说明:双击或选中下面任意单词,将显示该词的音标、读音、翻译等;选中中文或多个词,将显示翻译。
您的位置:首页 -> 句库 -> 脊髓小脑共济失调
1.
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
2.
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
3.
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
4.
spinocebellar ataxia
脊髓小脑性共济失调
5.
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
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
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
13.
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
14.
acute cerebellar ataxia
急性小脑性共济失调
15.
Cerebellar ataxia model and pathology in rats
大鼠小脑共济失调模型及病理学研究
16.
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
17.
locomotor ataxia [ ataxy ]
【医】运动失调病, 脊髓痨
18.
any of several congenital disorders marked by degeneration of the cerebellum and spinal cord resulting in spasticity and ataxia.
先天小脑脊髓混乱恶化。