利鲁唑
肌萎缩侧索硬化
兴奋毒性
依达拉奉
医学
病理生理学
神经科学
谷氨酸受体
随机对照试验
神经保护
疾病
麻醉
内科学
心理学
受体
作者
Alberto Benussi,Antonella Alberici,Maria Sofia Cotelli,Valentina Dell’Era,Valentina Cantoni,Elisa Bonetta,Rosa Manenti,Massimiliano Filosto,Roberta Morini,Abhishek Datta,Chris Thomas,Alessandro Padovani,Barbara Borroni
标识
DOI:10.1016/j.brs.2019.06.011
摘要
Amyotrophic lateral sclerosis (ALS) is a progressive disease which affects both upper and lower motor neurons, with a fatal prognosis, for which no curative treatment is currently available. Glutamate-driven excitotoxicity is supposed to be involved in its pathophysiology, and drugs such as riluzole or edaravone have shown to reduce disease progression in ALS to a limited extent.
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