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ataxia相关的网络例句

查询词典 ataxia

与 ataxia 相关的网络例句 [注:此内容来源于网络,仅供参考]

Abasia due to ataxia of the legs.

由于腿的共济失调而不能走路。

Analyse and evaluate the practicability and clinical value of International Cooperative Ataxia Rating Scale in ataxia patients.

分析并评价国际协作共济失调评估量表对共济失调患者的实用性和临床价值。

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不同。

The chick s 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不同。

Headache, vomiting, ataxia, and visual deterioration are common presenting symptoms. Hemiataxia is a frequent finding in adults because of the hemispheric location of most tumors. Gait ataxia, papilledema, nystagmus, facial palsy, and neck stiffness are also common.

头痛、呕吐、共济失调以及视力减退是常见的临床表现,成人常出现偏身共济失调,这是由于肿块多位于小脑半球,步态共济失调、视乳头水肿、面瘫、颈项强直也是常见的。

The addition of puerarin, tea polyphenol and acid compositions in VECO effectively improved the effects on soberness, intoxication avoiding, ataxia correcting and memory barrier eliminating. The tea polyphenol has superior behavior on soberness, intoxication avoiding and memory barrier eliminating than that of puerarin, while puerarin is more effective in the function of ataxia correcting than tea polyphenol.

金葛露中加入葛根素、茶多酚和酸类物质有助于解酒、防醉、纠正运动失调和改善记忆障碍,其中茶多酚的解酒、防醉和改善记忆障碍的效果比葛根素明显,葛根素纠正运动失调作用的效果比茶多酚明显。

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。

We investigated the clinical features and gene mutation in a pedigree of spinocerebellar ataxia.

对一脊髓小脑性共济失调(Spinocerebenllar ataxia, SCA)家系的患者进行临床特征及相关基因突变研究。

Objective To investigate the related factors of International Cooperative Ataxia Rating Scale score on spinocerebellar ataxia type 3 (SCA3) patients.

目的探讨国际协作共济失调评估量表评估脊髓小脑共济失调3型患者的相关因素。

Spinocerebellar ataxia is an autosomal dominant hereditary neuron disorder disease.

脊髓小脑萎缩症(Spinocerebellar ataxia, SCA)是一种体染色体显性的遗传性神经元退化性疾病。

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