• 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

[地中海贫血中红细胞生成的细胞学特征。I. 骨髓中红细胞生成有核成分的功能特征]

[Cytological characteristics of erythropoiesis in thalassemia. I. Functional characteristics of the nucleated elements of erythropoiesis in the bone marrow].

作者信息

Kosinetz G I, Buikova I A, Mamedowa T A

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(2):240-7.

PMID:6159264
Abstract

In 24 patients affected with thalassaemia of various degrees of seriousness the functional condition of nuclear cells or red serie was investigated in the bone-marrow. The investigation was carried out by analyzing partial erythroblastogrammes, evaluating proliferative activity according to the 3H-thymidine marking index and determining ineffective erythropoiesis by means of nucleated PAS-positive erythroblasts. The findings reveal the degree of seriousness of the disease being directly dependent on the extent of functional disturbances in the cells of the erythropoietic system.

摘要

对24例不同严重程度的地中海贫血患者的骨髓有核细胞或红细胞系的功能状况进行了研究。通过分析部分幼红细胞象、根据3H-胸腺嘧啶核苷标记指数评估增殖活性以及借助有核PAS阳性幼红细胞确定无效红细胞生成来进行该项研究。研究结果显示,疾病的严重程度直接取决于红细胞生成系统细胞功能紊乱的程度。

相似文献

1
[Cytological characteristics of erythropoiesis in thalassemia. I. Functional characteristics of the nucleated elements of erythropoiesis in the bone marrow].[地中海贫血中红细胞生成的细胞学特征。I. 骨髓中红细胞生成有核成分的功能特征]
Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(2):240-7.
2
[Cytological characteristics of erythropoiesis in thalassemia. II. Structural functional characteristics of peripheral blood erythrocytes].[地中海贫血中红细胞生成的细胞学特征。II. 外周血红细胞的结构功能特征]
Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(2):248-55.
3
[Erythroblastic proliferative kinetics in homozygous beta-thalassemic children in relation to transfusional treatment].[纯合子β地中海贫血患儿红细胞增殖动力学与输血治疗的关系]
Minerva Pediatr. 1977 Jan 14;29(1):45-54.
4
[The erythropoietic reaction and its bone marrow retention in thalassemia major].[重型地中海贫血的红细胞生成反应及其骨髓潴留情况]
Nouv Rev Fr Hematol Blood Cells. 1977;18(1):220-1.
5
Globin chain precipitation, deranged iron metabolism and dyserythropoiesis in some thalassaemia syndromes.
Haematologia (Budap). 1984;17(1):35-55.
6
[Cytological criteria for assessing the severity of the erythropoietic disorders in thalassemia].[地中海贫血中评估红细胞生成障碍严重程度的细胞学标准]
Probl Gematol Pereliv Krovi. 1979 Nov;24(11):16-9.
7
[In-vitro studies on the kinetics of bone-marrow erythropoesis during the first trimester of life (Trimenonreduction)].[关于生命头三个月骨髓红细胞生成动力学的体外研究(孕期头三个月减少)]
Padiatr Padol. 1975;10(4):347-81.
8
Ineffective erythropoiesis in haemoglobin E beta -thalassaemia: an electron microscope study.血红蛋白Eβ地中海贫血中无效红细胞生成的电子显微镜研究。
Br J Haematol. 1981 Jul;48(3):451-7. doi: 10.1111/j.1365-2141.1981.tb02737.x.
9
[Microcytological characteristics of reticulocytes in heterozygous beta-thalassemia].
Boll Soc Ital Biol Sper. 1983 Oct 30;59(10):1569-75.
10
Relation between erythropoiesis and bone metabolism in thalassemia.
N Engl J Med. 1981 Jun 11;304(24):1470-3. doi: 10.1056/NEJM198106113042406.