英语释义

• inability to coordinate voluntary muscle movements; unsteady movements and staggering gait

片语

involvement参与；牵连；包含；混乱；财政困难

vestibular ataxia前庭性共济失调

mix(Mix) （美、俄、巴）米克斯（人名）

intrapsychic ataxia内心运作失调

confusion混淆，混乱；困惑

enzootic ataxia羔羊地方性运动失调

Friedreichs ataxia弗里德里希共济失调

family ataxia家族性共济失调

noothymopsychic ataxia翻译

Ataxia CP共济失调型

Ataxia UK共济失调慈善协会

chaos(Chaos)人名；(西)查奥斯

cerebellar ataxia[内科] 小脑性共济失调；小脑运动失调

disorder使失调；扰乱

英汉例句

• objective to investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.

  目的探讨共济失调毛细血管扩张癥的细胞遗传学异常特点。

• objective to study the gene mutation and clinical characteristics of hereditary spinocerebellar ataxia type 7 (sca7).

  目的研究中国人遗传性脊髓小脑型共济失调（sca）7型（sca7）的基因突变和临床特征。

• 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。

• objective to analyze the role and location of ubiquitin-dependent proteolysis pathway(upp) in pc12 cells transfected by plasmids with spinocerebellar ataxia type 3(sca3) gene.

  目的分析泛素依赖的蛋白水解通路（upp）在转染了脊髓小脑性共济失调3型（sca3）基因的pc12细胞中的定位及作用。

• 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癥状的临床疗效。

• objective to study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (sca7).

  目的研究遗传性脊髓小脑性共济失调7型（sca7）的基因突变和临床特征。

• objective to study the clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7 ( sca7) .

  目的研究中国人遗传性脊髓小脑型共济失调7型（sca7）的临床和分子生物学特征。

• sural amplitude was negatively correlated with disease duration and ataxia score.

  腓肠神经的幅度与疾病持续时间、共济失调评分呈负相关。

• 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。

• in addition, research studies have shown that this enzyme is deficient in the mitochondrial disease friedreich's ataxia (4,5).

  此外研究表明，在一种名为弗立特里希氏共济失调的线粒体病中该酶有缺失（4，5）。

• objective to study the possible relationship between mitochondrial dna point mutations and hereditary ataxia (ha).

  目的研究线粒体dna点突变与遗传性共济失调（ha）的关系。

• methods the length of genetic segment of sca1, sca2 and sca3 in 92 patients with ataxia of unknown origin were detected by polymerase chain reaction (pcr) and agarose gel electrophoresis .

  方法应用pcr方法和琼脂糖凝胶电泳对92例不明原因共济失调先证患者测定其sca1、sca2和sca3基因片段长度。

• methods the clinical datas of 36 infant patients suffering from acute ataxia are analyzed retrospectively.

  方法对36例急性共济失调患儿的临床资料进行回顾性分析。

• objectiveto investigate the efficacy of acupuncture in ataxia children with cerebral palsy.

  目的探讨针刺疗法治疗共济失调型脑瘫的疗效。

• objective to study the molecular genetic diagnosis and clinical cha ra cteristics of spinocerebellar ataxia type 7 (sca7).

  目的研究分析脊髓小脑性共济失调7型（sca7）的分子遗传学诊断、应用以及临床表现特征。

• in the 129mv subtypes, psychiatric signs were often associated with parkinsonism, followed by ataxia and myoclonus, whereas aphasia was rare.

  在129mv中，精神病表现经常伴随震颤麻痹，随后为运动失调和肌阵挛，而失语癥罕见。

• hypotension may occur as a symptom of overdose with signs of apathy and ataxia .

  低血压可能发生，作为与冷漠和共济失调癥状过量的迹象。