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ataxia相关的网络例句

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与 ataxia 相关的网络例句 [注:此内容来源于网络,仅供参考]

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。

Objective To study the frequency distribution of spinocerebellar ataxia type 17 in mainland China and the normal range of CAG/CAA repeats of TATA-binding protein gene in Han population in southern China.

目的 研究中国大陆脊髓小脑性共济失调(spinocerebellar ataxias,SCA)17型(SCA17)的分布频率,以及南方汉族健康人群TATA结合蛋白(TATA-binding protein,TBP)基因CAG/CAA重复次数正常变异范围。

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。

To investigate the gene mutation of clinical and neuroelectrophysiological characteristics in Machado-Joseph disease. The gene mutation was detected in 45 patients diagnosed as spinocerebellar ataxia and 30 "healthy relatives". Brain stem evoked potentials, visual evoked potentials and motor conduction velocity and sensory conduction velocity were performed on MJD.

为了解Machado-Joseph病基因突变及临床的神经电生理特点,对16个诊断为遗传性小脑性共济失调家系的45例病人及30例家系的&正常&人作MJD基因突变分析,检出MJD基因的病人行肢体运动及感觉神经传导速度、脑干诱发电位,视觉诱发电位的检查。

He suffers spinocerebellar ataxia, or "SCA", a degenerative genetic disease that attacks a person's muscles and their ability to control them.

杨文港跪坐在地上,用双手挖地施肥播种,他罹患脊髓小脑萎缩症,一种渐进性退化性遗传疾病,影响人体肌肉的功能,但杨文港不向命运低头,开创出整片农园。

Objective Machado-Joseph disease/Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant neurodegenerative disorder caused by an expansion of polyglutamine tract near the C-terminus of the MJD1 gene product, ataxin-3. The precise mechanism of the MJD/SCA3 pathogenesis remains unclear.

目的 马查多-约瑟夫病/脊髓小脑共济失调3型,是由 MJD1基因产物ataxin-3的C-末端的多聚谷氨酰胺发生重复扩展突变而引起的一种常染色体显性遗传的神经退行性疾病,目前它的发病机制还不清楚。

Hereditary spinocerebellar ataxia Trinucleotide repeat Gene diagnosis

遗传性脊髓小脑型共济失调;三核苷酸重复;基因诊断

Piglet edema were first discovered in Britain, is hemolytic E. coli intestinal toxemia, so capillaries or systemic damage to the small blood vessels, increasing permeability and fluid extravasation too much water, to the head, eyelids, Equality ear edema, acute ataxia and death as the main feature of acute infectious diseases, also known as gastrointestinal edema pigs or pig intestinal toxemia E. coli, a highly lethal disease.

仔猪水肿病最早发现于英国,是由溶血性大肠杆菌引起肠毒血症,而使全身毛细血管或小血管受到破坏,通透性增大,水液外渗过多,造成的以头部、眼睑、耳部等处水肿、共济失调和急性死亡为主要特征的急性传染病,又称猪胃肠水肿或猪大肠杆菌肠毒血症,有高度致死性疾病。

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