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ataxic lymphopathy [医] 共济失调性淋巴[组织]病
These signs are followed by ataxia. 这些症状之后就是共济失调。
It results in progressive ataxia beginning at a young age. 该疾病自幼犬期发病并导致渐进性共济失调。
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。
Conclusion Scalp and neck acupuncture has an exact effect on apoplectic ataxia. 结果头项针治疗中风共济失调总有效率100%25,明显优于对照组(76%25)。
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。
Babinski signs were negative.Gait was slow, broadbased, and tandem walking was ataxic. 步态沉重，缓慢，似鸭步，属共济失调。
The function of moral self subduing or making factors orderly meals that moral self can turn ataxic factors into a system. 要素统合功能是指，道德自我能将各种零碎的、无序的、模糊的、相互对立的道德要素统合成一个组织化的、清晰的、有层次的体系；
The patient was a 51 year old woman with a history of rapidly progressive cognitive impairment and ataxia of gait. 患者系51岁女性，有呈急性进行性发展的认知损害和步态共济失调病史。
Neurologic symptoms of hypermagnesemia are muscular weakness, paralysis, ataxia, drowsiness, and confusion. 高镁血症的神经系统症状表现为肌肉无力、瘫痪、共济失调、嗜睡和意识模糊。
A neurologic syndrome occurred in the morning with unusual headache and stroke-like episodes, presenting an acute ataxic hemiparesis and a pure motor hemiparesis, respectively. 两病人临床表现皆始于清晨，因剧烈头痛及类似中风症状，一以失调性偏瘫，另一以纯运动性偏瘫运动性偏瘫而住院。
Of them, none had ataxia or other neurological sign, except strabismus or amblyopia in 3 and familial history in 2. 由临床徵候来看，先天性眼振患者均无步态不稳或其他神经学症状，少数则伴有斜视、弱视及家族史；
A story of a brave man who despite his spinocerebellar ataxia refuses to give up volunteering. 一个罹患小脑萎缩症患者、不因生病放弃做志工的故事。
Their clinical symptom includes walking unstable,speech disorder,ataxia,dystonia. 临床表现:行走不稳,言语不清,共济失调,肌张力改变。
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 gene mutation and clinical characteristics of hereditary spinocerebellar ataxia type 7 (SCA7). 摘要目的研究中国人遗传性脊髓小脑型共济失调(SCA)7型(SCA7)的基因突变和临床特征。
Results The buspirone can significantly improve the ataxia of patients with stroke compared with the controls(P<0.01). 结果治疗组在平衡性和协调性方面与对照组比较有明显改善(P<0.;01)。
Conclusion:The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia. 结论:遗传性共济失调的发生、发展可能与该区域点突变无关。
We report two brothers with a progressive cerebellar syndrome due to spinocerebellar ataxia type 8 (SCA8). 我们报告了两个患有渐进性小脑综合征的兄弟，是由于8型脊髓小脑共济失调(SCA8)所致。
Objective To explore the clinical and molecular biological characteristics of spinocerebellar ataxia type 3 (SCA3). 摘要目的探讨脊髓小脑性共济失调(SCA)3型的临床与分子生物学特征。