Pediatric acute myeloid leukemia as classified using 2008 WHO criteria: a single-center experience.
暂无分享,去创建一个
K. Davis | A. Cherry | D. Arber | N. Marina | G. Dahl | Lisa Ma | Amy Heerema-McKenney | Amy E Heerema-McKenney
[1] G. Armstrong,et al. Long-term risk for subsequent leukemia after treatment for childhood cancer: a report from the Childhood Cancer Survivor Study. , 2011, Blood.
[2] E. van den Berg,et al. Cytogenetics of childhood acute myeloid leukemia: United Kingdom Medical Research Council Treatment trials AML 10 and 12. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[3] R. Hills,et al. Prognostic significance of CEBPA mutations in a large cohort of younger adult patients with acute myeloid leukemia: impact of double CEBPA mutations and the interaction with FLT3 and NPM1 mutations. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[4] Y. Hayashi,et al. Prognostic significance of the BAALC isoform pattern and CEBPA mutations in pediatric acute myeloid leukemia with normal karyotype: a study by the Japanese Childhood AML Cooperative Study Group , 2010, International journal of hematology.
[5] Susan C. Weber,et al. STRIDE - An Integrated Standards-Based Translational Research Informatics Platform , 2009, AMIA.
[6] D. Arber,et al. A comparison of two methods for screening CEBPA mutations in patients with acute myeloid leukemia. , 2009, The Journal of molecular diagnostics : JMD.
[7] R. Larson. Therapy-related myeloid neoplasms , 2009, Haematologica.
[8] S. Raimondi,et al. Prevalence and prognostic implications of CEBPA mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group. , 2009, Blood.
[9] J. Merker,et al. Clinical characterization of acute myeloid leukemia with myelodysplasia-related changes as defined by the 2008 WHO classification system. , 2008, Blood.
[10] S. Pileri,et al. NPM1 mutations and cytoplasmic nucleophosmin are mutually exclusive of recurrent genetic abnormalities: a comparative analysis of 2562 patients with acute myeloid leukemia , 2008, Haematologica.
[11] S. Adachi,et al. Acute Myeloid Leukemia with Multilineage Dysplasia in Children , 2007, International journal of hematology.
[12] R. Arceci,et al. The incidence and clinical significance of nucleophosmin mutations in childhood AML. , 2007, Blood.
[13] S. Raimondi,et al. Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study. , 2007, Blood.
[14] C. Bloomfield,et al. A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare ‘poor prognosis’ myeloid malignancies , 2006, Leukemia.
[15] Gerhard Ehninger,et al. Prevalence and prognostic impact of NPM1 mutations in 1485 adult patients with acute myeloid leukemia (AML). , 2006, Blood.
[16] Stefan Fröhling,et al. Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations. , 2005, Blood.
[17] D. Webb. Optimizing therapy for myeloid disorders of Down syndrome , 2005, British journal of haematology.
[18] C. Preudhomme,et al. CEBPA point mutations in hematological malignancies , 2005, Leukemia.
[19] Paola Fazi,et al. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. , 2005, The New England journal of medicine.
[20] D. Liang,et al. CEBPα mutations in childhood acute myeloid leukemia , 2004, Leukemia.
[21] J. Radich,et al. FLT3 internal tandem duplication in 234 children with acute myeloid leukemia: prognostic significance and relation to cellular drug resistance. , 2003, Blood.
[22] M. Slovak,et al. Prognostic Impact of Acute Myeloid Leukemia Classification , 2003 .
[23] M. Slovak,et al. Prognostic impact of acute myeloid leukemia classification. Importance of detection of recurring cytogenetic abnormalities and multilineage dysplasia on survival. , 2003, American journal of clinical pathology.
[24] M. Tomonaga,et al. Cytogenetic heterogeneity of acute myeloid leukaemia (AML) with trilineage dysplasia: Japan Adult Leukaemia Study Group‐AML 92 study , 2003, British journal of haematology.
[25] T. Rebbeck,et al. Differential bone marrow aspirate DNA yields from commercial extraction kits , 2002, Leukemia.
[26] J. Bennett,et al. Evaluation of the dysmyelopoiesis in 336 patients with de novo acute myeloid leukemia: major importance of dysgranulopoiesis for remission and survival. , 1992, Leukemia.
[27] F. Naeim. 21 – Acute Myeloid Leukemia, Not Otherwise Specified , 2013 .
[28] R. Pieters,et al. Favorable prognostic impact of NPM1 gene mutations in childhood acute myeloid leukemia, with emphasis on cytogenetically normal AML , 2009, Leukemia.
[29] J. Bennett,et al. B-Lymphoblastic Leukemia/Lymphoma , 2014 .