ataxia
美 [??tæksi?] 
英 [?'tæksi?]
英漢雙解
1. | 共濟失調，運動失調（表現為動作不穩、不協調）the loss of full control of the body's movements |
英漢解釋
英英解釋
例句
Conclusion: The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia.
結論：遺傳性共濟失調的發生、發展可能與該區域點突變無關。
Crazy The chicks show an ataxia not unlike the ataxia of vitamin E deficiency known as encephalomalacia or crazy chick disease.
雛雞顯示共濟失調，但與維生素E缺乏的稱為小腦軟化癥或瘋狂病
Objective To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS.
目的探討感覺性共濟失調型CIDP的臨床特點和發病機理。
Objective: To investigate the clinical features of an autosomal recessive inherited ataxia pedigree and exclude known causal genes.
目的：探討常染色體隱性遺傳性共濟失調家系的臨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.
高鎂血癥的神經系統癥狀表現為肌肉無力、癱瘓、共濟失調、嗜睡和意識模糊。
Physical examination revealed a lethargic patient with ophthalmoplegia, ataxia, and hyporeflexia.
體檢表明，與眼肌麻痹，共濟失調昏昏欲睡耐心，反射低下。
and endolymphatic sac tumors. Cerebellar hemangioblastomas may be associated with headache, vomiting, and gait disturbances or ataxia.
小腦成血管細胞瘤可能表現為頭痛，嘔吐，步態失調或共濟失調。
We suggest that cerebellar ataxia may be characterized by defective feedforward control.
我們認為，可能是小腦性共濟失調的特點是有缺陷的前饋控制。
abstract: Objective: To investigate the therapeutic effect of scalp-plus body-acupuncture on cerebellar ataxia.
目的：觀察頭針結合體針治療小腦性共濟失調的療效。
Normally involved in the response to stress and repair of DNA, ATM is mutated in the rare genetic disorder ataxia-telangiectasia (AT).
ATM正常情況下參與應激反應和DNA修復，在罕見的遺傳性紊亂疾病--共濟失調性毛細血管擴張癥（AT）中，ATM發生變異。
Conclusion Short-term treatment with buspirone can improve the ataxia symptoms after stroke.
結論丁螺環酮短期內可有效改善腦卒中后共濟失調癥狀。
When they arise in the cerebellum, ataxia and headaches secondary to compression of the fourth ventricle and hydrocephalus are common [3].
當發生在小腦半球時，繼發于四腦室受壓和腦積水的頭痛及共濟失調是常見的。
The results indicate that the two sides of welding joint is ataxia, and the dehiscence occurs.
結果表明，焊接縫的兩邊不整齊，并且有開裂的現象。
Knuckling at fetlocks, ataxia, tail deviation and tail may be flaccid.
扣打距毛，運動失調，尾偏斜和尾可能松垂。
Methods To Summarize clinical data of 16 cases with sensory ataxia form of GBS.
方法總結16例以深感覺障礙為主要表現的CIDP患者的臨床資料。
Conclusion: Scalp-plus body acupuncture has a marked therapeutic effect on cerebellar ataxia.
結論：頭針結合體針治療小腦性共濟失調療效明顯。
Results Virus infection is the main cause resulted in acute ataxia in infant.
結果病毒感染是急性共濟失調的主要病因。
Results The buspirone can significantly improve the ataxia of patients with stroke compared with the controls(P01).
結果治療組在平衡性和協調性方面與對照組比較有明顯改善（P0.01）。
Objective To summarize the common types and medical reasons for acute infant ataxia.
目的總結小兒急性共濟失調的常見類型與病因。
It results in progressive ataxia beginning at a young age.
該疾病自幼犬期發病并導致漸進性共濟失調。
The patient improved rapidly although the ataxia persisted.
病人迅速好轉，但仍然存在的共濟失調。
Conclusion Avermectine may cause ataxia by disturbing the activity of nerve metabolism enzyme in rats.
結論阿維菌素可以造成小腦內神經代謝酶活力改變而引起運動失調。
Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia.
目的探討遺傳性脊髓小腦型共濟失調（SCA）病人SCA3基因突變的意義。
Objective To explore the clinical and molecular biological characteristics of spinocerebellar ataxia type 3 (SCA3).
目的探討脊髓小腦性共濟失調（SCA）3型的臨床與分子生物學特征。
also muscle Array twin, hyperreflexia, sweating, shivering, tremor, diarrhea, ataxia, fever and so on, life-threatening.
反射亢進、出汗、寒戰、震顫、腹瀉、共濟失調、發熱等，威脅生命。
Objective To observe the effect of buspirone on ataxia symptom after stroke.
目的觀察丁螺環酮對改善腦卒中后共濟失調癥狀的臨床療效。
difficult to hand pick up small objects, the lack of thumb to index finger pinch action athetosic, ataxia, mixed with action and so on.
用手拾小物件困難，缺乏拇指食指夾捏動作，手足徐動、共濟失調、拌動等。
Objective: To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia.
前言：目的：探索線粒體DNA點突變與遺傳性共濟失調的關系。
Objective: To study the possible relationship between mitochondrial DNA (mtDNA) and hereditary ataxia (HA).
目的探索線粒體DNA點突變與遺傳性共濟失調的關系。
A study of clinical analysis and genetic polymorphism in hereditary spinocerebellar ataxia with psychiatric symptoms
遺傳性共濟失調伴精神障礙的臨床及遺傳研究
clinical observation on point - through - point acupuncture for treatment of cerebellar ataxia after apoplexy
透穴刺法治療中風后小腦性共濟失調臨床觀察
Aberrance analysis of mitochondrial DNA in a family with hereditary ataxia in Guangxi province
遺傳性共濟失調一家系中發現的線粒體DNA突變
Research on clinical characteristics and ATM gene mutations in Chinese patients with ataxia-telangiectasia
共濟失調毛細血管擴張癥兩例患者臨床與ATM基因突變研究
Establishment of germplasm repository of spinocerebellar ataxia
脊髓小腦性共濟失調遺傳種質庫的建立
Rehabilitative evaluation and treatment for patient with cerebellar ataxia
小腦性共濟失調患者的康復評定與治療
The clinical characteristics and nursing measures of children with acute cerebellar ataxia
小兒急性小腦炎的臨床特點和護理
Observation on Therapeutic Effect of Point-through-Point Therapy on Cerebellar Ataxia After Stroke
透穴刺法治療中風后小腦共濟失調的療效觀察
The Treatment of Cerebellar Ataxia with Buspirone Hydrochloride
丁螺環酮治療小腦性共濟失調
Mitochondrial DNA point mutations studies in hereditary ataxia
線粒體DNA部分點突變與遺傳性共濟失調的關系研究
Molecular genetic diagnosis and clinical characteristics of spinocerebellar ataxia type 6
脊髓小腦性共濟失調6型的分子遺傳學診斷及臨床特點
