肌萎缩

Objective To explore the clinical value of MRI and MR diffusion tensor imaging in amyotrophic lateral sclerosis.

目的 探讨常规MRI检查和MR扩散张量成像新技术在肌萎缩侧索硬化症中的临床应用价值。

Human gene therapy trial directed at Duchenne muscular dystrophy was launched yesterday at Columbus Children's Hospital, the Muscular Dystrophy Association, Children's Hospital, and Asklepios Biopharmaceutical Inc.

3月29日—俄亥俄州哥伦布市，美国第一个针对裘馨型肌萎缩症基因治疗人体试验昨天在哥伦布儿童医院开使进行。

In patients with amyotrophic lateral sclerosis without severe bulbar dysfunction, NIV improves survival with maintenance of, and improvement in, quality of life.

解释 对于没有严重的球麻痹的肌萎缩侧索硬化患者，NIV可提高有一定生存质量的生存期。

In patients with amyotrophic lateral sclerosis without seere bulbar dysfunction, NI improes surial with maintenance of, and improement in, quality of life.

解释对于没有严重的球麻痹的肌萎缩侧索硬化患者，NI可提高有一定生存质量的生存期。

Low signal was also seen in the motor cortex on T2-weighted images in three of the eight normal volunteers and four of the 16 disease controls: one with a bulbospinal muscular atrophy, two with leukoencephalopathy and one with Binswanger's disease.

在8例正常人对照者中有3例、16例其他神经疾病患者中有4例（1例脊髓延髓性肌萎缩症患者、2例表现为下肢痉挛性轻瘫的不明原因的白质脑病患者、1例表现为痴呆和下肢痉挛性轻瘫的皮质下动脉硬化性脑病患者）在T2像上于运动皮质区也可见低信号。

Objective To investigate the mutation of Cx32 gene, clinical and electrophysiological features of Chinese patients with Charcot-Marie-Tooth disease.

目的 分析X连锁腓骨肌萎缩症患者Cx32基因的突变及其临床表现和电生理特点。

In the first section ,clinical features of ALS patients were characterized as follows:(1) Thirty seven cases of definite and probable ALS patients (according to El Escorial criteria) were enrolled.

本研究旨在探讨肌萎缩侧索硬化新的诊疗手段，即质子磁共振波谱（1H-MRS）在患者的临床应用价值和ALS患者的谷氨酸测定。

PARTICIPANTS: Totally 32 patients suffered from ALS were recruited at the General Hospital of Chinese People's Armed Police from September 2006 to June 2007 according to the EL Escorial Criteria, including 21 males and 11 females, averagely aged (51±10) years. None of them developed subarachnoid occlusion.

对象：2006-09/2007-06武装警察部队总医院收治的肌萎缩侧索硬化患者32例，均符合EL Escorial诊断标准，经影像学和Queckenstedt试验确定不存在蛛网膜下腔阻塞，男21例，女11例，平均年龄（51±10）岁，其中有8例曾于6个月前行1个疗程神经干细胞移植治疗。

Other proteins such as α-synuclein and TDP43 for Parkinson and Frontotemporal lobar dementia/amyotrophic lateral sclerosis are also under investigation.

另外我们也在研究帕金森氏症的-synuclein及额颞叶失忆/肌萎缩侧索硬化症中的TDP43蛋白。

Its research is focused on six disorders: Alzheimer's disease, Parkinson's Disease, amyotrophic lateral sclerosis, prion diseases, frontotemporal dementia, and Huntington's disease.

该中心的研究主要集中于六种神经失调疾病：老年痴呆症，帕金森氏症，肌萎缩性侧索硬化症，朊病毒类疾病，额颞叶失智症以及亨廷顿舞蹈症等。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。