萎缩

Clinically, patients present with symptoms ranging from minor distal muscle weakness to complete sensorimotor paralysis.

临床上，病人出现的症状可以从轻微的末梢肌肉萎缩到完全的瘫痪。

The Dalian Shide Plastic Industry, Ltd. status of market research, analysis, identify the problems and implement the program and measures to change this situation and ensure its future long-term development.

本论文是对大连实德塑胶工业有限公司市场营销战略的研究，作为民营企业的大连实德塑胶工业有限公司，在产品市场需求旺盛，竞争激烈程度偏低的情况下，取得了显著的市场成绩，但目前出现了市场萎缩的不利局面，为改变这一状况，需要对企业的营销战略进行调整。

In the year of 841, ChangPogo died suddenly, and then Chunghaejin wasabolished, the activities in the Shilla people lived in the Tang Dynasty society had atrophiedgreatly.

第六章分析了清海镇废止以后9世纪后期东亚贸易出现的新的变化。841年张保皋突然死亡，接着清海镇被废除，在唐新罗人社会的活动大大萎缩。

Effect of insufficiency of the spleen qi on precancerosis was observed on the animal models with insufficiency of the speen qi and CAG.

结果脾气虚能加重慢性萎缩性胃炎的程度，与正常对照组比较，CAG组与脾气虚型CAG组，胃体粘膜固有层厚度明显减少（P＜0.01）；胃体腺腺底相对厚度减少（P＜0.05）；胃体粘膜核分裂相频数显著增加（P＜0.01）。

There is still no effective cure for spinocerebellar degeneration. This again proven that human still lacks of knowledge in brain related matters.

上网找资料后得知后脑萎缩症至今依然没有药方，这再次证实人类对人脑的认识非常贫乏。

Spinocerebellar ataxia is a condition that affects brain functions, such as coordination, speech and balance.Mr. Yang Wengang, who's from Hualien in Taiwan, has the disease. Although he knows his condition is incurable, Yang remains positive, and works hard to give his life meaning. Here is his story.

脊椎小脑萎缩症影响脑部功能，如步伐不协调、语言及平衡功能等，台湾花莲的杨文港就是罹患这种疾病，既使罹患这种无药可医的病，他还是正面面对人生，因为他了解，唯有靠著努力，才能真正感受到自己存在的意义，以下是杨文港的故事。

Spinocerebellar ataxia is an autosomal dominant hereditary neuron disorder disease.

脊髓小脑萎缩症(Spinocerebellar ataxia， SCA)是一种体染色体显性的遗传性神经元退化性疾病。

Since the identification of the first gene responsible for spinocerebellar ataxia type 1 (SCA1) in 1993, an increasing number of genes and chromosomal loci have been characterized.

我们收集到一个来自中国湖南望城的常染色体显性遗传SCA家系，主要临床特点为晚发缓慢进展的小脑性共济失调，起病年龄在40-52岁，平均47.25±4.37岁，可伴有痉挛性斜颈，头部MRI表现为小脑萎缩，家系未观察到遗传早现现象。

The studies were of predictive genetic testing for Huntington's disease, hereditary breast and ovarian cancer, familial adenomatous polyposis and spinocerebellar ataxia.

这些文献进行的研究包括了，杭丁顿氏症、遗传性乳癌及卵巢癌、家族性大肠腺肿症、小脑脊髓萎缩症等疾病之预报性遗传检验。

Objective To study the normal range of CAG repeats of dentatorubropallidoluysian atrophy gene in Han population of South China mainland,and the frequency of DRPLA CAG trinucleotide repeat expansion in spinocerebellar ataxia of China mainland.

目的研究中国大陆南方正常人群齿状核红核苍白球路易体萎缩基因n正常变异范围，以及DRPLA基因n扩展突变在中国大陆脊髓小脑型共济失调患者中的分布。

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。