mitochondrial myopathy

A case of mitochondrial myopathy

线粒体肌病1例

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

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）

Objective To study the mitochondrial DNA deletion of mitochondrial myopathy and mitochondrial encephalomyopathy.

目的为了检测线粒体肌病和脑肌病患者的骨骼肌细胞的线粒体DNA的缺失情况。

Congenital hypertrophic cardiomyopathy, cataract, mitochondrial myopathy and defec-tive oxidative phosphorylation in two sib-lings with Sengers-like syndrome

在2例患有新格斯样综合征的同胞兄弟身上的先天性肥大心肌症、白内障、线粒性肌病和氧化磷酸化反应缺陷

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

A study on ultrastructural changes of mitochondrial myopathy

线粒体肌病超微结构特征研究

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

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。

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

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

An ultrastructural study on mitochondrial myopathy

线粒体肌病的电镜图像分析研究

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

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

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

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。

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

Objective: To inquire into the pathological significance of ultrastructural changes and the possible cause and pathogenesis in patients with mitochondrial myopathy.

目的：结合线粒体肌病超微结构变化的特征，探讨该病的病因和可能的发病机制。

We thought that the "white-body" disease should be one of mitochondrial myopathy, was lipid storage myopathy.

分析该病可能是一种线粒体肌病，属脂质沉积性肌病。

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。

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。