小脑性共济失调,Cerebellar ataxia英语短句,例句大全

小脑性共济失调,Cerebellar ataxia
1)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。

英文短句/例句

1.acute cerebellar ataxia急性小脑性共济失调
2.spinocebellar ataxia脊髓小脑性共济失调
3.Systematic Review of Spinocerebellar Ataxias and Clinical Study of Spinocerebellar Ataxias in the Three Gorge Reservoir Area脊髓小脑性共济失调系统评价和三峡库区脊髓小脑性共济失调临床研究
4.Clinical experiences on acupuncture for treatment of cerebellar ataxia after stroke针灸治疗中风后小脑性共济失调的临床体会
5.The Molecular Mechanism of Hereditary Cerebellar Ataxia in Waddles Mouse;Waddles小鼠遗传性小脑性共济失调的分子机制的研究
6.The Clinical Features and Molecular Biology Studies on Hereditary Spinocerebellar Ataxia Type 3 in Ningxia Area宁夏地区遗传性脊髓小脑性共济失调3型的临床与分子研究
7.Minimum prevalence of spinocerebellar ataxia 17 in the north east of England英格兰东北部17型脊髓小脑性共济失调的最低患病率
8.The Study of Genetic Diagnosis and Mitochondrial DNA Partly Mutations in Spinocerebellar Ataxia Type 3;脊髓小脑性共济失调3型的基因诊断与线粒体DNA部分突变的研究
9.Analysis and Application of Spinocerebellar Ataxia Type 1、2(SCA1、SCA 2) Gene and Mitochondrial DNA Partly Mutations in SCA1、SCA 2;脊髓小脑性共济失调1、2型基因检测分析与线粒体DNA突变的研究
10.Mutational Analysis of Glutamate Receptor Delta 2 Gene (GluR δ2) in Patients with Cerebellar Ataxia小脑性共济失调症患者谷氨酸受体δ2基因突变研究
11.Gene Diagnosis and CAG Repeat Analysis of Spinocerebellar Ataxia Cases of Guangxi Region脊髓小脑性共济失调病人的基因诊断和CAG重复扩增研究
12.Mutational Study of Exon 12 of Glutamate Receptor δ2 Gene in Patients with Cerebellar Ataxia小脑性共济失调症患者谷氨酸受体δ2基因12号外显子突变研究
13.Molecular Genetic Diagnosis and Clinical Analysis of Characteristics of Spinocerebellar Ataxia Type 2脊髓小脑性共济失调2型的分子遗传学诊断及临床分析
14.Analysis and Application of Spinocerebellar Ataxia Type 1、2、3 Gene and Mitochondrial DNA Partly Mutations in SCA1、SCA2、SCA3脊髓小脑性共济失调1、2、3型基因检测分析与线粒体DNA突变的研究
15.The Research of Clinical Features and Gene Mutation of Five Families with Spinocerebellar Ataxia in Shangdong山东地区脊髓小脑性共济失调5个家系的临床表现和基因突变分析
16.Cerebellar ataxia model and pathology in rats大鼠小脑共济失调模型及病理学研究
17.Hereditary Cerebellar Ataxia Treated by Ganoderma capsense(Lloyd)Teng,A Report of 4 Cases薄树芝制剂治疗遗传性小脑共济失调——附4例报告
18.Population based study of late onset cerebellar ataxia in south east Wales威尔士东南部地区一项关于迟发型小脑共济失调的人群调查研究

相关短句/例句

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
3)Spinocercbellar ataxias (SCAs)脊髓小脑性共济失调(SCAs)
4)hereditary cerebellar ataxia遗传性小脑共济失调
5)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。
6)cerebral ataxia脑性共济失调