Prognostic significance of FLT3-ITD in pediatric acute myeloid leukemia: a meta-analysis of cohort studies. - Wikidata - awgldk - TriplyDB

Prognostic significance of FLT3-ITD in pediatric acute myeloid leukemia: a meta-analysis of cohort studies.

Prognostic significance of FLT3-ITD in pediatric acute myeloid leukemia: a meta-analysis of cohort studies.

http://www.wikidata.org/entity/Q30248904

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FLT3-ITD with DNMT3A R882 double mutation is a poor prognostic factor in Chinese patients with acute myeloid leukemia after chemotherapy or allogeneic hematopoietic stem cell transplantation.

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P2860

Prognostic significance of FLT3-ITD in pediatric acute myeloid leukemia: a meta-analysis of cohort studies.

http://www.wikidata.org/entity/Q30248904

description

2016 nî lūn-bûn

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2016 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2016 թվականի հուլիսին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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Prognostic significance of FLT ...... ta-analysis of cohort studies.

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Prognostic significance of FLT ...... ta-analysis of cohort studies.

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Prognostic significance of FLT ...... ta-analysis of cohort studies.

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Molecular and Cellular Biochemistry

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Prognostic significance of FLT ...... ta-analysis of cohort studies.

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Baoxi Zhang

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Chaonan Li

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Futian Ma

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Hongming Guo

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Huan Du

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Na Liu

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Xiaoli Wu

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Xiaoqing Zhao

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Xuefeng Feng

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P2860

Trim and fill: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis

Meta-analysis in clinical trials

The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration

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Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.

Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia.

Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis.

Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease.

Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia

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121-128

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