Congenital B-lymphoblastic leukemia with a cryptic MLL rearrangement and post-treatment evolution to mixed phenotype acute leukemia

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Congenital B-lymphoblastic leukemia with a cryptic MLL rearrangement and post-treatment evolution to mixed phenotype acute leukemia

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Congenital B-lymphoblastic leu ...... mixed phenotype acute leukemia

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type

Item

label

Congenital B-lymphoblastic leu ...... mixed phenotype acute leukemia

@en

prefLabel

Congenital B-lymphoblastic leu ...... mixed phenotype acute leukemia

@en

P1476

Congenital B-lymphoblastic leu ...... mixed phenotype acute leukemia

@en

P2093

Cecilia Fu

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Elizabeth Moschiano

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Gordana Raca

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Paul K Pattengale

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P2860

Acquisition of a CD19-negative myeloid phenotype allows immune escape of MLL-rearranged B-ALL from CD19 CAR-T-cell therapy

The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias

The MLL recombinome of acute leukemias in 2013.

Lineage switching in acute leukemias: a consequence of stem cell plasticity?

Biology and treatment of infant leukemias.

Identification of Mixed Lineage Leukemia Gene (MLL)/MLLT10 Fusion Transcripts by Reverse Transcription-PCR and Sequencing in a Case of AML With a FISH-Negative Cryptic MLL Rearrangement.

Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients.

Outcome of congenital acute lymphoblastic leukemia treated on the Interfant-99 protocol.

Congenital MLL-positive B-cell acute lymphoblastic leukemia (B-ALL) switched lineage at relapse to acute myelocytic leukemia (AML) with persistent t(4;11) and t(1;6) translocations and JH gene rearrangement

P304

29-32

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P31

scholarly article

case report

P356

10.1016/J.LRR.2016.07.002

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P478

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P50

Matthew J. Oberley

P577

2016-08-02T00:00:00Z

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P698

27547725

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P921

birth defect

P932

4982915

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