1.
Cerebellar ataxia model and pathology in rats
大鼠小脑共济失调模型及病理学研究
2.
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
3.
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
4.
Experimental Study of Neural Stem Cells/Progenitors Transplantation on Spinocerebellar Ataxian Rat;
神经干/祖细胞移植治疗脊髓小脑共济失调大鼠的实验研究
5.
Research of Clinical Features and Gene Mutation of Patients with Spinocerebellar Ataxia Type 3 in Three Families;
脊髓小脑共济失调3型3家系患者的临床表现及相关基因突变的研究
6.
Clinical Phenotype and Genotype Characteristics of SCA 1,2,3 in Han Nationality of Henan Province
河南汉族人群脊髓小脑共济失调1、2、3 型患者临床表型特征及基因分型的研究
7.
acute cerebellar ataxia
急性小脑性共济失调
8.
spinocebellar ataxia
脊髓小脑性共济失调
9.
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
10.
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
11.
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
12.
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
13.
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
14.
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
15.
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
16.
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
17.
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
18.
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