运动失调的

Clinical features were characterised by allolalia, dramatically indifference emotion,left agraphia , left ideomotor apraxia, alien hand syndrome, hemispatial neglect , gait apraxia, sensation and motion abnormality.

胼胝体病变的临床表现较复杂，10例患者分别表现有言语障碍、情感淡漠、左手失写、左手运动性失用、陌生手综合症、半侧空间忽略、步态失调、感觉和运动异常等。

At 14 postoperative days, the paralytic limbs'function of the survived rats were evaluated with the Ducker's method (grade 0: pamplegia grade 1: automatic action but could not support the body mass grade 2: could stand but could not walk grade 3: could walk but with difficulty and accompanied by spasm grade 4: could run accompanied by mild incoordination grade 5: normal movement).

术后14d将两组存活的实验鼠按Ducker's评级方法进行瘫痪肢体功能测定(0级：完全瘫；1级：能自主运动，但不能支撑体质量；2级：能站立但不能行走；3级：能行走，但困难伴痉孪；4级：能跑，但有轻度共济失调；5级：正常运动)。

Clinically, there may be a variety of similar to the performance of lacunar syndrome, such as pure athletic hemiparesis, pure sensory stroke, ataxia hemiparesis, dysarthria - clumsy hand syndrome, sensorimotor stroke and so on.

临床上可出现各种类似腔隙性综合征的表现，如单纯运动性轻偏瘫，单纯感觉性卒中，共济失调轻偏瘫，构音障碍——手笨拙综合征，感觉运动性卒中等。

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。

Results The clinical manifestations of TOBS comprised transient unconsciousness, vertigo, dyskinesia of eyeball, abnormality of pupils, dyskinesia of limbs, hemianopsia or cortical blindness, ataxia and memory impairment. MRI showed the local infarction in thalami, cerebellum, midbrain, pons, occipital lobe, temporal inner surface. The features of DSA were occlusion or stenosis in basilar artery and vertebral artery.

结果 TOBS的临床主要表现为一过性意识障碍、眩晕、眼球运动障碍及瞳孔的变化、肢体运动障碍、偏盲或皮质盲、共济失调及记忆功能损害；磁共振显示梗死灶在丘脑、小脑、中脑、脑桥、枕叶、颞叶内侧面；数字减影血管造影显示为基底动脉及椎动脉闭塞或狭窄。

Progressive supranuclear palsy is a degenerative neurological disorder of uncertain etiology characterized by gait ataxia, slowing or inability to generate voluntary saccadic eye movements, and axial rigidity.

译：进行性核上性麻痹是病因不明的神经系统退行性病变，临床表现为共济失调步态、自主眼球扫视运动无法完成或完成缓慢、躯干强直。

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。

Disorders of somatesthesia and locomotion and disturbance of mental function appeard when nerve tissue is injured .

神经组织损伤可造成患者躯体感觉，运动功能障碍和严重的心理功能失调。

Results The clinical manifestation for these cases are specifically showed as slow and deepen supply imbalance,pyramidon,pyramid bean and brain function injured disease status and eye-ball barrier,etc.

结果 临床突出特点为缓慢进行性加重的共济失调、锥体外系、锥体束、大脑高级功能受损症状及眼球运动障碍等。

Results The clinical manifestation for these cases are specifically showed as slow and deepen supply imbalance,pyramidon,pyramid bean and brain function injured disease status and eye-ball barrier,etc.

结果 临床突出特点缓慢进行性加重的共济失调、锥体外系、锥体束、脑高级功能受损症状及眼球运动障碍等。

It has been put forward that there exists single Ball point and double Ball points on the symmetrical connecting-rod curves of equilateral mechanisms.

从鲍尔点的形成原理出发，分析对称连杆曲线上鲍尔点的产生条件，提出等边机构的对称连杆曲线上有单鲍尔点和双鲍尔点。

The factory affiliated to the Group primarily manufactures multiple-purpose pincers, baking kits, knives, scissors, kitchenware, gardening tools and beauty care kits as well as other hardware tools, the annual production value of which reaches US$ 30 million dollars.

集团所属工厂主要生产多用钳、烤具、刀具、剪刀、厨具、花园工具、美容套等五金产品，年生产总值3000万美元，产品价廉物美、选料上乘、质量保证，深受国内外客户的青睐