神经萎缩的

Amyotrophic lateral sclerosis is a fatal neurodegenerative disease that is familial in 10% of cases.

肌萎缩性侧束硬化症是一种致命的神经退化性疾病，其家族遗传率是10%。

OBJECTIVE: To investigate the humoral immune response pattern for amyotrophic lateral sclerosis patients after neural stem cell transplantation.

目的：研究肌萎缩侧索硬化患者神经干细胞移植后中枢内的体液免疫反应模式。

Olfactory ensheathing cell transplantation can improve nerve function in amyotrophic lateral sclerosis patients, and delay progressive aggravation of patients' condition.

嗅鞘细胞移植近期能改善肌萎缩侧索硬化患者的神经功能，延缓病情的进行性恶化。

This study was to evaluate the influence of masseter muscle on the craniofacial growth and development by using the botulinum neurotoxin to cause the masseter muscle atrophy.

中文摘要本研究目的是藉由将肉毒杆菌神经毒素注射入大白鼠咬肌，使咬肌萎缩，来探讨咬肌对颅颜型态及生长发育的影响。

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。

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。

Neuroimaging: Medial Temporal Lobe Atrophy Rating Scale (0-4) and Age-Related White Matter Changes Scale (0-30), assessing white matter hyperintensities; and lacune counts.

神经影像学方面：评估白质高信号和陷窝计数使用了内侧颞叶萎缩等级量表（0－4分）、年龄相关的白质改变量表（0－30分）。

These results show that the damage to visual function is earlier than the change in the thickness of the retinal neurepithelium in the macular region in 40 early non-exudative eyes.

这说明，年龄相关性萎缩型黄斑变性患者视功能改变早于视网膜神经上皮层的厚度改变，对于早期患者可优先选择电生理检查。

Thus, he was admitted on June 23, 2002 for comprehensive rehabilitation. Physical examination revealed muscle power in the upper limbs, as grade 4, bilateral hand grasp as grade 3, lower limbs as grade 4, and atrophy of the intrinsic muscles of both hands. Deep tendon reflex was absent in the bilateral legs.

入院后身体检查发现上肢肌力为4分，但两手握力为3分，手部小肌肉明显萎缩，下肢肌力为4分，深部肌腱反射上肢皆为1+，下肢皆敲不出，四肢末端感觉都缺损，为典型的多发性神经病变。

We report a 19 year-old female patient presenting with juvenile-onset diabetes mellitus, bilateral optic atrophy, high frequency hearing impairment, and gaze evoked nystagmus, but without diabetes insipidus, urinary tract abnormality or other obvious signs of neurodegeneration.

本文报告一位十九岁女孩并有幼年型胰岛素依赖型糖尿病，视神经萎缩，听觉障碍及眼震颤；但并未有尿崩症，尿道异常及其他明显的退化性神经病变。

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。