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1)  cerebral ataxia
脑性共济失调
2)  Cerebellar ataxia
小脑性共济失调
1.
Consciousness disorders and cerebellar ataxia in one patient induced by large dose oral administration of carbamaze-pine;
大剂量服用卡马西平出现意识障碍、小脑性共济失调1例
2.
The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed.
回顾小脑性共济失调的研究历史、分类,介绍脊髓小脑共济失调的病因机制和治疗方法。
3.
GluRδ2 deficiency or mutations cause ataxia which is very similar to cerebellar ataxias.
背景:小脑性共济失调是一组具有高度临床和遗传异质性的神经系统退行性疾病。
3)  Spinocerebellar ataxia
脊髓小脑性共济失调
1.
Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias;
脊髓小脑性共济失调的分子遗传学诊断与临床应用
2.
Molecular genetic diagnosis and clinical characteristics of spinocerebellar ataxia type 6;
脊髓小脑性共济失调6型的分子遗传学诊断及临床特点
3.
Molecular genetic diagnosis and clinical analysis of spinocerebellar ataxia type7;
脊髓小脑性共济失调7型的分子遗传学诊断及临床分析
4)  Spinocercbellar ataxias (SCAs)
脊髓小脑性共济失调(SCAs)
5)  hereditary cerebellar ataxia
遗传性小脑共济失调
6)  cerebellar ataxia
小脑共济失调
1.
Objective To establish an animal model of cerebellar ataxia by injecting kainic acid(KA) into SD rat\'s bilateral cerebellar fastigial nuclei and to observe the praxiological and pathological change of SD rat\'s ataxia.
目的建立SD大鼠海人酸(KA)损毁双侧小脑顶核制备的小脑共济失调动物模型;观察其共济失调的行为学和病理学改变。
补充资料:脑性
1.指意识。
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