ataxia
美 [əˈtæksiə] 
英 [ə'tæksiə]
英汉双解
1. | 共济失调，运动失调（表现为动作不稳、不协调）the loss of full control of the body's movements |
英汉解释
英英解释
例句
Conclusion: The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia.
结论：遗传性共济失调的发生、发展可能与该区域点突变无关。
Crazy The chicks show an ataxia not unlike the ataxia of vitamin E deficiency known as encephalomalacia or crazy chick disease.
雏鸡显示共济失调，但与维生素E缺乏的称为小脑软化症或疯狂病
Objective To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS.
目的探讨感觉性共济失调型CIDP的临床特点和发病机理。
Objective: To investigate the clinical features of an autosomal recessive inherited ataxia pedigree and exclude known causal genes.
目的：探讨常染色体隐性遗传性共济失调家系的临床特征并排除已知的致病基因。
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。
Physical examination revealed a lethargic patient with ophthalmoplegia, ataxia, and hyporeflexia.
体检表明，与眼肌麻痹，共济失调昏昏欲睡耐心，反射低下。
and endolymphatic sac tumors. Cerebellar hemangioblastomas may be associated with headache, vomiting, and gait disturbances or ataxia.
小脑成血管细胞瘤可能表现为头痛，呕吐，步态失调或共济失调。
We suggest that cerebellar ataxia may be characterized by defective feedforward control.
我们认为，可能是小脑性共济失调的特点是有缺陷的前馈控制。
abstract: Objective: To investigate the therapeutic effect of scalp-plus body-acupuncture on cerebellar ataxia.
目的：观察头针结合体针治疗小脑性共济失调的疗效。
Normally involved in the response to stress and repair of DNA, ATM is mutated in the rare genetic disorder ataxia-telangiectasia (AT).
ATM正常情况下参与应激反应和DNA修复，在罕见的遗传性紊乱疾病--共济失调性毛细血管扩张症（AT）中，ATM发生变异。
Conclusion Short-term treatment with buspirone can improve the ataxia symptoms after stroke.
结论丁螺环酮短期内可有效改善脑卒中后共济失调症状。
When they arise in the cerebellum, ataxia and headaches secondary to compression of the fourth ventricle and hydrocephalus are common [3].
当发生在小脑半球时，继发于四脑室受压和脑积水的头痛及共济失调是常见的。
The results indicate that the two sides of welding joint is ataxia, and the dehiscence occurs.
结果表明，焊接缝的两边不整齐，并且有开裂的现象。
Knuckling at fetlocks, ataxia, tail deviation and tail may be flaccid.
扣打距毛，运动失调，尾偏斜和尾可能松垂。
Methods To Summarize clinical data of 16 cases with sensory ataxia form of GBS.
方法总结16例以深感觉障碍为主要表现的CIDP患者的临床资料。
Conclusion: Scalp-plus body acupuncture has a marked therapeutic effect on cerebellar ataxia.
结论：头针结合体针治疗小脑性共济失调疗效明显。
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。
Results The buspirone can significantly improve the ataxia of patients with stroke compared with the controls(P01).
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（P0.01）。
Objective To summarize the common types and medical reasons for acute infant ataxia.
目的总结小儿急性共济失调的常见类型与病因。
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。
The patient improved rapidly although the ataxia persisted.
病人迅速好转，但仍然存在的共济失调。
Conclusion Avermectine may cause ataxia by disturbing the activity of nerve metabolism enzyme in rats.
结论阿维菌素可以造成小脑内神经代谢酶活力改变而引起运动失调。
Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia.
目的探讨遗传性脊髓小脑型共济失调（SCA）病人SCA3基因突变的意义。
Objective To explore the clinical and molecular biological characteristics of spinocerebellar ataxia type 3 (SCA3).
目的探讨脊髓小脑性共济失调（SCA）3型的临床与分子生物学特征。
also muscle Array twin, hyperreflexia, sweating, shivering, tremor, diarrhea, ataxia, fever and so on, life-threatening.
反射亢进、出汗、寒战、震颤、腹泻、共济失调、发热等，威胁生命。
Objective To observe the effect of buspirone on ataxia symptom after stroke.
目的观察丁螺环酮对改善脑卒中后共济失调症状的临床疗效。
difficult to hand pick up small objects, the lack of thumb to index finger pinch action athetosic, ataxia, mixed with action and so on.
用手拾小物件困难，缺乏拇指食指夹捏动作，手足徐动、共济失调、拌动等。
Objective: To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia.
前言：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 possible relationship between mitochondrial DNA (mtDNA) and hereditary ataxia (HA).
目的探索线粒体DNA点突变与遗传性共济失调的关系。
A study of clinical analysis and genetic polymorphism in hereditary spinocerebellar ataxia with psychiatric symptoms
遗传性共济失调伴精神障碍的临床及遗传研究
clinical observation on point - through - point acupuncture for treatment of cerebellar ataxia after apoplexy
透穴刺法治疗中风后小脑性共济失调临床观察
Aberrance analysis of mitochondrial DNA in a family with hereditary ataxia in Guangxi province
遗传性共济失调一家系中发现的线粒体DNA突变
Research on clinical characteristics and ATM gene mutations in Chinese patients with ataxia-telangiectasia
共济失调毛细血管扩张症两例患者临床与ATM基因突变研究
Establishment of germplasm repository of spinocerebellar ataxia
脊髓小脑性共济失调遗传种质库的建立
Rehabilitative evaluation and treatment for patient with cerebellar ataxia
小脑性共济失调患者的康复评定与治疗
The clinical characteristics and nursing measures of children with acute cerebellar ataxia
小儿急性小脑炎的临床特点和护理
Observation on Therapeutic Effect of Point-through-Point Therapy on Cerebellar Ataxia After Stroke
透穴刺法治疗中风后小脑共济失调的疗效观察
The Treatment of Cerebellar Ataxia with Buspirone Hydrochloride
丁螺环酮治疗小脑性共济失调
Mitochondrial DNA point mutations studies in hereditary ataxia
线粒体DNA部分点突变与遗传性共济失调的关系研究
Molecular genetic diagnosis and clinical characteristics of spinocerebellar ataxia type 6
脊髓小脑性共济失调6型的分子遗传学诊断及临床特点
