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神经系统多系统萎缩二例临床及病理报告 被引量:1

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摘要 神经系统多系统萎缩是一组原因不明或与遗传有关的神经元退行性病变,临床表现及诊断分型较繁杂。例1男性,63岁,因进行性走路不稳6年,发热3个月入院。6年前无原因出现发作性头晕,偶感走路不稳。2年后加重,3年后病情恶化,走路摇摆,言语变慢,曾两次晕厥。病...
作者 杨佐濂 朱克
出处 《中华神经科杂志》 CAS CSCD 1999年第3期192-192,共1页 Chinese Journal of Neurology
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  • 3Murayama S, Arima K, NakazatoY, et al. Immunocytochemical and ultrastructural studies of neuronal and oligodendroglial cytoplasmic inclusions in multipe system atrophy 2. oliagdendroglial cytoplasmic inclusions. Acta Neuropathol ,1992,84:32-38.
  • 4Kobayashi K, Miyazu K, Katsukawa K,et al. Cytoskeletal protein abnormalities in patients with olivopontocerebellar atrophy--an immunocytochemical and Gallyas silver impregnation study.J Neuropathol Appl Neurobiol, 1992,18:237-249.
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  • 6Papp MI, Lantos PL. Accumulation of tubular structures in oligodendroglial and neuronal cells as the basic alteration in multiple system atrophy.J Neurol Sci,1992,107:172-182.
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