Novel Solution to Dynamic Economic Dispatch Considering Customer Interruption Costs Population based study of late onset cerebellar ataxia in south east Wales 计及用户停电损失的动态经济调度方法威尔士东南部地区一项关于迟发型小脑共济失调的人群调查研究
Population based study of late onset cerebellar ataxia in south east Wales 威尔士东南部地区一项关于迟发型小脑共济失调的人群调查研究
Cerebellar ataxia model and pathology in rats 大鼠小脑共济失调模型及病理学研究
The long-term prognosis should be guarded in the sense that patients can become very debilitated from the gait problems due to a combination of cerebellar ataxia and myelopathy. 关于长期预后,应该考虑到患者可能被小脑性共济失调和脊髓病变而致的步态异常折腾得身心俱疲。
Mutational Study of Exon 12 of Glutamate Receptor δ 2 Gene in Patients with Cerebellar Ataxia 小脑性共济失调症患者谷氨酸受体δ2基因12号外显子突变研究
Observation of the effects of Frenkel training in patients with cerebellar ataxia Frenkel训练法改善小脑性共济失调患者的疗效观察
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RamsayHunt综合征)进行探讨,以提高临床医师对其的认识。
MRI Findings of Hereditary Cerebellar Ataxia 遗传性小脑共济失调的MRI表现附2个家系报告
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。
The genetic disorder ataxia telangiectasia ( AT) is characterized by immunodeficiency, progressive cerebellar ataxia, gonadal abnormalities, radiosensitivity, and cancer predisposition. 基因缺陷所致共济失调-毛细血管扩张症(AT)表现为免疫缺陷、进行性共济失调、性腺发育异常、辐射敏感和易患癌症等。
The differential diagnosis between hereditary cerebellar ataxia and other systemic disorders were discussed, and pathological basis of this disease was described. 讨论了本病与其他疾病所致共济失调的鉴别诊断,以及本病的病理学基础。
The Treatment of Cerebellar Ataxia with Buspirone Hydrochloride 丁螺环酮治疗小脑性共济失调
Conclusions Frenkel training is effective to the patients of cerebellar ataxia, and can improve the ADL. 结论Frenkel训练法对改善患者的小脑性协调障碍有效,并能提高ADL水平。
Treatment of Cerebellar Ataxia Using Transplantation of Embryonic Cerebellum Suspensions: Experimental Research 胚胎小脑悬液移植治疗小脑共济失调的实验研究
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%。
Autoantibodies in postinfectious acute cerebellar ataxia 急性小脑性共济失调患者感染后出现自身抗体
The frequency of cerebellar ataxia, pyramidal bame signs, dysarthria and damages of automatic nervous system are 92.1%, 86.8%, 84.2% and 76.3% respectively. 2受累系统症状出现频率为小脑共济失调92.1%,锥体束征86.8%,构音障碍84.2%,自主神经损害76.3%。
Objective To observe the rehabilitation train ing effects of the Frenkel therapy on cerebellar ataxia. 目的观察Frenkel训练法对小脑性运动协调障碍患者的康复治疗效果。
Purpose To observe therapeutic effect of point-throuth-point therapy on cerebellar ataxia after stroke. 目的:观察透穴刺法治疗中风后小脑性共济失调的临床疗效。
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
Rehabilitative evaluation and treatment for patient with cerebellar ataxia 小脑性共济失调患者的康复评定与治疗
Late-onset pure cerebellar ataxia: Differentiating those with and without identifiable mutations 迟发性单纯小脑共济失调:鉴别有和无可识别突变的患者
Acute Cerebellar Ataxia: Clinical Analysis of 18 Cases 急性小脑性共济失调症18例临床分析
All patients had the symptom of vertigo and the signs of cerebellar ataxia. 所有患者均有眩晕及小脑性共济失调的症状体征;
A detailed physical examination shows cerebellar ataxia, lead pipe-like rigidity, positive pyramidal sign but orthostatic hypotension. 入院后查体有小脑性共济失调、肢体肌张力铅管样增高和锥体束征。
Background Fragile X-associated tremor-ataxia syndrome ( FXTAS) is a neurodegenerative disease characterized by progressive cerebellar ataxia and intention tremor. 背景脆性X相关震颤/共济失调综合征(fragileX-associatedtremor/ataxiasyndrome,FXTAS)是一种以意向性震颤和/或小脑性共济失调为主要特征的神经退行性疾病。
The onset age had no significant difference among each type. 2. The overlap of clinical features between the three SCA subtypes was broad, manifested as cerebellar ataxia and dysarthria. 各型的发病年龄无明显差别。2.临床表现相互重叠,临床表现主要以小脑性共济失调步态、构音障碍最常见、也是最早出现的临床症状。