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Spinocerebellar的意思
1、脊髓小脑径
Spinocerebellar的相关词组
1、Spinocerebellar ataxias 脊髓小脑共济失调；脊髓小脑共济失调症
2、Spinocerebellar ataxia 共济失调；脊髓小脑性共济失调；小脑萎缩症
Spinocerebellar的双语例句
1、Projections from cervical spinocerebellar tract neurons to cerebellar nuclei in rats by the anterograde labeling of biotinylated dextran amine
生物素化葡聚糖胺法顺行追踪大鼠颈段脊髓小脑束神经元向小脑中央核的投射
2、CONCLUSION: The cervical segments of spinocerebellar tract project to the cerebellar nuclei in rats and locate somatotopically as compared with the lumbar spinal cord.
结论：大鼠脊髓颈段有向小脑中央核的投射，与腰髓的投射相比较，存在一定的定位关系。
3、Role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3
细胞凋亡在脊髓小脑性共济失调3型发病机制中的作用
4、To study the molecular genetic diagnosis and clinical characteristics of spinocerebellar ataxia type 12 ( SCA12).
【目的】研究分析脊髓小脑性共济失调12型（SCA12）的分子诊断及临床表现特征。
5、Objective To study the role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3 ( SCA3).
目的研究细胞凋亡在脊髓小脑性共济失调3型（SCA3）分子发病机制中的作用。
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、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
8、Analysis of the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7
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
9、A study on presymptomatic testing for spinocerebellar ataxias
脊髓小脑性共济失调的症状前诊断研究
10、Establishment of germplasm repository of spinocerebellar ataxia
脊髓小脑性共济失调遗传种质库的建立
11、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
12、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
13、Spinocerebellar ataxias is a global disease which were reported in 6 continents including 39 countries or areas.
结论：1.脊髓小脑性共济失调是一个世界范围的神经系统遗传疾病，遍布全球6大洲39个国家地区。
14、We diagnosised 1 sporadic patients of spinocerebellar ataxia type 3 for the first time in the Three Gorge Reservoir Area. 4.
三峡库区首次确诊1名脊髓小脑性共济失调3型散发患者。
15、We diagnosised 2 spinocerebellar ataxia type 3 pedigrees, including 20 familial patients, for the first time in the Three Gorge Reservoir Area. 3.
三峡库区首次确诊2个脊髓小脑性共济失调3型家系，其中有20名家系患者。
16、Families with 25 patients and 6 sporadic cases involed in spinocerebellar ataxias;
临床上被诊断为脊髓小脑共济失调的具有家族遗传史的8个家系25名患者，无家族史的散发病例6个患者。
17、Objective: Spinocerebellar ataxias, which is a hereditary neurological degenerative disorders, are incurable at present.
目的：脊髓小脑共济失调是一种遗传性神经系统变性疾病，目前仍无理想治疗方法。
18、Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6
中国大陆汉族人群SCA各亚型的突变频率分析及SCA6的临床和分子特征
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