脊髓小脑
- 名spinocerebellum
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癫痫主要影响小脑前叶,即脊髓小脑区域,这可能与该部位特殊的生理功能和解剖联系有关。
Epilepsy mainly affects anterior lobe of cerebellum , namely spinocerebellum , which may be due to the special physiological function and anatomical structure of the lobe .
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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 clinical features and genetic mutation frequency of spinocerebellar ataxia ( SCA ) type 6 from Chinese kindreds .
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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 .
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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。
The present study examined whether the lumbar spinocerebellar tract projects to the cerebellar nuclei , by using anterograde labeling with biotinylated dextran ( BDA ) .
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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。
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 .
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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。
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 .
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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。
Families with 25 patients and 6 sporadic cases involed in spinocerebellar ataxias ;
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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
Analysis of the clinical features and genetic mutation of spinocerebellar ataxia type 6 from Chinese kindreds
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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
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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。
Objective : Spinocerebellar ataxias , which is a hereditary neurological degenerative disorders , are incurable at present .
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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
Projections from cervical spinocerebellar tract neurons to cerebellar nuclei in rats by the anterograde labeling of biotinylated dextran amine
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三核苷酸重复的检测在脊髓小脑型共济失调的应用研究
Detection of trinucleotide repeat expansions in the study of hereditary spinocerebellar ataxia ( SCA ) and its clinical significance
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本研究采用10只家兔进行腰、骶、尾髓的脊髓小脑束乙酰胆碱酯酶阳性神经元定位研究。
10 rabbits were used in the present study for localization of the cholinergic neurons of the spinocerebellar tracts in the lumbo-sacro-coccygeal cord .
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大鼠脊髓小脑前束起始细胞&脊髓边缘细胞突触形态学的电镜研究
The synaptology of the spinal border cells & the original neurons of ventral spinocerebellar tract in the rat : an electron microscopic study
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用麦芽凝集素结合辣根过氧化酶和溃变法顺行追踪猫骶尾髓脊髓小脑神经元的投射
The Projection of Spinocerebellar Neurons from the Sacrococcygeal Spinal Cord in the Cat . An Experimental Study Using Anterograde Transport of WGA-HRP and Degeneration
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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。
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 .
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目的:检测Nogo-A蛋白在纯化后的大鼠脊髓和小脑细胞核中的表达。
Objective : To investigate the expression of Nogo-A in relatively purified nucleus fractions from rat spinal cord and cerebellum .
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双标免疫荧光检测法显示RIM3γ分布在大鼠的大脑皮层、脊髓和小脑的某些抑制性神经元。
Double labeled fluorescence assay showed the expression of RIM3 γ in some inhibitory neurons of the cortex , the spinal cord and the cerebellum of adult Wistar rats .
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目的研究脊髓腹侧及小脑病变是否可致胫神经刺激C2、枕点诱发电位出现异常改变以及正中神经、胫神经刺激,两者C2、枕部诱发电位的差异。
Objective To study whether the lesions on cerebellum and spinal cord ventrally could affect the evoked potential recorded on C2 and occiput , and check the difference between the evoked potentials from stimulating median and tibial nerve .
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其在脊髓、脑和小脑中的分布较少,表明来乐司酮对中枢神经系统影响不大;
The absorption in spinal cord , brain and cerebellum is very little .
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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
Electron microscopic study on synaptic connections of rubrospinal tract to original cells of spinocerebellar tract in rats
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实验提示红核脊髓束与脊髓小脑束起始细胞存在直接或间接的突触联系。
The findings suggested that RST terminations might have synaptic contact with the original cells directly or indirectly .
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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。
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 .
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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
Synaptic relationship between the terminals of vestibulospinal tracts and the original cells of spinocerebellar tracts in the rat
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将12只成年大鼠一侧脊髓段灰质行电损毁后用溃变法追踪脊髓小脑吻侧束纤维在脊髓、脑干内的走行及在小脑内的分布。
Degeneration was made in12 adult rats to study the course and projections of the rostral spinocerebellar tract ( RSCT ), after unilateral lesions in the C_ ( 5 ~ 8 ) spinal segments .