Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder that is marked by fasciculation, spasticity and progressive weakness of muscles, and results in difficulty speaking, swallowing and breathing. ALS is fatal, usually leading to death within a few years from diagnosis, although...
Amyotrophic lateral sclerosisis a chronic progressive degeneration ofmotor neuronsand has a high mortality.Riluzoleandedaravoneare the only approved medications currently being used foramyotrophic lateral sclerosisin clinical settings. However, they can lead to serious complications, such asinjuriesto the liv...
解析 (1)D.细节理解题.根据Amyotrophic lateral sclerosis,more commonly known as ALS,affects the nerve cells in the brain and spinal cord (脊髓) that make the muscles of both the upper and lower body work.可知,ALS使人们失去对肌肉运动的控制.故选D.(2)B.细节理解题.根据Hawking,diagnosed with t...
Amyotrophic lateral sclerosis (ALS) is the most common adult-onset motor neuron disorder characterized by progressive degeneration of cortical, bulbar, and spinal motor neurons. When a patient presents with a progressive upper and/or lower motor syndrome, clinicians must pay particular attention to ...
amyotrophic lateral sclerosis (ALS) āˌmīətrōfˈik, sklĭrōˈsĭs [key] or motor neuron disease, sometimes called Lou Gehrig's disease, degenerative disease that affects motor neurons in the brain and spinal cord, preventing them from se
肌萎缩侧索硬化(ALS)也叫运动神经元病(MND),后一名称英国常用,法国又叫夏科(Charcot)病,而美国也称卢伽雷(Lou Gehrig)病。我国通常将肌萎缩侧索硬化和运动神经元病混用,大众也俗称渐冻症。它是上运动神经元和下运动神经元损伤之后,导致包括球部(所谓球部,就是指的是延髓支配的这部分肌肉)、四肢、躯干、胸部腹...
Prion-like propagation of pathogenic proteins has been suggested to underlie several neurodegenerative diseases. In this Perspectives article, Braak et al. posit that progressive lesions in amyotrophic lateral sclerosis (ALS) spread through cell-to-cell
Amyotrophic Lateral Sclerosis (ALS) ALS is a progressive neurodegenerative disease that robs people of the ability to move and leads them to lose their ability to speak — and eventually breathe. Our Approach For over a decade, Biogen has been committed to advancing ALS research to provide a ...
概述肌萎缩侧索硬化(amyotrophiclateralsclerosis,ALS)是一种病因未明、主要累及大脑皮质、脑干和脊髓运动神经元的神经系统变性疾病。其局限性分型包括进行性球麻痹(PBP),连枷臂、腿… 幸孕基因 渐冻人-肌萎缩侧索硬化症的病因研究进展 Doctor莫 重症肌无力|一文读懂重症肌无力,病因,临床表现,治疗及忠告 刘昌坤发表于...
“渐冻症“是“肌萎缩侧索硬化(amyotrophic lateral sclerosisALS)的俗称,罹患该症的患者也被称为“渐冻症状”,这是一种神经系统疾病。支配肌肉运动的神经元慢慢变性、死亡,肌肉随之一点点萎缩,患者逐渐出现并加重肌无力、肌萎缩、吞咽困难、喝水呛咳以及说话不清等症状,逐渐失去运动能力和生活自理能力,直至死亡。“渐...