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S Schnittger

Showing results (111-120 of 131) with videos related to

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Critical Reviews in Oncology/Hematology|October 7, 2005
Towards a pathogenesis-oriented therapy of acute myeloid leukemiaW Hiddemann, K Spiekermann, C Buske, et al.
Leukemia|January 18, 2008
NPM1-mutated acute myeloid leukaemia occurring in JAK2-V617F+ primary myelofibrosis: de-novo origin?L Pasqualucci, S Li, G Meloni, et al.
Leukemia|July 4, 2008
Simultaneous occurrence of acute myeloid leukaemia with mutated nucleophosmin (NPM1) in the same familyG Cazzaniga, L Lo Nigro, I Cifola, et al.
Leukemia|April 16, 2011
Development of standardized approaches to reporting of minimal residual disease data using a reporting software package designed within the European LeukemiaNetM Østergaard, C G Nyvold, J V Jovanovic, et al.
Leukemia|January 9, 2015
Molecular profiling of myeloid progenitor cells in multi-mutated advanced systemic mastocytosis identifies KIT D816V as a distinct and late eventM Jawhar, J Schwaab, S Schnittger, et al.
Leukemia|September 29, 2012
ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcomeS Schnittger, C Eder, S Jeromin, et al.
Leukemia|October 15, 2015
Additional mutations in SRSF2, ASXL1 and/or RUNX1 identify a high-risk group of patients with KIT D816V(+) advanced systemic mastocytosisM Jawhar, J Schwaab, S Schnittger, et al.
Leukemia|September 11, 2009
High dose ara-C in the treatment of newly diagnosed acute promyelocytic leukemia: long-term results of the German AMLCGE Lengfelder, C Haferlach, S Saussele, et al.
Leukemia|November 14, 2013
Landscape of genetic lesions in 944 patients with myelodysplastic syndromesT Haferlach, Y Nagata, V Grossmann, et al.
Leukemia|March 23, 2007
Recurrent finding of the FIP1L1-PDGFRA fusion gene in eosinophilia-associated acute myeloid leukemia and lymphoblastic T-cell lymphomaG Metzgeroth, C Walz, J Score, et al.
Pageof 14

Showing results (111-120 of 131) with videos related to

Sort By:
Pageof 14
Critical Reviews in Oncology/Hematology|October 7, 2005
Towards a pathogenesis-oriented therapy of acute myeloid leukemiaW Hiddemann, K Spiekermann, C Buske, et al.
Leukemia|January 18, 2008
NPM1-mutated acute myeloid leukaemia occurring in JAK2-V617F+ primary myelofibrosis: de-novo origin?L Pasqualucci, S Li, G Meloni, et al.
Leukemia|July 4, 2008
Simultaneous occurrence of acute myeloid leukaemia with mutated nucleophosmin (NPM1) in the same familyG Cazzaniga, L Lo Nigro, I Cifola, et al.
Leukemia|April 16, 2011
Development of standardized approaches to reporting of minimal residual disease data using a reporting software package designed within the European LeukemiaNetM Østergaard, C G Nyvold, J V Jovanovic, et al.
Leukemia|January 9, 2015
Molecular profiling of myeloid progenitor cells in multi-mutated advanced systemic mastocytosis identifies KIT D816V as a distinct and late eventM Jawhar, J Schwaab, S Schnittger, et al.
Leukemia|September 29, 2012
ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcomeS Schnittger, C Eder, S Jeromin, et al.
Leukemia|October 15, 2015
Additional mutations in SRSF2, ASXL1 and/or RUNX1 identify a high-risk group of patients with KIT D816V(+) advanced systemic mastocytosisM Jawhar, J Schwaab, S Schnittger, et al.
Leukemia|September 11, 2009
High dose ara-C in the treatment of newly diagnosed acute promyelocytic leukemia: long-term results of the German AMLCGE Lengfelder, C Haferlach, S Saussele, et al.
Leukemia|November 14, 2013
Landscape of genetic lesions in 944 patients with myelodysplastic syndromesT Haferlach, Y Nagata, V Grossmann, et al.
Leukemia|March 23, 2007
Recurrent finding of the FIP1L1-PDGFRA fusion gene in eosinophilia-associated acute myeloid leukemia and lymphoblastic T-cell lymphomaG Metzgeroth, C Walz, J Score, et al.
Pageof 14