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。
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
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
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。
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
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
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
heredopathia atactic polyneuritifor
多神经炎型遗传性运动失调
lacking motor coordination; marked or caused by ataxia.
缺乏运动协调；有明显的运动失调特点或由运动性共济失调引起。
Gini-index genetic algorithm for the scheduling problems with similar characteristics
基尼指数遗传算法求解具有共性的调度问题
Friedreich's ataxia
弗里德赖希氏共济失调
Friedrich's ataxia
弗里德利希共济失调
Research of Chaos Genetic Algorithm on AGC Units Deployment;
AGC机组调配经济性的混沌遗传算法研究
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
Sensory Ataxia Form of Chronic Inflammatory Demyelinating Polyneuropathy
感觉性共济失调型慢性炎性脱髓鞘性多发性神经病