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Impact of Empagliflozin on the Outcomes of β-Thalassemia Major in Patients With Type 2 Diabetes Mellitus: The THALEMPA Observational Study.恩格列净对2型糖尿病重型β地中海贫血患者结局的影响:THALEMPA观察性研究
Cureus. 2024 Sep 21;16(9):e69837. doi: 10.7759/cureus.69837. eCollection 2024 Sep.
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Red blood cell alloimmunization in blood transfusion-dependent β thalassemia major patients in Sana'a City-Yemen.在也门萨那市依赖输血的β 地中海贫血症患者中,红细胞同种免疫。
Sci Rep. 2024 Jan 10;14(1):1005. doi: 10.1038/s41598-024-51561-2.
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The relationship of myocardial and liver T2* values with cardiac function and laboratory findings in transfusion-dependent thalassemia major patients: A retrospective cardiac MRI study.输血依赖型重型地中海贫血患者中心肌和肝脏T2*值与心功能及实验室检查结果的关系:一项心脏MRI回顾性研究
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Effects of Ramadan Intermittent Fasting on the Severity of β-Thalassemia Major Patients.斋月间歇性禁食对重型β地中海贫血患者严重程度的影响。
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The Effect of Long-Term Iron Chelator Therapy on Serum Levels of Hepcidin and Ferritin in Patients with Thalassemia Major and Intermediate.长期铁螯合剂治疗对重型和中间型地中海贫血患者血清铁调素和铁蛋白水平的影响。
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Long-Term Effects of Iron Chelating Agents on Ocular Function in Patients with Thalassemia Major.铁螯合剂对重型地中海贫血患者眼功能的长期影响。
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本文引用的文献

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
β-thalassemias: paradigmatic diseases for scientific discoveries and development of innovative therapies.β地中海贫血:科学发现与创新疗法开发的典型疾病。
Haematologica. 2015 Apr;100(4):418-30. doi: 10.3324/haematol.2014.114827.
3
Understanding GRADE: an introduction.了解 GRADE:简介。
J Evid Based Med. 2013 Feb;6(1):50-54. doi: 10.1111/jebm.12018.
4
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.
5
Red cell alloimmunization in a diverse population of transfused patients with thalassaemia.红细胞同种免疫在输血地中海贫血患者的多样化人群中。
Br J Haematol. 2011 Apr;153(1):121-8. doi: 10.1111/j.1365-2141.2011.08576.x. Epub 2011 Feb 17.
6
Beta-thalassemia.β-地中海贫血。
Orphanet J Rare Dis. 2010 May 21;5:11. doi: 10.1186/1750-1172-5-11.
7
Amelioration of Sardinian beta0 thalassemia by genetic modifiers.遗传修饰因子对撒丁岛β0地中海贫血的改善作用。
Blood. 2009 Oct 29;114(18):3935-7. doi: 10.1182/blood-2009-04-217901. Epub 2009 Aug 20.
8
Alpha and beta thalassemia.α和β地中海贫血
Am Fam Physician. 2009 Aug 15;80(4):339-44.
9
Effect of transfusional iron intake on response to chelation therapy in beta-thalassemia major.输血性铁摄入对重型β地中海贫血螯合治疗反应的影响。
Blood. 2008 Jan 15;111(2):583-7. doi: 10.1182/blood-2007-08-109306. Epub 2007 Oct 19.
10
[Evidence based clinical practice. Part 1--well structured clinical questions].循证临床实践。第1部分——结构完善的临床问题
Rev Assoc Med Bras (1992). 2003 Oct-Dec;49(4):445-9. doi: 10.1590/s0104-42302003000400039. Epub 2004 Feb 4.

Guidelines on Beta-thalassemia major - regular blood transfusion therapy: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular: project guidelines: Associação Médica Brasileira - 2016.

作者信息

Langhi Dante, Ubiali Eugênia Maria Amorim, Marques José Francisco Comenalli, Verissimo Mônica de Almeida, Loggetto Sandra Regina, Silvinato Antonio, Bernardo Wanderley Marques

机构信息

Faculdade de Ciências Médicas da Santa Casa de São Paulo (FCMSCSP), São Paulo, SP, Brazil.

Hemocentro de Ribeirão Preto, Ribeirão Preto, SP, Brazil.

出版信息

Rev Bras Hematol Hemoter. 2016 Oct-Dec;38(4):341-345. doi: 10.1016/j.bjhh.2016.09.003. Epub 2016 Sep 22.

DOI:10.1016/j.bjhh.2016.09.003
PMID:27863763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5119672/
Abstract
摘要