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involuntary movement
相关语句
  不自主运动
     ③ Score of abnormal involuntary movement scale: At the ends of the 4th and 8th weeks in the clozapine group, it was significantly higher in smokers than in nonsmokers (t=2.093, 2.101, P < 0.05).
     ③不自主运动评分:氯氮平组非吸烟者在第4周末、第8周末显著高于吸烟者(t=2.093,2.101,P<0.05)。
短句来源
     [Results] Pulsatile treatment with Levodopa induced contralateral forelimb, trunk and orofacial abnormal involuntary movement(AIM) in PD rats , similar to LID in PD patients.
     结果LID大鼠模型复制成功后出现了与人类LID相似的对侧上肢、躯干和口面部异常不自主运动(AIM),并随左旋多巴治疗时间的延长而加重。
短句来源
     Results After treatment with SCH23390,abnormal involuntary movement(AIM) in LID rats was decreased and the changes of expression of NGFI-β mRNA in striatum were not significant.
     结果SCH23390治疗后,LID大鼠异常不自主运动明显减少,而氟哌啶醇治疗后则无明显改变。
短句来源
     The clinical presentation is as follows: unconsciousness and uncontrolled urine or motion(6 cases), intracranial hypertension (4 cases), tic or decerbrate rigidity (3 cases), disorder of intelligence (3 cases), central fever (2 cases ); hemiplegia or quadriplegia (2 cases)), psychosis and involuntary movement (1 case).
     临床表现为意识障碍及尿便失禁(6例),高颅压(4例),抽搐或去脑强直(3例),智能障碍(3例),中枢热(2例),偏瘫或四肢瘫(2例),精神症状及不自主运动(1例)。
短句来源
     Conclusions: TD formation rate is high,The predilection site is the tongue、lip and mouth,2/3 patients abnormal involuntary movement does not affect the normal movement,also does not perceive.
     TD的相关因素分析发现首发年龄越小、病程越长、合用安坦四肢不自主运动有加重趋势。 结论:TD发生率较高,好发于舌部、唇和口周部,2/3的病人异常不自主运动对正常运动没有影响且觉察不到。
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  不随意运动
     After comparing the clinical symptoms and physical signs between the analogous apoplexy group and apoplexy one, using American SAS statistical analysis soft ware to take logistic regression analysis on 2206 cases, combining with clinical practice, bibliography investigation and specialists' experience, the main symptoms of analogous apoplexy were defined as: vertigo, sensory disturbance, severe headache, visual abnormality, involuntary movement, mental aberration, epileptic attack, agnosia, alexia and agraphia, etc.
     运用类中风组与中风组临床症状体征对照的研究方法 ,采用美国SAS统计分析软件 ,对 2 2 0 6例调研资料进行logistic回归分析等多因素分析。 参考回归结果 ,并结合临床实际、文献调查、专家经验 ,从而确定了类中风的主症为 :眩晕 ,身体感觉障碍 ,剧烈头痛 ,视物异常 ,不随意运动 ,精神障碍 ,癫痫样发作 ,失认失读失写等。
短句来源
     Conclusion PKD was characterized by movement induced,transient,local or generalized involuntary movement,and belonged to channelopathy. Antiepileptic drugs,particularly carbamazepine,were effective to PKD.
     结论发作性运动诱发性运动障碍病是一种由运动诱发的、短暂的、发作性局部或全身不随意运动,属于离子通路疾病,用抗癫药疗效好。
短句来源
  “involuntary movement”译为未确定词的双语例句
     Results After administration of antisense FosB, scores of abnormal involuntary movement (AIM) was decreased in LID rats (12.5±5.4 vs 40.1±9.2,P<0.01).
     结果反义FosB治疗前后LID大鼠AIM评分分别为40.1±9.2、12.5±5.4,差异有统计学意义(P<0.01)。
短句来源
     Methods: All patients with schizophrenia were assessed for TD by the Abnormal Involuntary Movement Scale (AIMS).
     方法:使用异常不自主运动量表(AIMS)评定SCH患者有无TD及TD的严重程度,并采用简明精神病评定量表(BPRS)评定患者临床精神症状;
短句来源
     Effect of MK801 on neuronal activity in the basal ganglia in a rat model of PD with levodopa-induced abnormal involuntary movement
     MK-801对左旋多巴诱导异动症大鼠模型基底节区神经元活性的影响
短句来源
     Method:Diagnosis of tardive dyskinesia(TD) and the identification of TD severity was assessed by the abnormal involuntary movement scale (AIMS).
     方法:使用异常不自主运动量表(AIMS)评定有无TD及其严重程度。
短句来源
     Results The mice in the ganoderma spores oil+MPTP group presented significantly less involuntary movement of the limbs in the pole test than the mice in MPTP group.
     结果(1)爬杆实验中肢体出现刻板抖动行为的小鼠数目比例灵芝孢子油+MPTP组较MPTP组显著减少(12.5%vs68.7%)。
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  involuntary movement
Among TD patients, we found no significant correlation between COMT genotypes and the total scores of abnormal involuntary movement scale (AIMS) (p=0.629).
      
With in the TD group, we could not discover a significant correlation between NOS1 3'-UTR C276T genotypes and the scores of abnormal involuntary movement scale (AIMS) (p=0.219 and 0.774).
      
TS has long been regarded an involuntary movement disorder.
      
The subjects were rated on the Abnormal Involuntary Movement Scale (AIMS) and the Dyskinesia Identification System: Condensed User Scale (DISCUS) by trained raters.
      
Monotherapy with subcutaneous regular insulin induced a progressive normalisation of glycaemia as well as a parallel improvement of the abnormal involuntary movement scale on a nine-day sequential observation.
      
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Three cases of focal epilepsy in nonketotic hyperglycaemia are presented in this paper.These seizures manifested not only focal convulsion of face or limb, but also choreoid or athetoid involuntary movements. That hepatitis might cause epilepsy was not supported. Antiepileptic therapy was not effective for this disorder, but the effect of antihyperglycaemic agent such as insulin was favourable.

报告无酮性高血糖性局限性癫痫三例。癜痫发作除表现为局限性颜面或个别肢体抽搐外,还可表现为舞蹈样或手足徐动样不自主运动发作。肝炎致癫作用未得到支持。本病用抗癫痫药物治疗无效,对降糖药物反应良好。

Paroxysmal kinesigenic choreoathetosis (PKCA) is a rare nonprogressive involuntary movement disorder induced by movement or startle.The movements are tonic,dystonic or choreoathetotic. Onset occurs most often during childhood Four cases of the PKCA (2 familial form and two sporadic form) were reported All of them had attacks after the initiation of movements, such as rising from chair running, etc. Results of physical examination, laboratory studies, EEGs and CT scans of the head were...

Paroxysmal kinesigenic choreoathetosis (PKCA) is a rare nonprogressive involuntary movement disorder induced by movement or startle.The movements are tonic,dystonic or choreoathetotic. Onset occurs most often during childhood Four cases of the PKCA (2 familial form and two sporadic form) were reported All of them had attacks after the initiation of movements, such as rising from chair running, etc. Results of physical examination, laboratory studies, EEGs and CT scans of the head were normal in all patients.The attacks ceased in two of the four patients after treatment with phenytoin.

阵发性运动源性舞蹈手足徐动症(PKCA)是一种罕见的非进展性不自主运动疾病。发作时常表现为痉挛样、肌紧张异常样或舞蹈手足徐动样,而且常由突然运动或惊跳所诱发。发病年龄以儿童期为多见。本文报道4例PKCA,2例有家族史而另2例为散发者,4例均由突然运动如由坐位起立、跑步等所诱发。发作间歇期神经系统检查,实验室检查,不同时期脑电图(包括诱发试验)和脑CT扫描等均未发现异常。经苯妥英钠治疗后2例发作被完全控制,另2例则无效。

Paroxysmal kinesigenic choreoathetosis(PKCA)is a rare involuntary movement disorder. Attacks are induced by movemen or startle. The movements are tonic, dystonic or choreoathetotic. Sporadic or more commonly familial cases have been reported. Onset occurs most often during childhood and the course is nonprogressive. Response to anticonvulsant therapy is usually excellent. In this paper, four cases (2 in familial form and two in sporadic form) were reported. The attacks in all these 4 patients were...

Paroxysmal kinesigenic choreoathetosis(PKCA)is a rare involuntary movement disorder. Attacks are induced by movemen or startle. The movements are tonic, dystonic or choreoathetotic. Sporadic or more commonly familial cases have been reported. Onset occurs most often during childhood and the course is nonprogressive. Response to anticonvulsant therapy is usually excellent. In this paper, four cases (2 in familial form and two in sporadic form) were reported. The attacks in all these 4 patients were induced by sudden movements, such as rising from the chair. on running and so on. Physical examinations and laboratory studies including EEGs and CT scans of the head were entirely negative in all 4 patients. The attacks ceased in two of four patients after the treatment with phenytoin.

阵发性运动源性舞蹈手足徐动症是一种比较罕见的异常运动发作,其发作呈强直样、扭转痉挛样或舞蹈手足徐动样,可被突然运动或惊跳所诱发,不伴意识障碍,可有家族史或为散发。本文报道4例并结合文献复习对其临床特点、分类、可能之病理生理机制、有关鉴别诊断及治疗等进行了简要阐述。

 
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