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重视肌萎缩侧索硬化患者的认知和行为损害 被引量:4

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摘要 肌萎缩侧索硬化(amyotrophic lateral sclerosis,ALS)又称运动神经元病(motor neuron disease,MND),临床主要表现为进行性加重的肌肉萎缩、无力及痉挛,多于3~5年后因吞咽和呼吸困难而死亡,是一种主要累及脊髓前角细胞、脑干运动神经核及锥体束,
作者 樊东升
出处 《中华神经科杂志》 CAS CSCD 北大核心 2010年第9期603-606,共4页 Chinese Journal of Neurology
基金 国家自然科学基金资助项目(30871359),北京市自然科学基金资助项目(7082099)
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