该词条未找到_海词词典

您要查找的是不是：

olivopontocerebellar ataxia 橄榄-脑桥-小脑共济失调
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。
Objective:To explore an MRI quantitative diagnostic standard for olivopontocerebellar atrophy(OPCA). 目的:探讨橄榄桥脑小脑萎缩的MRI量化诊断标准。
Objective To evaluate the diagnostic value of SPECT rCBF imaging in examining patients with olivopontocerebellar atrophy(OPCA). 目的评价SPECT脑血流灌注显像在橄榄桥脑小脑萎缩(OPCA)诊断中的价值。
Objective: To investigate the clinical manifestation and neuroimaging characteristic of olivopontocerebellar atrophy ( OPCA) . 目的:探讨橄榄脑桥小脑萎缩(OPCA)的临床和影像学特点。
Abstract: Objective To evaluate the diagnostic value of SPECT rCBF imaging in examining patients with olivopontocerebellar atrophy(OPCA). 文摘:目的评价SPECT脑血流灌注显像在橄榄桥脑小脑萎缩(OPCA)诊断中的价值。
Olivopontocerebellar atrophy (OPCA) is a term used to define neuronal degeneration in the cerebellum, pontine nuclei, and inferior olive. 什麽是'橄榄桥脑小脑萎缩-罕见的神经系统紊乱'?
Objective: To investigate the clinical manifestation and neuroimaging characteristic of olivopontocerebellar atrophy (OPCA). 摘要目的：探讨橄榄脑桥小脑萎缩(OPCA)的临床和影像学特点。
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)。