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- gamma motor neuron γ运动神经元 γ运动神经原,γ运动神经元
- gamma motor neuron r 抑制性神经元
- Each of the 100 microwires lay beside a single motor neuron. 那100根金属丝每一根都靠近单一个运动神经元；
- gamma motor neurone r 抑制性神经元
- Weakened muscle with less than normal tone. A lower motor neuron symptom . 一种较低的运动神经元症状，肌肉比正常的还要衰弱。
- A typical result of an upper motor neuron lesion is paralysis of voluntary movement. 典型的上位运动神经之损伤就会导致随意运动麻痹。
- A neurologic examination may detect disorientation, an abnormal gait, altered reflexes, and sensory or motor neuron abnormalities. 神经系统检查可发现定位异常、步态异常、反射改变及感觉或运动神经元异常。
- The patient was a 71 year old man who developed muscle wasting and weakness and had electromyographic evidence of motor neuron disease. 患者是71岁男性,渐发肌肉萎缩和无力,肌电图描记的证据显示为运动神经元病。
- ALS is a rapidly progressive, fatal disease characterized by loss of muscular control resulting from motor neuron degeneration and death. ALS是一个进展迅速的不治之症，临床表现为肌肉控制力的丧失，病因是运动神经元的变性和死亡。
- Gliosis around motor neurons was seen. 神经元周围胶质细胞增生。
- The 14 cases fulfilled probable or definite ALS E1 Escorial categories having upper and lower motor neuron signs. 依据Escorial诊断标准,14例连枷臂综合征患者均符合确诊或拟诊的肌萎缩侧索硬化。
- Objective To study survival motor neuron (SMN) deletion in adult-onset patients with spinal muscular atrophy (SMA). 目的探讨成年起病的脊肌萎缩症(SMA)患者的运动神经元存活基因SMN的缺失情况。
- Polyneuropathy usually involves motor nerve dysfunction, also known as lower motor neuron disease. 神经丛神经病通常伴有运动神经功能障碍，也称为下位运动神经元病。
- Phillips has one candidate cell in mind: the motor neuron, which directs muscles from the brain and spinal cord. 菲力普斯心目中有个理想目标，就是运动神经元，它也是脑与脊髓控制肌肉的媒介。
- The axon of a somatic motor neuron leaves the CNS and travels without interruption to the innervated effector cell. 轴突的体运动神经元离开中枢神经系统和旅行而不中断向神经细胞的效应。
- Objective This study examined the prevalence of deletion and subtle mutations of survival motor neuron( SMN) gene in children with spinal muscular atrophy( SMA). 目的研究儿童型脊肌萎缩症(MA)者中运动神经元生存基因缺失与微突变情况。
- Objective To investigate the relationship between survival motor neuron(SMN)gene and the clinical features of childhood spinal muscular atrophy(SMA). 目的探讨运动神经元存活基因与儿童期脊肌萎缩症临床特征的关系。
- Clinical for muscular dystrophy, myasthenia gravis, muscular dystrophy, polymyositis, motor neuron disease, such as atrophy disease syringomyelia. 临床用于肌肉萎缩、重症肌无力、肌营养不良、肌炎、运动神经元病、脊髓空洞症等痿症。
- A single motor neuron may innervate more than one fiber. A motor neuron plus all of the muscle fibers that it innervates comprise a motor unit. 运动单位是由一个运动神经元及其所支配的一定数量的肌纤维所构成。
- Rather, they only synapse on VM lower motor neurons ipsilaterally. 腹正中下神经元控制著轴向运动。
