Individuals with cerebellar ataxia could display dysdiadochokinesia.
小脑性共济失调患者可出现轮替运动障碍。
The clinical signs are hypoglycemia, ketonemia, ketonuria, disperse, anorexia, ataxia, anaesthesia and final death.
临床主要表现为低血糖、酮血、酮尿、离群、厌食、运动失调、麻木、最后死亡。
These signs are followed by ataxia.
这些症状之后就是共济失调。
共济失调的四种类型。
Other possible symptoms are ataxia, vertigo, seizures, and dysphagia.
其他可能的症状还有共济失调、眩晕、癫痫发作和吞咽困难。
Knuckling at fetlocks, ataxia, tail deviation and tail may be flaccid.
扣打距毛，运动失调，尾偏斜和尾可能松垂。
The typical clinical manifestations were vertigo and cerebellar ataxia.
最主要的临床表现为眩晕、小脑性共济失调。
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。
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。
Hypotension may occur as a symptom of overdose with signs of apathy and ataxia.
低血压可能发生，作为与冷漠和共济失调症状过量的迹象。
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。
Symptoms such as weakness, ataxia, and dragging of the toes start in the rear legs.
症状包括虚弱，共济失调和始发于后肢脚趾的行动不便。
Their clinical symptom includes walking unstable, speech disorder, ataxia, dystonia.
行走不稳，言语不清，共济失调，肌张力改变。
Objective To summarize the common types and medical reasons for acute infant ataxia.
目的总结小儿急性共济失调的常见类型与病因。
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。
Objective to investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.
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 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。
Methods The clinical datas of 36 infant patients suffering from acute ataxia are analyzed retrospectively.
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。
On admission, he was oriented, but had severe dysarthria, left-sided central facial palsy and gait ataxia.
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。
Objective: to study the possible relationship between mitochondrial DNA point mutations and hereditary 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 (HA).
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 role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3).
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 gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (SCA7).
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。
There was no relationship of BAC with the degree of changes in autonomic nervous function, blood pressure and ataxia.
自主神经功能、血压及共济运动的变化程度与血液中的酒精浓度无显著相关性。
In the 129mv subtypes, psychiatric signs were often associated with parkinsonism, followed by ataxia and myoclonus, whereas aphasia was rare.
在129MV中，精神病表现经常伴随震颤麻痹，随后为运动失调和肌阵挛，而失语症罕见。
Conclusion The patients with pure motor hemiparesis and dizziness, ataxia, dysarthria have more possibility to suffer from pontine infarction.
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。
Patients often present in one of three clinical stages. The first stage consists of cerebellar signs (such as ataxia), apathy and motor restlessness.
临床分期分三期，第一期包含有小脑症状（如共济失调），情感冷漠和坐立不安。
The clinical signs are hypoglycemia, ketonemia, ketonuria, disperse, anorexia, ataxia, anaesthesia and final death. To lucubrate the Pregnancy Toxemia of sheep.
临床主要表现为低血糖、酮血、酮尿、离群、厌食、运动失调、麻木、最后死亡。
Acute alcohol poisoning mostly involves in central nervous system, toxicities including ataxia, slurred speech, loss of equilibrium, coma and respiratory failure.
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.
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。
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