Clinical and pathological characteristics of pure type mitochondrial myopathy

1、

Primary mitochondrial myopathy and encephalo myopathy ( A report of 53 cases)

原发性线粒体肌病与脑肌病（附53例报告）

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2、

Study in mitochondrial gene defect of patients with mitochondrial myopathy and encephalomyopathy

线粒体肌病和脑肌病患者线粒体基因缺失的研究

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3、

Study on histochemistry and ultrastructure of mitochondrial myopathy and mitochondrial encephalomyopathy

线粒体肌病和线粒体脑肌病组织化学及电镜的研究

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4、

Changes of enzyme histochemistry and ultrastructure in mitochondrial myopathy and encephalomyopathy

线粒体肌病与线粒体脑肌病的酶组织化学和超微结构改变

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5、

Methods Clinical manifestations, family histories and pathological findings of 21 patients with CPEO type of mitochondrial myopathy from 3 families constellations were analyzed retrospectively.

方法回顾性分析CPEO型线粒体肌病3个家系21例患者的临床表现、家系调查及5例肌活检病理学资料。

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6、

Objective To investigate the clinical, genetic and pathological features of familial chronic progressive external ophthalmoplegia ( CPEO) type of mitochondrial myopathy.

目的探讨家族性慢性进行性眼外肌瘫痪（CPEO）型线粒体肌病的临床、遗传和病理特点。

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7、

Objective To establish and evaluate denaturing high-performance liquid chromatography ( DHPLC) as a rapid and efficient technique of detecting mutations of mitochondrion gene.

目的以变性高效液相色谱（DHPLC）技术分析检测线粒体肌病患者线粒体基因突变，以明确诊断。

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8、

Conclusion The mtDNA deletion is considered to be an important cause of mitochondrial diseases.

结论mtDNA基因缺失是线粒体肌病和脑肌病的重要病因之一。

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9、

Quantitative analysis of mitochondrial DNA in peripheral blood cells of patients with mitochondrial myopathy/ encephalomyopathy

线粒体肌病和脑肌病外周血细胞线粒体DNA的定量分析

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10、

Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy

线粒体肌病患者线粒体DNA的突变分析

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11、

In pure mitochondrial myopathy and CPEO group, none had the 5 point mutations.

单纯型线粒体肌病组和CPEO组均未发现以上5个位点的突变。

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12、

Methods By using total mtDNA abstracted from skeletal muscles in the patient with mitochondrial myopathy and encephalomyopathy.

方法从1例线粒体肌病和1例脑肌病（MERRF）患者骨骼肌活检标本中，提取总DNA，以限制性内切酶PvuⅡ酶切，与mtDNA全长探针进行分子杂交。

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13、

Generally, they can be classified into three different subgroups: polymyositis, dermatomyositis and inclusion body myositis.

一般来说，它们可分为三个不同的亚组：多发性肌炎，皮肌炎和包涵体肌炎。

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14、

Objective To further discuss the diagnostic criteria for characterize of inclusion body myositis ( IBM).

目的探讨包涵体肌炎的诊断标准。

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15、

Pathological and immunopathological changes of polymyositis and inclusion body myositis

多发性肌炎及包涵体肌炎的病理和免疫病理变化

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16、

Inclusion Body Myositis: A Case Report and Literature Review

包涵体肌炎1例报告并文献复习

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17、

Epidemiological Investigation on Spotted Fever Group Rickettsiae and Coinfection with Borrelia Burgdorferi Sensu Lato in Several Provinces, China

我国部分省区蜱传斑点热及其与莱姆病复合感染的流行病学调查研究

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18、

Lyme disease is a newly discovered tick-borne disease caused by Borrelia burgdorferi sensu lato.

莱姆病是一种新发现的蜱传自然疫源性疾病，其病原体为伯氏疏螺旋体（Borrelia burgdorferi sensu lato）。

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19、

Genotyping of Borrelia burgdorferi sensu lato isolated from Northeastern Forest Areas of China

我国东北林区蜱中伯氏疏螺旋体的分离及分型鉴定

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20、

Study on the coinfection status of Borrelia burgdorferi sensu lato and spotted fever group Rickettsia in ticks from Hunchun, Jilin province

吉林省珲春地区蜱中伯氏疏螺旋体与斑点热群立克次体复合感染研究

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