• 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

相似文献

1
Erythropoiesis is not equally suppressed in transfused males and females with β-thalassemia major: are there clinical implications?重度β地中海贫血输血男性和女性的红细胞生成抑制程度不同：这有临床意义吗？
Haematologica. 2015 Aug;100(8):e292-4. doi: 10.3324/haematol.2014.118216. Epub 2015 Apr 24.
2
Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with β-thalassemia major: a longitudinal study.输血抑制成年重型β地中海贫血患者的红细胞生成并增加其铁调素：一项纵向研究。
Blood. 2013 Jul 4;122(1):124-33. doi: 10.1182/blood-2012-12-471441. Epub 2013 May 8.
3
Hepcidin and β-thalassemia major.铁调素与重型β地中海贫血。
Blood. 2013 Jul 4;122(1):3-4. doi: 10.1182/blood-2013-05-502617.
4
The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major.重度地中海贫血患者中促红细胞生成活性和铁负荷对铁调素表达的影响。
Haematologica. 2006 Jun;91(6):809-12.
5
Alpha and beta thalassemia.α和β地中海贫血
Am Fam Physician. 2009 Aug 15;80(4):339-44.
6
Levels of growth differentiation factor-15 are high and correlate with clinical severity in transfusion-independent patients with β thalassemia intermedia.β 中间型地中海贫血非输血依赖患者的生长分化因子 15 水平较高，与临床严重程度相关。
Blood Cells Mol Dis. 2011 Dec 15;47(4):232-4. doi: 10.1016/j.bcmd.2011.07.005. Epub 2011 Aug 23.
7
[Beta-thalassemia: clinical manifestations].[β地中海贫血：临床表现]
Bull Soc Pathol Exot. 2001 May;94(2):92-4.
8
Thalassemia diagnosis in a blood donor from a unique trimorphic red blood cell population observed in the recipient.
Clin Chem Lab Med. 2014 Sep;52(9):e205-6. doi: 10.1515/cclm-2014-0248.
9
Diagnosis of beta-thalassaemia major in previously transfused patients.既往输血患者重型β地中海贫血的诊断
J Coll Physicians Surg Pak. 2003 Jan;13(1):19-21.
10
Hematopoietic peripheral circulating blood stem cells as an independent marker of good transfusion management in patients with β-thalassemia: results from a preliminary study.造血外周循环血干细胞作为β地中海贫血患者良好输血管理的独立标志物：一项初步研究的结果
Transfusion. 2016 Apr;56(4):827-30. doi: 10.1111/trf.13452. Epub 2016 Jan 22.

引用本文的文献

1
[Guideline for transfusion management in Chinese children with transfusion-dependent thalassemia (2025)].[2025年中国儿童输血依赖型地中海贫血输血管理指南]
Zhongguo Dang Dai Er Ke Za Zhi. 2025 May 15;27(5):505-514. doi: 10.7499/j.issn.1008-8830.2410119.
2
Combination of a TGF-β ligand trap (RAP-GRL) and TMPRSS6-ASO is superior for correcting β-thalassemia.TGF-β 配体陷阱（RAP-GRL）与 TMPRSS6-ASO 的联合应用优于 β-地中海贫血的矫正。
Am J Hematol. 2024 Jul;99(7):1300-1312. doi: 10.1002/ajh.27332. Epub 2024 Apr 25.
3
Healthcare resource utilization and direct costs of transfusion-dependent thalassemia patients in Dubai, United Arab Emirates: a retrospective cost-of-illness study.阿联酋迪拜依赖输血的地中海贫血症患者的医疗资源利用和直接成本：一项回顾性疾病成本研究。
BMC Health Serv Res. 2022 Mar 5;22(1):304. doi: 10.1186/s12913-022-07663-6.
4
Spinal cord compression secondary to extramedullary hematopoiesis: A rareness in a young adult with thalassemia major.继发于髓外造血的脊髓压迫症：一名重型地中海贫血年轻成人患者中的罕见病例。
Acta Biomed. 2017 Aug 23;88(2):237-242. doi: 10.23750/abm.v88i2.6221.
5
Guidelines on Beta-thalassemia major - regular blood transfusion therapy: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular: project guidelines: Associação Médica Brasileira - 2016.重型β地中海贫血定期输血治疗指南：巴西血液学、血液治疗与细胞治疗协会：项目指南：巴西医学协会 - 2016年。
Rev Bras Hematol Hemoter. 2016 Oct-Dec;38(4):341-345. doi: 10.1016/j.bjhh.2016.09.003. Epub 2016 Sep 22.

本文引用的文献

1
Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with β-thalassemia major: a longitudinal study.输血抑制成年重型β地中海贫血患者的红细胞生成并增加其铁调素：一项纵向研究。
Blood. 2013 Jul 4;122(1):124-33. doi: 10.1182/blood-2012-12-471441. Epub 2013 May 8.
2
Prediction of blood volume in normal human adults.正常成年人血容量的预测。
Surgery. 1962 Feb;51(2):224-32.
3
How I treat thalassemia.我如何治疗地中海贫血症。
Blood. 2011 Sep 29;118(13):3479-88. doi: 10.1182/blood-2010-08-300335. Epub 2011 Aug 2.
4
Regulation of erythropoietin production.促红细胞生成素的产生调节。
J Physiol. 2011 Mar 15;589(Pt 6):1251-8. doi: 10.1113/jphysiol.2010.195057. Epub 2010 Nov 15.
5
Spinal cord compression in beta-thalassemia: case report and review of the literature.β地中海贫血中的脊髓压迫症：病例报告及文献综述
Spinal Cord. 2004 Feb;42(2):117-23. doi: 10.1038/sj.sc.3101544.
6
Reticulocyte counting in thalassaemia.
Clin Lab Haematol. 1996 Dec;18 Suppl 1:17-28.
7
Serum erythropoietin levels in thalassemia intermedia.中间型地中海贫血患者的血清促红细胞生成素水平
Ann Hematol. 1993 Oct;67(4):183-6. doi: 10.1007/BF01695865.
8
Relationship between transfusion regimen and suppression of erythropoiesis in beta-thalassaemia major.重型β地中海贫血输血方案与红细胞生成抑制之间的关系
Br J Haematol. 1995 Mar;89(3):473-8. doi: 10.1111/j.1365-2141.1995.tb08351.x.
9
Spinal cord compression in thalassemia. Report of 12 cases and recommendations for treatment.
Arch Intern Med. 1981 Jul;141(8):1033-6. doi: 10.1001/archinte.141.8.1033.
10
Clinical applications of measurement of serum immunoreactive levels of erythropoietin.
Ann N Y Acad Sci. 1985;459:375-81. doi: 10.1111/j.1749-6632.1985.tb20847.x.

Erythropoiesis is not equally suppressed in transfused males and females with β-thalassemia major: are there clinical implications?

作者信息

Hapgood Greg, Walsh Timothy, Cukierman Ronit, Paul Eldho, Cheng Ken, Bowden Donald K

机构信息

Haematology Department, Monash Health, Monash University, Melbourne, Australia

Medical Therapy Unit (Thalassemia Service), Monash Health, Monash University, Melbourne, Australia.

出版信息

Haematologica. 2015 Aug;100(8):e292-4. doi: 10.3324/haematol.2014.118216. Epub 2015 Apr 24.

DOI:10.3324/haematol.2014.118216
PMID:25911552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5004427/
Abstract
摘要