motor ataxia
- motor ataxia的基本解释
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运动性共济失调
- 更多网络例句与motor ataxia相关的网络例句 [注：此内容来源于网络，仅供参考]
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Patients' symptoms were assessed in accordance with Unified Parkinson's Disease Rating Scale (partsⅠ,Ⅱ,Ⅲ,Ⅳ were respectively used to evaluate mental activity, activities of daily living, motor nerve characteristics, complication therapy), International Cooperative Ataxia Rating Scale (including gait, cooperative ataxia, dysarthrosis, ocular dyscinesia), Activities of Daily Living Scale and mini-mental state examination.
分别于移植前及移植后2个月，采用统一帕金森病评定量表（partⅠ、Ⅱ、Ⅲ、Ⅳ分别评价心理活动、日常生活活动、运动神经特性、并发症的治疗）、国际共济失调量表（包括姿势步态、肢体共济失调、构音障碍、眼球运动障碍4项因子）、日常生活能力量表、简易智力量表对患者临床症状的变化进行评定。
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To investigate the gene mutation of clinical and neuroelectrophysiological characteristics in Machado-Joseph disease. The gene mutation was detected in 45 patients diagnosed as spinocerebellar ataxia and 30 "healthy relatives". Brain stem evoked potentials, visual evoked potentials and motor conduction velocity and sensory conduction velocity were performed on MJD.
为了解Machado-Joseph病基因突变及临床的神经电生理特点，对16个诊断为遗传性小脑性共济失调家系的45例病人及30例家系的&正常&人作MJD基因突变分析，检出MJD基因的病人行肢体运动及感觉神经传导速度、脑干诱发电位，视觉诱发电位的检查。
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Primary brain stem tumours were located mainly in the pons (91.7%).The multiple cranial nerve palsies, cerebellar ataxia, motor and sensory disturbanceswere the dominant objective findings.
临床特征除多数颅神经麻痹、锥体束和脑干小脑联系纤维功能障碍外，尚有括约肌障碍、不自主发笑和肌阵挛发作等。