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- locomotor ataxia n. [医]脊髓痨;运动性共济失调
- Progressive locomotor ataxia 进行性运动性共济失调
- These signs are followed by ataxia. 这些症状之后就是共济失调。
- Kirov take off locomotor slowed down to match blimps. 基洛夫去掉了喷射器来适合其形象(肥气球).
- The components and functions of the locomotor system. 掌握运动系统的组成;
- 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。
- locomotor ataxy 运动性运动失调
- Investigations of Locomotor Capacity as a Model System, Annu. Rev. Ecol. Syst. 把运动能力作为一种模型系统的研究。
- 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。
- Locomotor Description: A motion charm that allows objects to be moved through the air. 一个移动咒,能使物体在空气中移动。
- Conclusion The correct function exercise,could promote effectively the function recovery of locomotor system dam... 结论:正确的功能锻炼,是促进运动系统损伤功能障碍康复的有效方法。
- Adenosine A(subscript 2A) receptors are selectively localized in basal ganglia and can affect the locomotor activity. 摘要腺苷A(下标2A)受体在基底神经节选择性表达并与运动行为有关。
- Functional outcome was measured using the Basso, Beattie, Bresnahan Locomotor Rating Score and footprint analysis. 通过Basso,Beattie,BresnahanLocomotor运动评分和足迹法分析,我们测定了它们的功能表现。
- 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。
- Both strong activity and mild activity were included in whole locomotor activity. 强活动和弱活动之和为总运动。
- 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。
- But no significant difference was found in the scores of locomotor function between the two groups(P>0.05). 将治疗组的运动功能评分与对照组相比较,差异无显著性意义(P>0.;05)。
- 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;