剖析再生障碍性贫血后继发性骨髓增生异常综合征的基因组特征和临床过程：一个里程碑。

IF 5.1 2区医学 Q1 HEMATOLOGY

British Journal of Haematology Pub Date : 2024-11-14 DOI:10.1111/bjh.19898

Carmelo Gurnari, Valeria Visconte

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引用次数: 0

摘要

剖析再生障碍性贫血后继发性骨髓增生异常综合征的基因组特征和临床过程是一个里程碑。Li及其同事的报告研究了再生障碍性贫血和阵发性夜间血红蛋白尿患者演变为骨髓增生异常综合征和急性髓性白血病的决定因素，并特别关注移植后的预后。相关评论Li等：再生障碍性贫血后继发性骨髓增生异常综合征异基因造血干细胞移植的临床和遗传特征及预后。Doi: 10.1111/bjh.19855.

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Dissecting the genomic traits and clinical course of secondary myelodysplastic syndrome following aplastic anaemia: A milestone.

Dissecting the genomic traits and clinical course of secondary myelodysplastic syndrome following aplastic anaemia is a milestone. The report by Li and colleagues investigates determinants of evolution to myelodysplastic syndrome and acute myeloid leukaemia in patients with aplastic anaemia and paroxysmal nocturnal haemoglobinuria with a specific focus on post-transplant outcomes. Commentary on: Li et al. Clinical and genetic profiles and outcomes of allogeneic haematopoietic stem cell transplantation in secondary myelodysplastic syndrome following aplastic anaemia. Br J Haematol 2024 (Online ahead of print). doi: 10.1111/bjh.19855.

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来源期刊

British Journal of Haematology 医学-血液学

CiteScore

8.60

自引率

4.60%

发文量

565

审稿时长

1 months

期刊介绍： The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.