Case 2 and case 3 also developed upper motor neurons impairment at the lower limbs and cognitive impairment. 例2和例3还同时合并下肢上运动神经元损害及认知功能障碍。
Through the prolong of central motor conducting time, motor evoked potential reveals the clinical and subclinical changes of upper motor neurons, especially the subclinical damages of multiple sclerosis and exerts an accessory role in the diagnosis. 通过中枢运动传导时间延长,揭示临床及亚临床的上运动神经元改变,尤其适用于发现中枢性运动神经元病变的多发性硬化亚临床改变,起到支持辅助诊断作用。
A Study of Transcranial Magnetic Stimulation Motor Evoked Potentials on Amyotrophic Lateral SclerosisBackground: Amyotrophic lateral sclerosis ( ALS) is a progressive neurodegenerative disease affecting both lower and upper motor neurons ( UMN). 肌萎缩侧索硬化症(amyotrophiclateralsclerosis,ALS)是一种慢性进行性神经系统变性病,以上、下运动神经元变性为特征。
Amyotrophic lateral sclerosis ( ALS) is a progressive neurodegenerative disease, selectively involving the upper and lower motor neurons that control voluntary movement. 肌萎缩侧索硬化(amyotrophiclateralsclerosis,ALS)是一种支配随意运动的上下运动神经元选择性受累的神经系统变性疾病。
20 patients with severe intoxication had the symptom of upper motor neurons paralysis in about 1 month after invasion. 3~7d后,出现由下肢远端开始的多发性周围神经病表现;重度中毒患者(20例)于发病1个月左右开始出现上运动元麻痹的表现。
Objective To observe the expression of phosphorylated neurofilaments of the upper and lower motor neurons in experimental autoimmune gray matter disease ( EAGMD) animal model. 目的观察实验性自身免疫性灰质病模型中上、下运动神经元磷酸化神经丝表达的特征。