• 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

Clinical features of thalassemia.

作者信息

Ohene-Frempong K, Schwartz E

出版信息

Pediatr Clin North Am. 1980 May;27(2):403-20. doi: 10.1016/s0031-3955(16)33858-5.

DOI:10.1016/s0031-3955(16)33858-5
PMID:6155656
Abstract

The thalassemia syndromes are an important group of diseases in childhood, frequently encountered in many ethnic groups worldwide. Heterozygotes are frequently misdiagnosed as having iron deficiency anemia, and the more severely affected homozygotes present major problems in management. Advances in prenatal diagnosis offer hope for prevention, while progress in transfusion therapy, accuracy of prediction of value of splenectomy, and chelation therapy offer improved quality and, perhaps, duration of life.

摘要

相似文献

1
Clinical features of thalassemia.
Pediatr Clin North Am. 1980 May;27(2):403-20. doi: 10.1016/s0031-3955(16)33858-5.
2
[The treatment of intermediate thalassemia].
Haematologica. 1989 Oct;74(5 Suppl):252-65.
3
Current management of homozygous beta thalassemia.
Indian Pediatr. 1991 Oct;28(10):1221-9.
4
[Beta-thalassemias].
Ann Med Interne (Paris). 1983;134(2):147-59.
5
Update on thalassemia.地中海贫血最新进展
Pediatr Rev. 1992 Feb;13(2):55-62. doi: 10.1542/pir.13-2-55.
6
The interaction of alpha-thalassemia and homozygous sickle-cell disease.α地中海贫血与纯合子镰状细胞病的相互作用。
N Engl J Med. 1982 Jun 17;306(24):1441-6. doi: 10.1056/NEJM198206173062402.
7
Hematologic changes and hemoglobin analysis beta thalassemia heterozygotes during the first year of life.一岁以内β地中海贫血杂合子的血液学变化及血红蛋白分析
Pediatr Res. 1982 Apr;16(4 Pt 1):286-9. doi: 10.1203/00006450-198204000-00008.
8
beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four families.中间型β地中海贫血纯合子,伴有正常血红蛋白A2β地中海贫血。对四个家族的研究。
Acta Haematol. 1982;67(1):57-61. doi: 10.1159/000207025.
9
[Changes in hemoglobin fractions of pregnant women with heterozygous beta-thalassemia and iron deficiency anemia].[杂合子β地中海贫血合并缺铁性贫血孕妇血红蛋白组分的变化]
Akush Ginekol (Mosk). 1983 Dec(12):41-3.
10
Thalassemia.地中海贫血
Hematology Am Soc Hematol Educ Program. 2004:14-34. doi: 10.1182/asheducation-2004.1.14.

引用本文的文献

1
Effect of iron overload on exercise capacity in thalassemic patients with heart failure.铁过载对心力衰竭地中海贫血患者运动能力的影响。
Int J Cardiovasc Imaging. 2009 Dec;25(8):777-83. doi: 10.1007/s10554-009-9491-9. Epub 2009 Aug 13.
2
Evaluation of myocardial iron overload using magnetic resonance imaging.使用磁共振成像评估心肌铁过载。
Blood Transfus. 2009 Jul;7(3):183-7. doi: 10.2450/2008.0063-08.
3
Raised IgE levels in beta-thalassaemia: correlation with splenectomy and hepatitis B virus infection.β地中海贫血患者IgE水平升高:与脾切除术和乙型肝炎病毒感染的相关性
Clin Exp Immunol. 1984 Oct;58(1):199-205.