1) Cerebellar Ataxia/acup-mox ther
小脑性共济失调/针灸疗法
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)
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：小脑性共济失调性腺功能减退综合征
小脑性共济失调性腺功能减退综合征
病名。由于神经与内分泌疾病属遗传性、偶然凑合，或垂体功能不足，原发性发育不全或继发于不能分泌促性腺激素所致。并非代表一组性质相同的疾病。疾因不明。临床可见小脑综合征(Marie共济失调，Friedreich共济失调或新小脑综合征)和原发性性腺功能减退症合并出现。在青春期中，垂体完全或部分不能刺激性腺发育。尿中促性腺激素减少。性腺功能减退者，可用激素治疗。预后取决于小脑综合征的严重程度。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条