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肌萎缩侧索硬化运动神经元选择性损伤的可能发病机制 被引量:4

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摘要 肌萎缩侧索硬化(ALS)是一组病因未明确致命性的选择性侵犯脊髓前角细胞、脑干运动神经核、皮质锥体细胞和锥体束的进展性的神经退行性疾病,既有上运动神经元受损,又有下运动神经元受损,表现为肌无力、肌萎缩、延髓麻痹与锥体束征。
出处 《中国老年学杂志》 CAS CSCD 北大核心 2013年第4期972-975,共4页 Chinese Journal of Gerontology
基金 国家自然科学基金资助项目(No.30560042 81160161)
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