基本释义:

小脑性运动失调

网络释义

1)cerebellar ataxy,小脑性运动失调

2)Mariess ataxia,遗传性小脑性运动失调

3)cerebellar ataxia,小脑运动失调

4)Cerebellar ataxia,小脑性共济失调

5)locomotor ataxy,运动性运动失调

6)kinetic ataxy,动力性运动失调

用法和例句

Consciousness disorders and cerebellar ataxia in one patient induced by large dose oral administration of carbamaze-pine;

大剂量服用卡马西平出现意识障碍、小脑性共济失调1例

The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed.

回顾小脑性共济失调的研究历史、分类,介绍脊髓小脑共济失调的病因机制和治疗方法。

GluRδ2 deficiency or mutations cause ataxia which is very similar to cerebellar ataxias.

背景:小脑性共济失调是一组具有高度临床和遗传异质性的神经系统退行性疾病。

acute cerebellar ataxia

急性小脑性共济失调

spinocebellar ataxia

脊髓小脑性共济失调

Systematic Review of Spinocerebellar Ataxias and Clinical Study of Spinocerebellar Ataxias in the Three Gorge Reservoir Area

脊髓小脑性共济失调系统评价和三峡库区脊髓小脑性共济失调临床研究

Clinical experiences on acupuncture for treatment of cerebellar ataxia after stroke

针灸治疗中风后小脑性共济失调的临床体会

The Molecular Mechanism of Hereditary Cerebellar Ataxia in Waddles Mouse;

Waddles小鼠遗传性小脑性共济失调的分子机制的研究

The Clinical Features and Molecular Biology Studies on Hereditary Spinocerebellar Ataxia Type 3 in Ningxia Area

宁夏地区遗传性脊髓小脑性共济失调3型的临床与分子研究

Minimum prevalence of spinocerebellar ataxia 17 in the north east of England

英格兰东北部17型脊髓小脑性共济失调的最低患病率

The Study of Genetic Diagnosis and Mitochondrial DNA Partly Mutations in Spinocerebellar Ataxia Type 3;

脊髓小脑性共济失调3型的基因诊断与线粒体DNA部分突变的研究

Analysis and Application of Spinocerebellar Ataxia Type 1、2(SCA1、SCA 2) Gene and Mitochondrial DNA Partly Mutations in SCA1、SCA 2;

脊髓小脑性共济失调1、2型基因检测分析与线粒体DNA突变的研究

Mutational Analysis of Glutamate Receptor Delta 2 Gene (GluR δ2) in Patients with Cerebellar Ataxia

小脑性共济失调症患者谷氨酸受体δ2基因突变研究

Gene Diagnosis and CAG Repeat Analysis of Spinocerebellar Ataxia Cases of Guangxi Region

脊髓小脑性共济失调病人的基因诊断和CAG重复扩增研究

Mutational Study of Exon 12 of Glutamate Receptor δ2 Gene in Patients with Cerebellar Ataxia

小脑性共济失调症患者谷氨酸受体δ2基因12号外显子突变研究

Molecular Genetic Diagnosis and Clinical Analysis of Characteristics of Spinocerebellar Ataxia Type 2

脊髓小脑性共济失调2型的分子遗传学诊断及临床分析

Analysis and Application of Spinocerebellar Ataxia Type 1、2、3 Gene and Mitochondrial DNA Partly Mutations in SCA1、SCA2、SCA3

脊髓小脑性共济失调1、2、3型基因检测分析与线粒体DNA突变的研究

The Research of Clinical Features and Gene Mutation of Five Families with Spinocerebellar Ataxia in Shangdong

山东地区脊髓小脑性共济失调5个家系的临床表现和基因突变分析

Cerebellar ataxia model and pathology in rats

大鼠小脑共济失调模型及病理学研究

Hereditary Cerebellar Ataxia Treated by Ganoderma capsense(Lloyd)Teng,A Report of 4 Cases

薄树芝制剂治疗遗传性小脑共济失调——附4例报告

Population based study of late onset cerebellar ataxia in south east Wales

威尔士东南部地区一项关于迟发型小脑共济失调的人群调查研究