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- A story of a brave man who despite his spinocerebellar ataxia refuses to give up volunteering. 一個(gè)罹患小腦萎縮癥患者、不因生病放棄做志工的故事。
- Objective To study the gene mutation and clinical characteristics of hereditary spinocerebellar ataxia type 7 (SCA7). 摘要目的研究中國人遺傳性脊髓小腦型共濟失調(SCA)7型(SCA7)的基因突變和臨床特征。
- We report two brothers with a progressive cerebellar syndrome due to spinocerebellar ataxia type 8 (SCA8). 我們報告了兩個(gè)患有漸進(jìn)性小腦綜合征的兄弟，是由于8型脊髓小腦共濟失調(SCA8)所致。
- Objective To explore the clinical and molecular biological characteristics of spinocerebellar ataxia type 3 (SCA3). 摘要目的探討脊髓小腦性共濟失調(SCA)3型的臨床與分子生物學(xué)特征。
- Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia. 目的探討遺傳性脊髓小腦型共濟失調(SCA)病人SCA3基因突變的意義。
- Methods:Fragment analysis based on CEQ8000 sequencer were applied to analyze the CAG repeat of SCA1 gene in two autosomal dominant inherited spinocerebellar ataxia pedigrees. 方法:采用基于CEQ8000核酸分析儀的片段分析方法對2個(gè)表型為常染色體顯性遺傳脊髓小腦共濟失調家系進(jìn)行SCA1基因CAG重復序列突變檢測,并分析其臨床特征。
- Tzu Chi volunteer Cai Caizhong from Kaohsiung contracted spinocerebellar ataxia two years ago.The disease gradually destroys his ability to move and talk. 住在高雄的慈濟志工蔡財忠兩年前被發(fā)現罹患小腦萎縮癥，語(yǔ)言能力以及行動(dòng)開(kāi)始退化；
- Objective:To investigate the clinical features of the cases with intermediate Cytosine-Adenine-Guanine(CAG) repeat alleles of spinocerebellar ataxia type 1(SCA1). 目的:探討脊髓小腦共濟失調1型(SCA1)中等重復動(dòng)態(tài)突變患者臨床表型特征。
- The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed. The pathogenesis and treatments of spinocerebellar ataxia were summarizd. 回顧小腦性共濟失調的研究歷史、分類(lèi),介紹脊髓小腦共濟失調的病因機制和治療方法。
- Objective To construct spinocerebellar ataxia 3 (SCA3) eukarotic expression vector with enhanced green fluorescent protein (EGFP) as report gene and to observe its expression in PC12 cells. 目的構建以增強型綠色熒光蛋白(EGFP)作為報告基因、帶有脊髓小腦性共濟失調3型(SCA3)基因的真核細胞表達載體,并轉染PC12細胞,觀(guān)察外源基因的表達情況。
- Abstract: The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed.The pathogenesis and treatments of spinocerebellar ataxia were summarizd. 摘 要: 回顧小腦性共濟失調的研究歷史、分類(lèi)，介紹脊髓小腦共濟失調的病因機制和治療方法。
- hereditary spinocerebellar ataxia 遺傳性脊髓小腦性共濟失調
- spinocerebellar Ataxia(SCA) 脊髓小腦共濟失調（SCA）
- Minimum prevalence of spinocerebellar ataxia 17 in the north east of England 英格蘭東北部17型脊髓小腦性共濟失調的最低患病率
- A DETECTION OF SCA_3 MUTATION IN PATIENTS WITH INHERITED SPINOCEREBELLAR ATAXIA 遺傳性脊髓小腦型共濟失調病人SCA_3基因突變檢測
- Keywords spinocerebellar ataxia 7;trinucleotide repeat;mutation detection; 脊髓小腦性共濟失調7型;三核苷酸重復;突變檢測;
- Keywords hereditary spinocerebellar ataxia;trinucleotide repeat;gene diagnosis; 遺傳性脊髓小腦型共濟失調;三核苷酸重復;基因診斷;
- Keywords Spinocerebellar ataxia Gene Trinucleotide repeat Dynamic mutation; 脊髓小腦型共濟失調;基因;三核苷酸重復;動(dòng)態(tài)突變;
- An SCA module is not just another type of package. SCA模塊并非只是另一種類(lèi)型的包。
- First, we will define the SCA component. 首先,我們要定義SCA組件。
