1)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
英文短句/例句
1.spinocebellar ataxia脊髓小脑性共济失调
2.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
3.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
4.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
5.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
6.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
7.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
8.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
9.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
10.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
11.Experimental Study of Neural Stem Cells/Progenitors Transplantation on Spinocerebellar Ataxian Rat;神经干/祖细胞移植治疗脊髓小脑共济失调大鼠的实验研究
12.acute cerebellar ataxia急性小脑性共济失调
13.Research of Clinical Features and Gene Mutation of Patients with Spinocerebellar Ataxia Type 3 in Three Families;脊髓小脑共济失调3型3家系患者的临床表现及相关基因突变的研究
14.Clinical Phenotype and Genotype Characteristics of SCA 1,2,3 in Han Nationality of Henan Province河南汉族人群脊髓小脑共济失调1、2、3 型患者临床表型特征及基因分型的研究
15.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
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.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
18.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
相关短句/例句
Spinocercbellar ataxias (SCAs)脊髓小脑性共济失调(SCAs)
3)spinocerebellar ataxia脊髓小脑共济失调
4)spinocerebellar ataxia type 1脊髓小脑共济失调1型
1.Clinical analysis on the cases with intermediate Cytosine-Adenine-Guanine repeat alleles of spinocerebellar ataxia type 1;脊髓小脑共济失调1型中等重复动态突变患者临床表型分析
5)spinocerebellar ataxia type2脊髓小脑共济失调2型
1.Clinical characteristics and MRI features of 8 spinocerebellar ataxia type2 and type3 patients;8例脊髓小脑共济失调2型、3型患者的临床表型及MRI表现分析
6)Spinocerebellar ataxias脊髓小脑共济失调
延伸阅读
脊髓性共济失调脊髓性共济失调spinal ataxia 又称Friedreich共济失调。脊髓小脑束和后索变性所致的随意运动不协调。此外，脊柱中的神经细胞和后根纤维的退行性、继发性萎缩也可引起本病。本病为常染色体隐性遗传，发病多始于幼年或少年，随年龄的增长而加重。其表现为行走缓慢、两腿叉开、左右摇摆、蹒跚如醉，跟膝胫试验阳性，两下肢深部感觉及膝腱、跟腱反射减弱或消失。两侧babinski征阳性。常造成严重的脊柱侧凸或后凸及弓形足。晚期有程度不同的瘫痪和膀胱、直肠功能障碍。
