cerebellar ataxia

The typical clinical manifestations were vertigo, cerebellar ataxia as well as nystagmus.

临床表现以眩晕、呕吐 、 小脑性共济失调、眼球震颤为主.

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The Molecular Mechanism of Hereditary Cerebellar Ataxia in Waddles Mouse

Waddles小鼠遗传性小脑性共济失调的分子机制的研究

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based on their nursing 15 children with acute cerebellar ataxia, the authors summed up the clinical characteristics of acute cerebellar ataxia including: ( 1) multi-pathogenesis;

通过对15例急性小脑炎患儿护理，认为其临床特点有：（1）多病因；

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On the basis of animal experiment, 9~ 12 week human embryonic cerebellar tissue suspension was transplanted into the cerebellum of 6 medically intractable patients with severe hereditary cerebellar degenerative ataxia.

在动物实验基础上，将胎龄为9～12周的人胚胎小脑组织悬液移植到6例患有严重小脑萎缩的患者脑内。

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aim: to study the dyssynergia cerebellaris myoclonica ( ramsay hunt) with myoclonus, epilepsia and cerebellar ataxia as major symptoms according to the analysis of cases and the review of literatures, in order to improve the cognition of clinicians on ramsay hunt.

目的：通过病例分析及文献资料复习对肌阵挛、癫痫及小脑性共济失调为核心症状的肌阵挛性小脑协调不能（即Ramsay Hunt综合征）进行探讨，以提高临床医师对其的认识。

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Progressive cerebellar ataxia was the main clinical symptom, other manifestations included extrapyramidal system and pyramidal tract sign and orthostatic hypotension. MRI showed atrophy olf cerebellum and brainstem.

临床表现为进行性小脑性共济失调，可伴有锥体外系症状，锥体束征及直立性低血压。

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Non-progressive congenital ataxia with cerebellar hypoplasia in three families

对患小脑发育不全相关的先天性非进行性共济失调的3个家族患儿的研究

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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%。

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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

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Study on heredo-cerebellar-atrophy-ataxia in calf

犊牛遗传性小脑萎缩共济失调研究报告

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