ataxia

Objective To observe the effect of buspirone on ataxia symptom after stroke .

目的观察丁螺环酮对改善脑卒中后共济失调症状的临床疗效。

These signs are followed by ataxia .

这些症状之后就是共济失调。

The clinical characteristics and nursing measures of children with acute cerebellar ataxia

小儿急性小脑炎的临床特点和护理

Molecular Genetic Diagnosis and Clinical Analysis of Characteristics of Spinocerebellar Ataxia Type 2

脊髓小脑性共济失调2型的分子遗传学诊断及临床分析

Effect of Acupuncture on Balance Function of Ataxia Children with Cerebral Palsy

针刺疗法改善共济失调型脑性瘫痪平衡功能的疗效观察

Methods : Rotating rod method was used for examining ataxia ability of mice .

方法采用转棒法观察对乙醇所致小鼠平衡失调的影响。

Acute Cerebellar Ataxia : Clinical Analysis of 18 Cases

急性小脑性共济失调症18例临床分析

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia

2例华裔共济失调毛细血管扩张症患者的ATM基因突变分析

Population based study of late onset cerebellar ataxia in south east Wales

威尔士东南部地区一项关于迟发型小脑共济失调的人群调查研究

Results Virus infection is the main cause resulted in acute ataxia in infant .

结果病毒感染是急性共济失调的主要病因。

Distribution of different genotypes of hereditary ataxia in south China Accumulation and distribution ;

国内南方人群遗传性共济失调不同基因亚型的分布状况（英文）积累与分配的关系；

Note that Mr. Brain MRI of hereditary ataxia disease : case report

遗传性共济失调的头部MR影像1例

One case of report of poisonous fungus poisoning with ataxia

共济失调为首发症状的毒蕈中毒1例

Progress in the research of ataxia telangiectasia as a radiation sensitive syndrome

辐射敏感综合症&AT病研究进展

Treatment of Cerebellar Ataxia Using Transplantation of Embryonic Cerebellum Suspensions : Experimental Research

胚胎小脑悬液移植治疗小脑共济失调的实验研究

Role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3

细胞凋亡在脊髓小脑性共济失调3型发病机制中的作用

Analysis of the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7

遗传性脊髓小脑性共济失调7型的基因突变及临床特征分析

Ataxia ( a disorder of the nervous system affecting coordination , balance and speech )

共济失调（一种影响协调、平衡和语言功能的神经系统紊乱）

One Case Report of Ataxia Caused by Frontal Lobe Injury of Brain in Forensic Medicine

大脑额叶损伤致共济失调法医学鉴定1例

26 cases of acute cerebellar ataxia ( 77.2 % ) .

26例表现为急性小脑性共济失调，占77.2%。

Objective : To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia .

前言：目的：探索线粒体DNA点突变与遗传性共济失调的关系。

Observation of the effects of Frenkel training in patients with cerebellar ataxia

Frenkel训练法改善小脑性共济失调患者的疗效观察

ATM gene mutations in Chinese patients with ataxia - telangiectasia

中国人共济失调毛细血管扩张症ATM基因突变研究

Clinical and electrophysiological examination of 3 cases with sensory ataxia form Guillain-Barre Syndrome

感觉性共济失调型格林-巴利综合征3例临床与电生理

ObjectiveTo investigate the efficacy of acupuncture in ataxia children with cerebral palsy .

目的探讨针刺疗法治疗共济失调型脑瘫的疗效。

New calcium channel mutations predict aberrant RNA splicing in episodic ataxia

新的钙通道突变预示发作性共济失调患者的RNA异常剪接

Molecular Diagnostic Methods for Wilson Disease , Huntington Disease and Spinocerebellar Ataxia

肝豆状核变性、亨廷顿病和遗传性共济失调的分子诊断方法研究

Hereditary spastic ataxia & a report of 9 cases of 4 generations in one family

遗传性痉挛性共济失调&附1家族4代9例报告

Rehabilitative evaluation and treatment for patient with cerebellar ataxia

小脑性共济失调患者的康复评定与治疗

Sural amplitude was negatively correlated with disease duration and ataxia score .

腓肠神经的幅度与疾病持续时间、共济失调评分呈负相关。