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少突胶质细胞功能障碍与肌萎缩侧索硬化症 被引量:1

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摘要 肌萎缩侧索硬化症(amyotrophic lateral sclerosis,ALS)是一种神经系统变性疾病,以大脑皮质、脑干、脊髓前角运动神经元选择性丢失为特征,目前发病机制不清,尚无有效治疗手段。大量研究表明运动神经元变性是一种非神经细胞自主性过程,星形胶质细胞和小胶质细胞参与神经元的死亡。
出处 《脑与神经疾病杂志》 2016年第5期327-330,共4页 Journal of Brain and Nervous Diseases
基金 国家自然科学基金项目(30900460 81171210)
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