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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。

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。

3·These signs are followed by ataxia.

这些症状之后就是共济失调。

4·The 4 types of ataxia.

共济失调的四种类型。

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。

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。

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。

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。

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。

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。

共济失调

1·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。

2·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。

3·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。

4·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。

5·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。

运动失调

1·In the 129mv subtypes, psychiatric signs were often associated with parkinsonism, followed by ataxia and myoclonus, whereas aphasia was rare.

在129 MV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。

2·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。