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镰状细胞病:当前认识与未来选择

Sickle Cell Disease: Current Understanding and Future Options.

作者信息

Varelas Christos, Gavriilaki Eleni

机构信息

Hematology Department-BMT Unit, G .Papanicolaou Hospital, 57010 Thessaloniki, Greece.

2nd Propedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, 54644 Thessaloniki, Greece.

出版信息

J Clin Med. 2023 Sep 13;12(18):5943. doi: 10.3390/jcm12185943.

Abstract

Sickle cell disease (SCD) is a prevalent inherited hemoglobin disorder encompassing a cluster of congenital hemolytic anemias, each distinguished by the prevalence of sickle hemoglobin (HbS) [...].

摘要

镰状细胞病(SCD)是一种常见的遗传性血红蛋白疾病,包括一系列先天性溶血性贫血,每种贫血都以镰状血红蛋白(HbS)的 prevalence[... ]为特征。 (注:原文中“prevalence”此处表述似乎有误,可能影响对整句准确理解,正常可能是“presence”之类的词,可根据实际情况调整)

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本文引用的文献

1
Mitochondria: Emerging Consequential in Sickle Cell Disease.
J Clin Med. 2023 Jan 18;12(3):765. doi: 10.3390/jcm12030765.
3
Rate of Dental Extractions in Patients with Sickle Cell Disease.
J Clin Med. 2022 Oct 19;11(20):6174. doi: 10.3390/jcm11206174.
6
Complement in Sickle Cell Disease: Are We Ready for Prime Time?
J Blood Med. 2021 Mar 23;12:177-187. doi: 10.2147/JBM.S287301. eCollection 2021.
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Complement in sickle cell disease and targeted therapy: I know one thing, that I know nothing.
Blood Rev. 2021 Jul;48:100805. doi: 10.1016/j.blre.2021.100805. Epub 2021 Jan 21.
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Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition.
Hemoglobin. 2018 Sep-Nov;42(5-6):339-341. doi: 10.1080/03630269.2018.1540353. Epub 2019 Jan 9.
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Successful Outcome of Chronic Intrahepatic Cholestasis in an Adult Patient with Sickle Cell/ β (+) Thalassemia.
Case Rep Hematol. 2014;2014:213631. doi: 10.1155/2014/213631. Epub 2014 Feb 9.

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