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
