结果病毒感染是急性共济失调的主要病因。
Results Virus infection is the main cause resulted in acute ataxia in infant.
共济失调的四种类型。
目的总结小儿急性共济失调的常见类型与病因。
Objective To summarize the common types and medical reasons for acute infant ataxia.
目的：探索线粒体dna点突变与遗传性共济失调的关系。
Objective: to study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia.
回顾小脑性共济失调的研究历史、分类，介绍脊髓小脑共济失调的病因机制和治疗方法。
The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed. The pathogenesis and treatments of spinocerebellar ataxia were summarizd.
目的总结小儿急性共济失调的常见类型与病因方法对36例急性共济失调患儿的临床资料进行回顾性分析。
Objective To summarize the common types and medical reasons for acute infant ataxia. Methods The clinical datas of36infant patients suffering from acute ataxia are analyzed retrospectively.
目的研究遗传性脊髓小脑性共济失调7型（SCA7）的基因突变和临床特征。
Objective To study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (SCA7).
目的研究细胞凋亡在脊髓小脑性共济失调3型(SCA3)分子发病机制中的作用。
Objective to study the role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3).
低血压可能发生，作为与冷漠和共济失调症状过量的迹象。
Hypotension may occur as a symptom of overdose with signs of apathy and ataxia.
症状包括虚弱，共济失调和始发于后肢脚趾的行动不便。
Symptoms such as weakness, ataxia, and dragging of the toes start in the rear legs.
目的研究线粒体dna点突变与遗传性共济失调(HA)的关系。
Objective to study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia (HA).
目的分析泛素依赖的蛋白水解通路(UPP)在转染了脊髓小脑性共济失调3型(SCA3)基因的PC 12细胞中的定位及作用。
Objective To analyze the role and location of ubiquitin-dependent proteolysis pathway (UPP) in PC12 cells transfected by plasmids with spinocerebellar ataxia type 3 (SCA3) gene.
方法对36例急性共济失调患儿的临床资料进行回顾性分析。
Methods The clinical datas of 36 infant patients suffering from acute ataxia are analyzed retrospectively.
结论通过这次研究，发现SCA1、SCA2、SCA3型在不明原因的共济失调中的发生率为22.8%，其中又以SCA3型为主，确定诊断的最直接最有效的手段是基因诊断。
Conclusion the incidence of SCA1, SCA2 and SCA3 is 22.8% in patients with ataxia of unknown origin, and SCA3 is main type. Genetic analysis is the most effective means for the diagnosis of SCA.
结论纯运动性偏瘫患者，如果出现构音障碍、头晕及共济失调时应考虑到桥脑梗死的可能。
Conclusion The patients with pure motor hemiparesis and dizziness, ataxia, dysarthria have more possibility to suffer from pontine infarction.
目的探讨针刺疗法治疗共济失调型脑瘫的疗效。
ObjectiveTo investigate the efficacy of acupuncture in ataxia children with cerebral palsy.
腓肠神经的幅度与疾病持续时间、共济失调评分呈负相关。
Sural amplitude was negatively correlated with disease duration and ataxia score.
急性酒精中毒对中枢神经系统的影响，症状有共济失调、语言含糊、平衡失调、昏迷及呼吸系统衰竭。
Acute alcohol poisoning mostly involves in central nervous system, toxicities including ataxia, slurred speech, loss of equilibrium, coma and respiratory failure.
MS的症状包括视力模糊、平衡缺失、共济失调、极度疲劳、瘫痪和失明。目前尚无可以治愈的方法。
Ms symptoms may include blurred vision, loss of balance, poor coordination, extreme fatigue, paralysis and blindness. There is no cure.
方法选取有共济失调症状的脑卒中患者30例口服丁螺环酮治疗，治疗前后分别用共济失调量表进行评定，与未服丁螺环酮的对照组30例进行比较。
Methods 30 patients with ataxia after stroke were treated with buspirone, other 30 patients without buspirone as controls. Before and after treatment, they were assessed with ataxia-scale.
最主要的临床表现为眩晕、小脑性共济失调。
The typical clinical manifestations were vertigo and cerebellar ataxia.
目的探讨共济失调毛细血管扩张症的细胞遗传学异常特点。
Objective to investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.
其他可能的症状还有共济失调、眩晕、癫痫发作和吞咽困难。
Other possible symptoms are ataxia, vertigo, seizures, and dysphagia.
入院时，患者定向力正常，但表现出严重的构音障碍，左侧中枢性面瘫，共济失调步态。
On admission, he was oriented, but had severe dysarthria, left-sided central facial palsy and gait ataxia.
更详细的临床检查还发现共济失调和诊断成像，包括前，后的对比计算机断层扫描，发现一个老骨折C2 。
More detailed clinical examination also revealed ataxia, and diagnostic imaging, including pre- and post-contrast computed tomography, revealed an old fracture of C2.
AT M基因突变可导致共济失调毛细血管扩张症(AT)，一种常染色体隐性遗传病，该病特点是不协调的肌肉运动和神经退化。
Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.
结果：本组病人以恶心呕吐、眩晕和共济失调为常见临床表现，而头痛和颈项强直仅分别见于5 1.6 %和32 .3%的病人。
Results:Symptoms such as nausea, vomiting, dizziness and dystaxia were common in this group of patients, and headache and nuchal rigidity were found in 51.6% and 32.3% patients respectively.
目的探讨感觉性共济失调型CIDP的临床特点和发病机理。
Objective To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS.
目的探讨感觉性共济失调型CIDP的临床特点和发病机理。
Objective To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS.
应用推荐