Haematologica , vol.107 , pp. 113-122
    • Steer, E.J.1    Cross, N.C.P.2
  • 67
    • 0018910993 scopus 로고
    • Eosinophilic leukaemia in association with a double Philadelphia chromosome
    • Stockdill, G., Hartley, S.E. & Allan, N.C. (1980) Eosinophilic leukaemia in association with a double Philadelphia chromosome. Postgraduate Medical Journal, 56, 268-270.
    • (1980) Postgraduate Medical Journal , vol.56 , pp. 268-270
    • Stockdill, G.1    Hartley, S.E.2    Allan, N.C.3
  • 71
    • 0017626122 scopus 로고
    • 1-negative eosinophilic leukemia with trisomy 8: Case report and review of cytogenetic studies
    • 1-negative eosinophilic leukemia with trisomy 8: case report and review of cytogenetic studies. Scandinavian Journal of Haematology, 18, 413-420.
    • (1977) Scandinavian Journal of Haematology , vol.18 , pp. 413-420
    • Weinfeld, A.1    Westin, J.2    Swolin, B.3
  • 72
    • 0027258339 scopus 로고
    • A unique chromosomal abnormality in idiopathic hypereosinophilic syndrome presenting with cardiac involvement
    • Wolz, D.E., Granato, J.E., Giles, H.R., Marks, S.M. & Grill, H.P. (1993) A unique chromosomal abnormality in idiopathic hypereosinophilic syndrome presenting with cardiac involvement. American Heart Journal, 126, 246-248.
    • (1993) American Heart Journal , vol.126 , pp. 246-248
    • Wolz, D.E.1    Granato, J.E.2    Giles, H.R.3    Marks, S.M.4    Grill, H.P.5
  • 74
    • 0031806213 scopus 로고    scopus 로고
    • Clinical and cytogenetic remission induced by interferon-α in a patient with chronic eosinophilic leukemia associated with a unique t(3;9;5) translocation
    • Yamada, O., Kitahara, K., Imamura, K., Ozasa, H., Okada, M. & Mizoguchi, H. (1998) Clinical and cytogenetic remission induced by interferon-α in a patient with chronic eosinophilic leukemia associated with a unique t(3;9;5) translocation. American Journal of Hematology, 58, 137-141.
    • (1998) American Journal of Hematology , vol.58 , pp. 137-141
    • Yamada, O.1    Kitahara, K.2    Imamura, K.3    Ozasa, H.4    Okada, M.5    Mizoguchi, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.