spinocerebellar
英
美
网络 脊髓小脑径; 脊髓小脑的
双语例句
- 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 - Gene Diagnosis and CAG Repeat Analysis of Spinocerebellar Ataxia Cases of Guangxi Region Treating Four Refractory and Relapse Acute Myelocytic Leukemia Patients with Sequential Dual Induction Chemotherapy: FA Combined with Priming Chemotherapy
脊髓小脑性共济失调病人的基因诊断和CAG重复扩增研究FA+CAG序贯双诱导治疗复发难治急性髓系白血病4例 - 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 - 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 - 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 - 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 - Objectives: To study the contents of excitatory amino acids ( EAAs) and inhibitory amino acids ( IAAs) in cerebrospinal fluid ( CSF) in patients with spinocerebellar degeneration ( SCD) and the correlation between SCD and clinical features.
目的：探讨脊髓小脑变性（SCD）患者脑脊液中兴奋性和抑制性氨基酸的变化。目的：为研究脑梗死后脑内抑制性氨基酸（IAAs）递质的变化规律及其意义。 - The present study examined whether the lumbar spinocerebellar tract projects to the cerebellar nuclei, by using anterograde labeling with biotinylated dextran ( BDA).
本实验采用BDA顺行追踪法研究了大鼠腰髓脊髓小脑束向小脑中央核的投射。 - 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 - Synaptic relationship between the terminals of vestibulospinal tracts and the original cells of spinocerebellar tracts in the rat
大鼠前庭脊髓束终末与脊髓小脑束起源细胞间的突触联系 - Electron microscopic study on synaptic connections of rubrospinal tract to original cells of spinocerebellar tract in rats
大鼠红核脊髓束与脊髓小脑束起始细胞突触联系的电镜研究 - Spinocerebellar ataxias ( SCAs) are a heterogeneous group of neurological disorders characterized by variable degrees of degeneration of the cerebellum, spinocerebellar tracts, and brain stem neurons.
脊髓小脑共济失调（SCAs）是一组具有多变的小脑、脊髓小脑束和脑干神经元变性的异质性神经病。 - Establishment of germplasm repository of spinocerebellar ataxia
脊髓小脑性共济失调遗传种质库的建立 - Detection of trinucleotide repeat expansions in the study of hereditary spinocerebellar ataxia ( SCA) and its clinical significance
三核苷酸重复的检测在脊髓小脑型共济失调的应用研究 - Analysis of the clinical features and genetic mutation of spinocerebellar ataxia type 6 from Chinese kindreds
脊髓小脑型共济失调6型患者的临床特征及基因突变分析 - 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。 - 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 - 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 - Objective To explore SCA 3 gene mutation in the patients with inherited spinocerebellar ataxia.
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。 - Using HRP retrograde transport and anterograde generation of neurons, the synaptic connections between terminates of rubrospinal tract ( RST) and original cells of spinocerebellar tract ( SCT) were observed by electron microscope.
采用神经元溃变和HRP神经元逆行追踪结合的方法，电镜观察组核脊髓束终末与脊髓小脑束起始细胞的突触联系。 - Objective To study the clinical features and genetic mutation frequency of spinocerebellar ataxia ( SCA) type 6 from Chinese kindreds.
目的研究脊髓小脑型共济失调（SCA）6型的临床特征和基因突变频率。 - 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。 - 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。 - The clinical features of the spinocerebellar ataxia include ataxa, dysarthria, dysmetria et al. The gene diagnosis can be used as diagnostic criteria and the detection of repeats times of CAG can provide an effective way for the genetic and presymptomatic diagnosis.
临床特征有共济失调、构音障碍，基因诊断是一种准确的诊断方法和标准，CAG重复序列数目的检测对于基因诊断和症状前诊断是一种十分有效的方法。 - 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。 - Spinocerebellar ataxia type 3/ Machado-Joseph disease ( SCA3/ MJD) is a kind of autosomal dominant disease, which is characterized by degeneration of neurons and accumulation of aberrant protein aggregates in affected neurons.
脊髓小脑型共济失调Ⅲ型/马查多-约瑟夫病（SCA3/MJD），是一种以神经细胞变性、细胞核内蛋白聚集体形成为病理特征的常染色体显性遗传病。 - 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。 - 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。