• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

A review of 125 cases to determine the risk of myelodysplasia and leukemia in pediatric neutropenic patients after treatment with recombinant human granulocyte colony-stimulating factor.

作者信息

Imashuku S, Hibi S, Nakajima F, Mitsui T, Yokoyama S, Kojima S, Matsuyama T, Nakahata T, Ueda K, Tsukimoto I

出版信息

Blood. 1994 Oct 1;84(7):2380-1.

PMID:7522628
Abstract
摘要

相似文献

1
A review of 125 cases to determine the risk of myelodysplasia and leukemia in pediatric neutropenic patients after treatment with recombinant human granulocyte colony-stimulating factor.一项对125例病例的回顾性研究，以确定重组人粒细胞集落刺激因子治疗后儿童中性粒细胞减少症患者发生骨髓增生异常综合征和白血病的风险。
Blood. 1994 Oct 1;84(7):2380-1.
2
Monosomy 7 and activating RAS mutations accompany malignant transformation in patients with congenital neutropenia.7号染色体单体和激活型RAS突变伴随先天性中性粒细胞减少症患者的恶性转化。
Blood. 1995 Dec 15;86(12):4579-86.
3
Acute monocytic leukemia in a patient with severe congenital neutropenia after treatment with recombinant human granulocyte colony-stimulating factor.一名严重先天性中性粒细胞减少症患者在接受重组人粒细胞集落刺激因子治疗后发生急性单核细胞白血病。
J Pediatr Hematol Oncol. 1996 Nov;18(4):422-4. doi: 10.1097/00043426-199611000-00023.
4
Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy.接受粒细胞集落刺激因子（G-CSF）治疗的先天性中性粒细胞减少症患者的骨髓增生异常综合征和急性髓系白血病
Blood. 2000 Jul 15;96(2):429-36.
5
Can treatment with recombinant granulocyte colony-stimulating factor transform neutropenia into leukemia?重组粒细胞集落刺激因子治疗会将中性粒细胞减少症转化为白血病吗？
J Pediatr. 1995 Nov;127(5):845-6. doi: 10.1016/s0022-3476(95)70195-8.
6
Granulocyte colony-stimulating factor and congenital neutropenia--risk of leukemia?粒细胞集落刺激因子与先天性中性粒细胞减少症——白血病风险？
J Pediatr. 1996 Jul;129(1):187-8. doi: 10.1016/s0022-3476(96)70238-x.
7
Transformation of congenital neutropenia into monosomy 7 and acute nonlymphoblastic leukemia in a child treated with granulocyte colony-stimulating factor.一名接受粒细胞集落刺激因子治疗的儿童先天性中性粒细胞减少症转化为单体7及急性非淋巴细胞白血病。
J Pediatr. 1995 Feb;126(2):263-5. doi: 10.1016/s0022-3476(95)70557-0.
8
Kostmann's disease, recombinant HuG-CSF, monosomy 7 and MDS/AML.科茨曼病、重组人粒细胞集落刺激因子、单体7以及骨髓增生异常综合征/急性髓系白血病
Br J Haematol. 1995 Sep;91(1):150-3. doi: 10.1111/j.1365-2141.1995.tb05260.x.
9
Myelodysplastic syndrome and acute myelogenous leukemia as a late clonal complication in children with acquired aplastic anemia.骨髓增生异常综合征和急性髓性白血病作为获得性再生障碍性贫血患儿的晚期克隆性并发症。
Blood. 1997 Aug 1;90(3):1009-13.
10
Detection of myelodysplastic syndrome/ acute myeloid leukemia evolving from aplastic anemia in children, treated with recombinant human G-CSF.检测接受重组人粒细胞集落刺激因子治疗的儿童再生障碍性贫血演变而来的骨髓增生异常综合征/急性髓系白血病。
Haematologica. 2003 Nov;88(11):ECR31.

引用本文的文献

1
Long-term outcome of a randomized controlled study in patients with newly diagnosed severe aplastic anemia treated with antithymocyte globulin and cyclosporine, with or without granulocyte colony-stimulating factor: a Severe Aplastic Anemia Working Party Trial from the European Group of Blood and Marrow Transplantation.一项针对新诊断的重型再生障碍性贫血患者进行的随机对照研究的长期结果，这些患者接受了抗胸腺细胞球蛋白和环孢素治疗，联合或不联合粒细胞集落刺激因子：来自欧洲血液和骨髓移植组的重型再生障碍性贫血工作组试验。
Haematologica. 2020 May;105(5):1223-1231. doi: 10.3324/haematol.2019.222562. Epub 2019 Oct 3.
2
Establishment of a monosomy 7 leukemia cell line, MONO-7, with a ras gene mutation.
Int J Hematol. 2002 Jan;75(1):72-7.
3
Prolonged bone marrow failure with monosomy 7 after engraftment failure following bone marrow transplantation.骨髓移植后植入失败后出现伴有7号染色体单体的长期骨髓衰竭。
Int J Hematol. 2001 Feb;73(2):258-61. doi: 10.1007/BF02981947.
4
Clinical toxicity of cytokines used as haemopoietic growth factors.用作造血生长因子的细胞因子的临床毒性。
Drug Saf. 1995 Dec;13(6):371-406. doi: 10.2165/00002018-199513060-00006.