Clinical features of childhood acute myeloid leukaemia with specific gene rearrangements

Author:

Frascella E,Rondelli R,Pigazzi M,Zampieron C,Fagioli F,Favre C,Lippi A A,Locatelli F,Luciani M,Menna G,Micalizzi C,Rizzari C,Testi A M,Pession A,Basso G

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Reference8 articles.

1. Forestier E, Heim S, Blennow E, Borgstrom G, Holmgren G, Heinonen K et al. Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001. Br J Haematol 2003; 121: 566–577.

2. Biondi A, Rovelli A, Cantù-Rajnoldi A, Fenu S, Basso G, Luciano A et al. Acute promyelocytic leukaemia in children: experience of the Italian Pediatric Hematology and Oncology Group (AIEOP). Leukemia 1994; 8: 1264–1268.

3. Martinez-Climent JA, Lane NJ, Rubin CM, Morgan E, Johnstone HS, Mick R et al. Clinical and prognostic significance of chromosomal abnormalities in childhood acute myeloid leukemia de novo. Leukemia 1995; 9: 95–101.

4. Grimwade D, Walker H, Oliver F, Wheatley K, Harrison C, Harrison G et al. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1612 patients entered into MRC 10 trial. Blood 1998; 92: 2322–2333.

5. Raimondi SC, Chang MN, Ravindranath Y, Behm FG, Gresik MV, Steuber CP et al. Chromosomal abnormalities in 478 children with acute myeloid leukemia: clinical characteristics and treatment outcome in a cooperative Pediatric Oncology Group Study – POG8821. Blood 1999; 94: 3707–3716.

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