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多系统萎缩患者的认知功能障碍 被引量:2

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摘要 多系统萎缩(multiple system atrophy,MSA)是一种散发进行性神经系统多部位受累的变性疾病。临床主要表现为帕金森样症候、小脑性共济失调、锥体束征和自主神经系统障碍等。少突胶质细胞内包涵体是该病的特征性病理学标志物,主要成分是一种高度磷酸化的α-突触核蛋白[1]。
出处 《中华内科杂志》 CAS CSCD 北大核心 2013年第6期517-518,共2页 Chinese Journal of Internal Medicine
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参考文献14

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二级参考文献11

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共引文献12

同被引文献18

  • 1刘建军,熊葶.多系统萎缩并发喘鸣一例报告[J].中华神经科杂志,2005,38(10):647-647. 被引量:2
  • 2王胜军,迟兆富,吴伟,侯金文,陈雯.多系统萎缩的临床与MRI特征[J].临床神经病学杂志,2006,19(2):86-89. 被引量:15
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  • 6Pedroso JL,Rivero RL,Barsottini OG.“Hot cross bun”sign resembling multiple system atrophy in a patient with Machado-Joseph disease.Arq Neuropsiquiatr,2013,71:824.
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  • 9Multiple-System Atrophy Research Collaboration.Mutations in COQ2in familial and sporadic multiple-system atrophy.N Engl J Med,2013,369:233-244.
  • 10Wenning GK,Geser F,Krismer F,et al.The natural history of multiple system atrophy:aprospective European cohort study.Lancet Neurol,2013,12:264-274.

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