1. 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。
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2. 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。
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3. These signs are followed by ataxia.
这些症状之后就是共济失调。
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4. The 4 types of ataxia.
共济失调的四种类型。
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5. 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。
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6. 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。
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7. 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。
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8. 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。
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9. 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。
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10. 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。
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11. 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。
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12. 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。
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13. 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。
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14. 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。
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15. 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。
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16. 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。
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17. 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。
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18. 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。
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19. 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。
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20. 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。
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21. 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。
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22. 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。
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23. 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。
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24. 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。
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25. 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。
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26. 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。
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27. 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。
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28. 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。
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29. 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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30. Acute alcohol poisoning mostly involves in central nervous system, toxicities including ataxia, slurred speech, loss of equilibrium, coma and respiratory failure.
