Does absolute excess of alpha chains compromise the benefit of splenectomy in patients with thalassemia intermedia?
作者信息
Graziadei Giovanna, Refaldi Chiara, Barcellini Wilma, Cesaretti Claudia, Cassinero Elena, Musallam Khaled M, Cappellini Maria Domenica
出版信息
Haematologica. 2012 Jan;97(1):151-3. doi: 10.3324/haematol.2011.046730. Epub 2011 Oct 11.
Abstract
摘要
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Does absolute excess of alpha chains compromise the benefit of splenectomy in patients with thalassemia intermedia?α链绝对过量是否会损害中间型地中海贫血患者脾切除术的益处？
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本文引用的文献
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Optimal management of β thalassaemia intermedia.β 中间型地中海贫血的最佳管理。
Br J Haematol. 2011 Mar;152(5):512-23. doi: 10.1111/j.1365-2141.2010.08486.x. Epub 2011 Jan 20.
2
Redefining thalassemia as a hypercoagulable state.重新定义地中海贫血为一种高凝状态。
Ann N Y Acad Sci. 2010 Aug;1202:231-6. doi: 10.1111/j.1749-6632.2010.05548.x.
3
Splenectomy and thrombosis: the case of thalassemia intermedia.脾切除术与血栓：中间型地中海贫血病例。
J Thromb Haemost. 2010 Oct;8(10):2152-8. doi: 10.1111/j.1538-7836.2010.03940.x.
4
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.中间型地中海贫血患者的α珠蛋白基因四连体与β地中海贫血杂合子的关联。
Haematologica. 2009 Oct;94(10):1445-8. doi: 10.3324/haematol.2009.005728.
5
Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.涉及α-珠蛋白基因簇的节段性重复正在导致β-地中海贫血杂合子患者出现中间型β-地中海贫血表型。
Blood Cells Mol Dis. 2008 May-Jun;40(3):312-6. doi: 10.1016/j.bcmd.2007.11.006. Epub 2008 Jan 14.
6
Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification.16p13.3和11p15.4区域的9种未知重排导致α和β地中海贫血，通过高分辨率多重连接依赖探针扩增进行表征。
J Med Genet. 2005 Dec;42(12):922-31. doi: 10.1136/jmg.2005.033597. Epub 2005 May 13.
7
Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia.中间型地中海贫血脾切除患者的静脉血栓栓塞和高凝状态
Br J Haematol. 2000 Nov;111(2):467-73. doi: 10.1046/j.1365-2141.2000.02376.x.
8
Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia.由三个α-珠蛋白基因与杂合β-地中海贫血相互作用引起的不同血液学表型。
Am J Hematol. 1997 Jun;55(2):83-8. doi: 10.1002/(sici)1096-8652(199706)55:2<83::aid-ajh6>3.0.co;2-z.
9
10
The triplicated alpha-gene locus and heterozygous beta thalassaemia: a case of thalassaemia intermedia.三倍体α基因座与杂合β地中海贫血：1例中间型地中海贫血病例
Br J Haematol. 1983 Dec;55(4):709-10. doi: 10.1111/j.1365-2141.1983.tb02854.x.
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