15 cases of mitochondrial disease identified by muscle biopsies and 15 normal subjects were studied.

1、

Diagnosis value of minimum exercise test of lactic acid and pyruvic acid for mitochondrial myopathy

乳酸和丙酮酸最小运动量试验对线粒体肌病的诊断价值

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2、

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

线粒体肌病与其它神经肌病破碎红纤维的对比研究

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3、

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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4、

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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5、

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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6、

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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7、

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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8、

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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9、

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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10、

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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11、

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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12、

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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13、

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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14、

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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15、

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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16、

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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17、

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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18、

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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19、

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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20、

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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