1.Methods 60 normal subjects and 22 patients with motor neurone disease(MND) were detected.
方法检测正常人60例,MND患者22例。
2.Effects of Lead on Neurone Cells and Distribution of Calcium in Rat Brian
铅对大鼠脑神经细胞钙分布和侧棘数的影响
3.They will usually have diseases considered incurable, such as advanced cancer or motor neurone disease.
他们所患疾病必须是不治之症，如晚期癌症或运动神经疾病。
4.Conclusions Paraneoplastic Syndrome with colon cancer and matastatic lung cancer may manifest as motor neurone-like syndrome.
结论肠癌合并副肿瘤综合征可表现为运动神经元病。
5.Disordered sensori-motor control, resulting from an upper motor neurone lesion, presenting as intermittent or sustained involuntary activation of muscles.
“由于上运动神经元损伤导致的感觉－运动控制障碍，表现为肌肉的间断性或持续性的不自主运动”。
6.Objective To investigate the clinic, electrophysiological, pathological characters of paraneoplastic syndrome which manifested with motor neurone disease-like.
摘要目的探讨以运动神经元病为表现的副肿瘤综合征的临床、电生理学、病理学特点。
7.He is the first of four patients with spinal cord(6) injuries, muscular dystrophy(7), stroke or motor neurone(8) disease testing the brain-to-movement system developed in Massachusetts.
四个分别患有脊髓损伤，肌肉失调，中风和运动神经元疾病的病人参与测试了这个在马萨诸塞州研制成功的大脑支配行动的装置。雷是他们中的第一个。
8.②In the model and NGF treatment group, nestin positive cells mostly coexisted with glial fibrillary acidic protein on the 3rd day, and double stained with neurone specific enolase was obviously increased on the 14th day.
②模型组和神经生长因子治疗组3d时缺血皮质巢蛋白阳性突起主要与胶质纤维酸性蛋白共存,14d时巢蛋白与神经元特异性烯醇化酶共存明显增多。
9.Immunocytochemistry was used to identify cell types. Results:MSC cultured in medium containing DMEM/ 10% FBS/ neural growth factors proliferated quickly. The neuron-like cells appeared at 7-9 d with the expression of neurone specific enolase(NSE) at(52±9.2)% and glial fibrillary acidic protein(GFAP) at(15±7)%,and could survive more than 7 days;
结果:在DMEM/10%胎牛血清培养液中加入神经生长因子后MSC增殖速度加快,培养7~9 d后有神经元样细胞形成,表达神经元特异性烯醇化酶(NSE)为(52±9.2)%,神经胶质原纤维酸性蛋白(GFAP)为(15±7)%,细胞分化后继续培养仍可存活7 d以上。
