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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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参考文献41

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二级参考文献48

  • 1康德瑄,樊东升.胸锁乳突肌肌电图在鉴别肌萎缩侧索硬化与颈椎病性脊髓病的研究[J].中国神经精神疾病杂志,1994,20(1):5-7. 被引量:47
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共引文献17

同被引文献104

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