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Results: 1-7 |
Results: 7
Treatment response and residual-disease monitoring in initial and relapsedTEL-AML1 positive childhood ALL
Authors: Seeger, K Viehmann, S Buchwald, D Harbott, J Schrappe, M Stary, J Henze, G Trka, J
Citation: K. Seeger et al., Treatment response and residual-disease monitoring in initial and relapsedTEL-AML1 positive childhood ALL, LEUKEMIA, 15(2), 2001, pp. 280-282
Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life
Authors: Stanulla, M Kasper, B Schrappe, M Viehmann, S Harbott, J Ludwig, WD Welte, K
Citation: M. Stanulla et al., Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life, LEUKEMIA, 14(2), 2000, pp. 337-338
Quality assurance in RT-PCR-based BCR/ABL diagnostics - results of an interlaboratory test and a standardization approach
Authors: Burmeister, T Maurer, J Aivado, M Elmaagacli, AH Grunebach, F Held, KR Hess, G Hochhaus, A Hoppner, W Lentes, KU Lubbert, M Schafer, KL Schafhausen, P Schmidt, CA Schuler, F Seeger, K Seelig, R Thiede, C Viehmann, S Weber, C Wilhelm, S Christmann, A Clement, JH Ebener, U Enczmann, J Leo, R Schleuning, M Schoch, R Thiel, E
Citation: T. Burmeister et al., Quality assurance in RT-PCR-based BCR/ABL diagnostics - results of an interlaboratory test and a standardization approach, LEUKEMIA, 14(10), 2000, pp. 1850-1856
The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q
Authors: Borkhardt, A Bojesen, S Haas, OA Fuchs, U Bartelheimer, D Loncarevic, IF Bohle, RM Harbott, J Repp, R Jaeger, U Viehmann, S Henn, T Korth, P Scharr, D Lampert, F
Citation: A. Borkhardt et al., The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q, P NAS US, 97(16), 2000, pp. 9168-9173
Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AMLI gene fusion
Authors: Loncarevic, IF Roitzheim, B Ritterbach, J Viehmann, S Borkhardt, A Lampert, F Harbott, L
Citation: If. Loncarevic et al., Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AMLI gene fusion, GENE CHROM, 24(3), 1999, pp. 272-277
Multiplex PCR - a rapid screening method for detection of gene rearrangements in childhood acute lymphoblastic leukemia
Authors: Viehmann, S Borkhardt, A Lampert, F Harbott, J
Citation: S. Viehmann et al., Multiplex PCR - a rapid screening method for detection of gene rearrangements in childhood acute lymphoblastic leukemia, ANN HEMATOL, 78(4), 1999, pp. 157-162
Prednisone response is the strongest predictor of treatment outcome in infant acute lymphoblastic leukemia
Authors: Dordelmann, M Reiter, A Borkhardt, A Ludwig, WD Gotz, N Viehmann, S Gadner, H Riehm, H Schrappe, M
Citation: M. Dordelmann et al., Prednisone response is the strongest predictor of treatment outcome in infant acute lymphoblastic leukemia, BLOOD, 94(4), 1999, pp. 1209-1217
Risultati: 1-7 |