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首页> 外文期刊>Inside R & D >1. EXPERIMENTAL DRUG FOR AMOTROPHIC LATERAL SCLEROSIS TREATMENT
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1. EXPERIMENTAL DRUG FOR AMOTROPHIC LATERAL SCLEROSIS TREATMENT

机译:1.实验药物的肌萎缩侧索硬化症治疗

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Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease, is a neurodegenerative disease that is characterized by muscular atrophy, difficulty in speaking, breathing, and an overall loss in muscular control across the body. Although the causes of ALS are manifold and their contributions imprecise, there is a genetic component to the disease. There is a known hereditary cause to the disease, although the precise location of the gene responsible for the disease is unclear. Other factors such as trauma to the head, environmental factors such as radiations, chemical exposure, and so on, have been suggested, but their contributions to the disease have largely been unclear. ALS is a common neuromuscular disease, affecting one or two people in a population of a 100,000 worldwide, every year.
机译:肌萎缩性侧索硬化症(ALS),也称为运动神经元病(MND)或Lou Gehrig病,是一种神经退行性疾病,其特征是肌肉萎缩,说话,呼吸困难和全身肌肉控制能力全面丧失。尽管ALS的病因多种多样,但其贡献不明确,但该疾病有遗传因素。尽管尚不清楚引起该疾病的基因的确切位置,但已知有导致该疾病的遗传原因。已经提出了其他因素,例如头部创伤,环境因素(例如辐射,化学暴露等),但是在很大程度上还不清楚它们对疾病的影响。 ALS是一种常见的神经肌肉疾病,每年都会影响全球100,000人口中的一两个人。

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    《Inside R & D》 |2014年第16期|1-3|共3页
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