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- paramyotonia ataxia [医] 共济失调性肌强直病
- 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。
- 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。
- 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。
- Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia. 目的探讨遗传性脊髓小脑型共济失调(SCA)病人SCA3基因突变的意义。
- 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。
- The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed. 回顾小脑性共济失调的研究历史、分类,介绍脊髓小脑共济失调的病因机制和治疗方法。
