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注意:仅列出部分参考文献,下载原文获取全部文献信息。Genomic and Gene Expression Profiling Defines Indolent Forms of Mantle Cell Lymphoma
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Time to Treatment Does Not Influence Overall Survival in Newly Diagnosed Mantle-Cell Lymphoma
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JOURNAL OF CLINICAL ONCOLOGY (2009)
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Hypermutation in mantle cell lymphoma does not indicate a clinical or biological subentity
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A new prognostic index (MIPI) for patients with advanced-stage mantle cell lymphoma
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Histopathology, cell proliferation indices and clinical outcome in 304 patients with mantle cell lymphoma (MCL):: a clinicopathological study from the European MCL Network
M Tiemann et al.
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IgVH mutations in blastoid mantle cell lymphoma characterize a subgroup with a tendency to more favourable clinical outcome
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Immunoglobulin heavy chain genes somatic hypermutations and chromosome 11q22-23 deletion in classic mantle cell lymphoma: a study of the Swiss Group for Clinical Cancer Research
F Bertoni et al.
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The leukemic presentation of mantle-cell lymphoma: Disease features and prognostic factors in 58 patients
E Matutes et al.
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VH mutation status and VDJ rearrangement structure in mantle cell lymphoma:: correlation with genomic aberrations, clinical characteristics, and outcome
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A subset of t(11;14) lymphoma with mantle cell features displays mutated IgVH genes and includes patients with good prognosis, nonnodal disease
J Orchard et al.
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Molecular heterogeneity in MCL defined by the use of specific VH genes and the frequency of somatic mutations
FI Camacho et al.
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Frequency of gastrointestinal involvement and its clinical significance in mantle cell lymphoma
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The proliferation gene expression signature is a quantitative integrator of oncogenic events that predicts survival in mantle cell lymphoma
A Rosenwald et al.
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Splenectomy in mantle cell lymphoma with leukaemia: a comparison with chronic lymphocytic leukaemia
R Ruchlemer et al.
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The splenic form of mantle cell lymphoma
MK Angelopoulou et al.
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Efficacy of splenectomy for patients with mantle cell non-Hodgkin's lymphoma
Y Yoong et al.
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Mantle cell lymphoma, in leukaemic phase with prominent splenomegaly. A report of eight cases with similar clinical presentation and aggressive outcome
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