Segmental motor nerve conduction study in 162 patients with motor neuron disease

Motor neuron disease complicated by frontotemporal dementia: a case report

运动神经元病合并额颞痴呆1例报告

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Clinical study of single-fiber electromyography in patients with motor neuron diseases

单纤维肌电图检测运动神经元病患者临床研究

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The limbs function scores, total score of revised Norris scale, onset age and course of disease had no obvious correlation with the scores of ESD in patients with motor neuron disease ( P> 0.05).

运动神经元病患者肢体功能评分、改良Norris量表总评分、发病年龄、病程与扩充性痴呆量表各项评分无明显相关性（P>0.05）。

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In addition, the revised Norris scale was applied to measure the bulbar function and limbs function. The range of rating ranged from 0 ( the maximum harm) to 99 ( healthy).

采用改良的Norris量表测定运动神经元病患者的延髓功能、肢体功能，评分范围：0分为最大损害，99分为健康。

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Amyotrophic lateral sclerosis ( ALS)) is one of the motor neural diseases, which selectively affects motor neurons in the anterior horn of spinal-cord, and the motor nuclei of brainstem and the pyramidal cells in the motor cortex of brain.

肌萎缩侧索硬化症（amyotrophic lateral sclerosis）属运动神经元病的一种，该病选择性损害脊髓前角运动神经细胞、脑干颅神经运动神经核细胞、以及大脑运动皮质锥体细胞。

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Objective To investigate the curative effect of autologous bone marrow nuclear cells transplantation treating motor neuron disease ( MND), and to study the mechanism of this therapy.

目的观察自体骨髓有核细胞蛛网膜下腔移植治疗运动神经元病（MND）的疗效，并探讨其机制。

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Motor neuron disease ( MND) is a kind of unexplained for violation of brainstem motor nerve, damage to the spinal cord anterior horn cells and pyramidal tract as the main features of chronic progressive disease variability.

运动神经元病（Motor Neuron Disease MND）是一种原因不明的以侵犯脑干运动神经、损害脊髓前角细胞和锥体束为主要特征的慢性进行性变异性疾病。

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Objective To evaluate the diagnostic value of single-fiber electromyography ( SFEMG) in motor neuron diseases ( MND).

目的探讨单纤维肌电图检测运动神经元病（MND）的临床意义。

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Methods The levels of NSE and GM1 antibody in sera and CSF of30 patients with MND were analyzed with enzyme-linked immunosorbent assays ( ELISA).

目的通过测定运动神经元病（MND）患者血清和脑脊液（CSF）中神经元特异性烯醇化酶（NSE）和GM1抗体，初步探讨其临床意义。

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Etiology and mechanisms of motor neuron disease ( MND), a nervous system degeneration disease;

运动神经元病（MND）是一组神经系统变性病，至今病因及发病机理尚不清楚。

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Conclusions MMN should be differentiated from motor neuron disease and chronic inflammatory demyelinating polyneuropathy.

结论MMN应与运动神经元病和慢性炎性脱髓鞘性多发性神经根神经病鉴别。

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The Significance of NSE and GM1 Antibody in Sera and CSF of Patients with Motor Neuron Disease

运动神经元病患者血清和脑脊液中NSE和GM1抗体测定及其临床意义

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The Contents of immunoglobulin oligoclonal antibody IgM in serum were measured in 20 patients with motor neuron disease and 20 normal subjects.

作者对运动神经元病患者及健康对照者各20例血清免疫球蛋白单克隆抗体IgM含量进行了测定。

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Objective To elucidate the features of segmental motor nerve conduction studies in a large sample of motor neuron disease ( MND).

目的探讨运动神经元病（Motor neuron disease，MND）常规节段运动神经传导和位移技术检测的特点。

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Motor neurone disease went on to debilitate his body – but not his mind.

运动神经元病逐渐使他身体虚弱，却未影响他的大脑。

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Measurement of serum IgM level and treatment with prednison in patients with motor neuron disease

运动神经元病患者血IgM测定及大剂量强的松治疗研究

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The sensitivity of T 2-WI was highter than that of T 1-WI in spin echo series.

在自旋回波序列中，T2WI对多发性硬化症的敏感性高于T1WI。

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Early and late HHV-6 gene transcripts in multiple sclerosis lesions and normal appearing white matter

多发性硬化症损害与外观正常白质早发与迟发HHV-6的基因转录

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IFN-τ can prevent the development of experimental allergic encephalomyelitis ( EAE), an animal model for multiple sclerosis ( MS) in humans.

实验性变应性脑脊髓炎（EAE）是多发性硬化症（MS）的动物模型。IFN-τ能够抑制实验性脑脊髓炎的发生、发展。

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IL-15 is elevated in serum and cerebrospinal fluid of patients with multiple sclerosis

多发性硬化症患者的血清和脑脊液IL-15升高

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