遗传性共济失调

遗传性共济失调的头部MR影像1例

Note that Mr. Brain MRI of hereditary ataxia disease : case report

线粒体DNA部分点突变与遗传性共济失调的关系研究

Mitochondrial DNA point mutations studies in hereditary ataxia

前言：目的：探索线粒体DNA点突变与遗传性共济失调的关系。

Objective : To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia .

目的探索遗传性共济失调（hereditaryataxia，HA）家系中的线粒体DNA突变。

Objective To investigate the point mutations of mitochondrial DNA in the families with hereditary ataxia .

目的探索线粒体DNA部分点突变与遗传性共济失调（hereditaryataxia，HA）的关系。

Objective To study the possible relationship between mitochondrial DNA ( mtDNA ) and hereditary ataxia ( HA ) .

目的：对新疆地区两个遗传性共济失调（SCAs）家系进行基因突变分析，研究该类疾病的临床表现与基因突变的特点。

Objective : To investigate the clinical manifestation and the gene mutation characteristics of two SCAs families from Xinjiang .

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

Molecular Diagnostic Methods for Wilson Disease , Huntington Disease and Spinocerebellar Ataxia

通过细胞周期检查排除/确认遗传性共济失调-毛细血管扩张患儿

Exclusion / confirmation of Ataxia-telangiectasia via cell-cycle testing

国内南方人群遗传性共济失调不同基因亚型的分布状况（英文）积累与分配的关系；

Distribution of different genotypes of hereditary ataxia in south China Accumulation and distribution ;

遗传性小脑共济失调的MRI表现附2个家系报告

MRI Findings of Hereditary Cerebellar Ataxia

遗传性小脑共济失调的多形式诱发电位研究

A study on multimodal evoked potentials in the patients with hereditary cerebellar ataxias

Waddles小鼠遗传性小脑性共济失调的分子机制的研究

The Molecular Mechanism of Hereditary Cerebellar Ataxia in Waddles Mouse

犊牛遗传性小脑萎缩共济失调研究报告

Study on heredo - cerebellar - atrophy - ataxia in calf

遗传性痉挛性共济失调&附1家族4代9例报告

Hereditary spastic ataxia & a report of 9 cases of 4 generations in one family

1目的探讨遗传性脊髓小脑型共济失调（SCA）病人SCA3基因突变的意义。

Objective To explore SCA 3 gene mutation in the patients with inherited spinocerebellar ataxia .

遗传性脊髓小脑性共济失调7型的基因突变及临床特征分析

Analysis of the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7

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

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

湖南汉族人群遗传性脊髓小脑型共济失调患者三核苷酸突变频率分布

Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China