目的探讨针刺疗法治疗共济失调型脑瘫的疗效。
ObjectiveTo investigate the efficacy of acupuncture in ataxia children with cerebral palsy.
方法将40例共济失调型脑瘫患者分为观察组和对照组。
Methods40 patients were divided into 2 groups, treatment group and control group.
目的探讨感觉性共济失调型CIDP的临床特点和发病机理。
Objective To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS.
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。
Objective to study the role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3).
目的研究遗传性脊髓小脑性共济失调7型（SCA7）的基因突变和临床特征。
Objective To study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (SCA7).
目的分析泛素依赖的蛋白水解通路(UPP)在转染了脊髓小脑性共济失调3型(SCA3)基因的PC 12细胞中的定位及作用。
Objective To analyze the role and location of ubiquitin-dependent proteolysis pathway (UPP) in PC12 cells transfected by plasmids with spinocerebellar ataxia type 3 (SCA3) gene.
结论通过这次研究，发现SCA1、SCA2、SCA3型在不明原因的共济失调中的发生率为22.8%，其中又以SCA3型为主，确定诊断的最直接最有效的手段是基因诊断。
Conclusion the incidence of SCA1, SCA2 and SCA3 is 22.8% in patients with ataxia of unknown origin, and SCA3 is main type. Genetic analysis is the most effective means for the diagnosis of SCA.
结论通过这次研究，发现SCA1、SCA2、SCA3型在不明原因的共济失调中的发生率为22.8%，其中又以SCA3型为主，确定诊断的最直接最有效的手段是基因诊断。
Conclusion the incidence of SCA1, SCA2 and SCA3 is 22.8% in patients with ataxia of unknown origin, and SCA3 is main type. Genetic analysis is the most effective means for the diagnosis of SCA.
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