A comparative study of ragged red fibers between mitochondrial myopathy and other neuromuscular disorders

1、

Electron microscopy findings in a series of 16 cases of mitochondrial myopathy and encephalomyopathy

16例线粒体肌病和线粒体脑肌病电镜观察分析

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2、

A study on ultrastructural changes of mitochondrial myopathy

线粒体肌病超微结构特征研究

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Reactive oxygen species Aerobic exercise and muscle metabolism in patients with mitochondrial myopathy

线粒体肌病患者的有氧训练与肌肉新陈代谢

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4、

Clinical and pathological characteristics of pure type mitochondrial myopathy

单纯型线粒体肌病的临床和病理特点

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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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6、

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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7、

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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8、

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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9、

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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10、

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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11、

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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12、

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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13、

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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14、

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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15、

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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16、

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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17、

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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18、

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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19、

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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20、

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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