ataxic
These signs are followed by ataxia.
这些症状之后就是共济失调。
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。
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%,明显优于对照组(76%)。
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；
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。
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
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
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。
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。
Results Both types of reversing prisms can induce obvious ataxia and motion sickness symptoms.
与秋千诱发运动病症状比较,倒视诱发运动病症状较轻，出现较缓慢;
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。
The chicks show an ataxia not unlike the ataxia of vitamin E deficiency known as encephalomalacia or crazy chick disease.
雏鸡显示共济失调，但与维生素E缺乏的称为小脑软化症或疯狂病（crazy chick disease）不同。
It is also caused by mutations in genes associated with autosomal dominant cerebellar ataxia (ADCA), notably CAG/CAA repeat expansions in SCA2.
它还可能由常染色体显性遗传性小脑性共济失调相关基因突变引起，尤其是SCA2中的CAG/CAA重复扩增。
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。
Conclusion: clinical and electrophysiological feature were one of diagnostic criterial of sensory ataxia form Guillain-Barre Syndrome.
结论：临床及电生理特点可作为感觉性共济失调型格林-巴利综合征的诊断标准之一。
Objective:To investigate the clinical features of an autosomal recessive inherited ataxia pedigree and exclude known causal genes.
目的:探讨常染色体隐性遗传性共济失调家系的临床特征并排除已知的致病基因。
The authors describe the case of a 45-year-old man with progressive gait ataxia and sensorimotor deficits of the upper and lower extremities.
作者描述了一例45岁男性渐进性的步态共济失调和手足感觉运动缺陷患者。
Results:The incident rate of Involuntary Movements is 4%,Most of which are tremor and chorea,and a few of which are ataxia and myoclouns .
结果:森林脑炎病人伴发不自主运动发生率为4%,以震颤、舞蹈动作为主,少数为共济运动障碍及肌阵挛。
Described in 1881 by the German neurologist Nicolas Friedreich, Friedreich's Ataxia is a progressing neurological disease.
我一个德国朋友得了这种病,病症如下,请各位帮忙看看在中国能否治疗,谢谢:
Since nystagmus and gait ataxia do not distinguish between the central or peripheral causes of vertigo, AICA infarct could masquerade as peripheral vestibular lesions.
由眼球震颤和步履运动失调无法区分中枢性或周边性之晕眩症，因此前下小脑动脉梗塞与周边前庭病变可产生临床相似的症状。
Objective The purpose of the investigation was to explore the relationship between ataxia telangiectasia(AT) gene mutation and esophagus cancer as well as colon cancer.
目的：探讨共济失调毛细血管扩张症(AT)基因突变与食管癌及结肠癌发病的关系。
The total response rates were similar, and the side effects of clonazepam were fatigue, dizzziness, ataxia, and atonia, while that of chlorpromazine were drowsy and EPS.
氯硝西泮副反应以困倦乏力、头晕、食欲减退、共济失调、肌张力减退多见,其发生率与氯丙嗪组相比无显著差异。
Methods:Fragment analysis based on CEQ8000 sequencer were applied to analyze the CAG repeat of SCA1 gene in two autosomal dominant inherited spinocerebellar ataxia pedigrees.
方法:采用基于CEQ8000核酸分析仪的片段分析方法对2个表型为常染色体显性遗传脊髓小脑共济失调家系进行SCA1基因CAG重复序列突变检测,并分析其临床特征。
Tzu Chi volunteer Cai Caizhong from Kaohsiung contracted spinocerebellar ataxia two years ago.The disease gradually destroys his ability to move and talk.
住在高雄的慈济志工蔡财忠两年前被发现罹患小脑萎缩症，语言能力以及行动开始退化；
If cericalertigoexists outside these experimental conditions, it is obiously characterized by ataxia and unsteadiness of gait, and not by a clear rotational or linear ertigo.
如果颈性眩晕在实验条件以外存在，它会明显的以共济失调和步态失稳为特征而不是以明显的旋转性或线性的眩晕为特征。
Objective:To investigate the clinical features of the cases with intermediate Cytosine-Adenine-Guanine(CAG) repeat alleles of spinocerebellar ataxia type 1(SCA1).
目的:探讨脊髓小脑共济失调1型(SCA1)中等重复动态突变患者临床表型特征。
He was transferred to our rehabilitation ward 36 days after the heat stroke injury due to ataxia, dysarthria, poor emotional control, and a personality change.
病人在病发第36天，因运动失调、呐吃、情绪不易控制、性格改变等问题，转到本院复健科。
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。
Its symptoms include sensory impairment in the distal limbs, ataxia, tremor, and pinch weakness.Electrophysiology will show multiple neuropathies with distal involvement first.
病患的症状包括：肢体末端的感觉缺失，穿鞋子容易掉，手脚麻木像戴手套穿脚袜一般，拿小东西会掉，走路不稳；
Pyramidal involvement, cerebellar ataxia and urinary disturbances are common. Less frequent findings include sleep disorders and dysautonomia. Fluctuations may occur.
常见的有锥体系受累、小脑性共济失调和排尿困难。次常见的包括睡眠障碍和家族性自主神经机能异常。可能会出现症状波动。
Producted by the company.It has the necessary aminophenol without which the person's muscle growth will be blocked and the person will have ataxia and anaemia.
味之素莲花氨基酸有限公司出品,必需氨基酸，人体缺乏时会影响肌体生长发育，引起神经障得、运动失调、贫血等。
The results showed that the plasma level of PGE2 in ataxic chicks were significantly higher than that of healthy ones. T he data suggest that immunological function of chicken with nutritional encephal omal- acia reduce.
结果表明,脑软化雏鸡血浆中PGE2含量较健康对照组雏鸡显著增高(P
He began to feel the symptoms of a nerve disease called ataxia which interfered with his movements and made it difficult for him to hold a brush and manipulate paint with his usual ease.
他开始感到一种症状--运动性共济失调的神经性疾病，这种病症影响了他的行动功能，使他很难握住画笔，不能像以往那样遂心所欲地驾驭绘画。
Clinical symptoms associate cerebellous ataxia, pyramidal syndrome with Babinski sign , abolition of reflexes, disorder of profound sensitivity, dysarthria, oculomotor disorders and cardiomyopathy.
临床症状伴有：小脑共济失调，椎体综合征，如巴宾斯基阳性，反射消失，深度反应失调，构音障碍，眼球运动障碍，以及原发性心肌疾病。
In contrast, similar-sized but uninterrupted repeats were associated with ADCA in which cerebellar ataxia was constant and associated only rarely with one or more mild parkinsonian signs.
与之相反，大小类似但未阻断重复与ADCA相关，这些患者小脑性共济失调持续存在而且只与一个或多个中等帕金森体征相关。
The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed. The pathogenesis and treatments of spinocerebellar ataxia were summarizd.
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。