• 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

[Isochromosome 17q as the sole alteration in 2 patients with a myelodysplastic syndrome and its relation to myeloperoxidase activity].

作者信息

Solé F, Pérez A, Woessner S, Olmedo E, Florensa L, Sans J

机构信息

Unidad de Hematología y Oncología, Hospital Central L'Aliança de Barcelona.

出版信息

Sangre (Barc). 1991 Aug;36(4):323-5.

PMID:1663663
Abstract

Two patients diagnosed of myelodysplastic syndrome with an isochromosome i (17q) as the only chromosomal alteration are presented. The MAC method (i.e., morphology, antibodies, chromosomes) was applied in the study of one of the patients, it being found that all the myeloperoxidase-positive cells carried the i (17q) anomaly. Such finding might suggest that those patients with i (17q) as the only chromosomal alteration could have specific clinical and cytological features.

摘要

相似文献

1
[Isochromosome 17q as the sole alteration in 2 patients with a myelodysplastic syndrome and its relation to myeloperoxidase activity].
Sangre (Barc). 1991 Aug;36(4):323-5.
2
[Isochromosome 17q as the only cytogenetic change in a patient with refractory anemia with excess of blasts].17号等臂染色体作为伴有过多原始细胞的难治性贫血患者唯一的细胞遗传学改变
Sangre (Barc). 1991 Dec;36(6):515-6.
3
Eosinophilia-preceded myelodysplastic syndrome associated with deletion of chromosome 20q and isochromosome 17q.伴有20号染色体长臂缺失和17号等臂染色体的嗜酸性粒细胞增多先于骨髓增生异常综合征
Int J Hematol. 1999 Jan;69(1):59-60.
4
Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity?
Leuk Res. 1993 Aug;17(8):717-20. doi: 10.1016/0145-2126(93)90080-5.
5
Percentages of bone marrow blasts and chromosomal changes in patients with refractory anemia help to determine prognoses.难治性贫血患者的骨髓原始细胞百分比和染色体变化有助于判断预后。
Int J Hematol. 1994 Oct;60(3):207-13.
6
Sequential observation of clinical and karyotypic evolution in a patient with myelodysplastic syndrome.
Chin Med J (Engl). 1989 Sep;102(9):689-94.
7
Presence of peripheral blasts in refractory anemia and refractory cytopenia with multilineage dysplasia predicts an unfavourable outcome.难治性贫血和伴有多系发育异常的难治性血细胞减少症中出现外周血原始细胞预示着不良预后。
Leuk Res. 2008 Jan;32(1):33-7. doi: 10.1016/j.leukres.2007.02.021. Epub 2007 Apr 6.
8
[Refractory anemia showing excess of blasts (BAEB) that transformed into acute myelogenous leukemia (AML-M2) with a t (?8;20) chromosomal abnormality].[难治性贫血伴原始细胞增多(BAEB)转化为急性髓系白血病(AML-M2),伴有t(?8;20)染色体异常]
Gan No Rinsho. 1988 Dec;34(15):2109-13.
9
A specific cutaneous lesion revealing myelodysplastic syndrome.
Eur J Dermatol. 1998 Oct-Nov;8(7):517-8.
10
[Myelodysplastic syndromes: current diagnosis and classification].[骨髓增生异常综合征:当前的诊断与分类]
Ter Arkh. 2001;73(4):62-6.