脊髓小脑的

基本解释 (translations)

spinicerebellar  ·  spinocerebellar

与脊髓小脑的相关的网络例句 [注：此内容来源于网络，仅供参考]

Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia.

目的 探讨遗传性脊髓小脑型共济失调病人SCA3基因突变的意义。

Objective To study the gene mutation of the spinocerebellar ataxia（SCA types 1～3 in the patients with primary dystonia.

目的 研究原发性肌张力障碍患者脊髓小脑性共济失调1～3型基因的突变。

These DSs were first observed at 9 weeks in the distal part of ascending fibers that consist of gracile fasciculus and cerebellospinal-gracile nucleus and white matter of cerebellum. They extend along medulla oblongate to medulla cervix、medulla thorax、medulla lumbalis in accordance with dying-back type degeneration. The corticospinal tract were affected at 18 weeks,and thalamus、the olfactory pathway、the visal pathway、the auditory pathway were affected at 32 weeks.

这种DS从9周龄开始，首先在构成薄束路和脊髓小脑后路的上行纤维的远端区域-薄束核区和小脑白质出现，逐渐按照延髓、颈髓、胸髓、腰髓的顺序，向细胞体方向逆行性地进展。18周龄时波及到锥体路，32周龄时进一步波及到丘脑和嗅觉、视觉、听觉传导路。

Objective To study the gene mutation characteristics of patients with spinocerebellar ataxias in Ningxia region.

目的 研究宁夏地区脊髓小脑性共济失调患者基因突变的特征。

Objective To determine the frequency of different subtypes of spinocerebellar ataxias in the Han nationality of Hunan province in China.

目的：研究湖南汉族人群中脊髓小脑性共济失调不同基因亚型的分布状况。

Spinocerebellar ataxias are a group of autosomal dominant cerebellar degenerative disorders, which are characterized by clinical and genetic variability.

脊髓小脑性共济失调是一组常染色体显性的小脑退行性病，具有临床和遗传多样性。

We investigated the clinical features and gene mutation in a pedigree of spinocerebellar ataxia.

对一脊髓小脑性共济失调(Spinocerebenllar ataxia， SCA)家系的患者进行临床特征及相关基因突变研究。

Spinocerebellar ataxia type 7 (SCA7) is less variable in clinical presentation than other SCAs.

脊髓小脑性共济失调7型（SCA7）的临床表现形式较其它SCA类型少。

Objective To investigate the related factors of International Cooperative Ataxia Rating Scale score on spinocerebellar ataxia type 3 (SCA3) patients.

目的探讨国际协作共济失调评估量表评估脊髓小脑共济失调3型患者的相关因素。

Conversely, injury to the reticulospinal or vestibulospinal tracts, which normally inhibit spinal reflex pathways, results in "positive" symptoms including spasticity, hyperactive muscle stretch reflexes, abnormal cutaneous and autonomic reflexes, and co-contraction of agonist and antagonist muscles.

相反，一般不影响脊髓反射通路的皮质脊髓束和小脑脊髓束的损伤导致阳性效应，包括痉挛、牵张反射亢进、病理的皮肤反射和自主反射、相互拮抗肌的共同紧张。

与脊髓小脑的相关的网络解释 [注：此内容来源于网络，仅供参考]

SCA：脊髓小脑共济失调

自Menzel(1891)首先发现常染色体显性遗传性脊髓小脑共济失调(SCA)以来,近百余年时间,相继在世界各地均有报道,大部分病例的病理改变主要在小脑、脑干、脊髓、基底节和大脑皮质等处,表现为神经轴索变性、髓鞘脱失、神经元脱失等.

cerebellopontile：小脑脑桥的

cerebellofugal 小脑传出的 | cerebellopontile 小脑脑桥的 | cerebellospinal 小脑脊髓的

cerebellorubral：小脑红核的

cerebellopontineangle 桥小脑角 | cerebellorubral 小脑红核的 | cerebellorubrospinal 小脑红核脊髓的

cerebellospinal：小脑脊髓的

cerebellopontile 小脑脑桥的 | cerebellospinal 小脑脊髓的 | cerebellospinal tract 小脑脊髓径

cerebellospinal tract：小脑脊髓径

cerebellospinal 小脑脊髓的 | cerebellospinal tract 小脑脊髓径 | cerebellum 小脑

spinobulbar tract：脊髓延髓径

spinobulbar 脊髓延髓的 | spinobulbar tract 脊髓延髓径 | spinocerebellar 脊髓小脑的

spinocerebellar：脊髓小脑的

spinobulbar tract 脊髓延髓径 | spinocerebellar 脊髓小脑的 | spinocerebellar tract 脊髓小脑径

spinocerebellar tract：脊髓小脑径

spinocerebellar 脊髓小脑的 | spinocerebellar tract 脊髓小脑径 | spinocortical 脊髓大脑皮层的

Spinocerebellar ataxia：脊髓小脑性共济失调

在这项新的研究中,为了弄清miRNA途径是否在神经退化过程中起到一定的作用,研究人员分析了对miRNA加工过程很关键的基因如何调节由III型脊髓小脑性共济失调(spinocerebellar ataxia)蛋白诱导的毒性.

posterior spinocerebellar tract：脊髓小脑后束

不产生意识感觉, 而是反射性调节躯干和四肢的肌张力和协调运动, 以维持身体的姿势和平衡.⑴ 脊髓小脑后束(Posterior spinocerebellar tract) ⑵ 脊髓小脑前束(Anterior spinocerebellar tract) 躯干四肢非意识性 本体觉, 本体觉,