Aberrance analysis of mitochondrial DNA in a family with hereditary ataxia in Guangxi province;
遗传性共济失调一家系中发现的线粒体DNA突变
Study of mitochondrial DNA point mutations at positions 3243, 8993 in hereditary ataxia;
遗传性共济失调线粒体DNA3243、8993点突变的研究
Objective:To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia.
目的:探索线粒体DNA点突变与遗传性共济失调的关系。
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
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
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
acute cerebellar ataxia
急性小脑性共济失调
spinocebellar ataxia
脊髓小脑性共济失调
Mitochondrial DNA Point Mutations Studies in Hereditary Ataxia;
遗传性共济失调线粒体DNA部分点突变的研究
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
Molecular Diagnostic Methods for Wilson Disease, Huntington Disease and Spinocerebellar Ataxia
肝豆状核变性、亨廷顿病和遗传性共济失调的分子诊断方法研究
Cerebellar ataxia model and pathology in rats
大鼠小脑共济失调模型及病理学研究
It is the most frequent of the hereditaryAtaxias and it affects approximately1 person out of30'000.
这是最常见的遗传性共济失调，大约每30，000人中会有1人患有此病。
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
