myopathy

Cytoplasmic body myopathy masquerading as motor neuron disease

胞浆体肌病误认为运动神经元病

In these patients, steroid-induced myopathy may lead to additional morbidity.

在这些患者中, 类固醇诱导肌病有更高的发病率.

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

Skeletal muscle was the main target tissue of diabetic damages. The diabetic myopathy aggravated insulin resistance.

骨骼肌是全身利用葡萄糖最重要的组织之一，也是高血糖损害的主要靶位，骨骼肌病变又使外周胰岛素抵抗加重。

Electromyographic Study in Patients with Thyrotoxic Myopathy

甲状腺功能亢进性肌病肌电图的研究

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。

Steroid myopathy may be reversible with a reduction of dose or discontinuation of the steroid.

停用类固醇或减量后,类固醇肌病是可逆的.

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

Purpose: To report clinical and pathological characterisitics of 3 cases with mitochondrial encephalo-myopathy ( MELAS type) including 2 cases from one family and 1 sporadic case.

报告3例线粒体脑肌病MELAS型患者的临床资料及病理特点。其中2例为一家系兄妹2人，另1例为散发。

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

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

Objective To study the clinic and pathological features of 4 cases of lipid storage myopathy ( LSM) and differential diagnosis with Duchenne/ Becker muscular dystrophy 、 limb-girdle muscular dystrophies and polymyositis.

目的通过分析4例被误诊的脂质沉积性肌病的临床及病理特点，探讨脂质沉积性肌病被误诊的原因及与假肥大型肌营养不良、肢带型肌营养不良及多发性肌炎的鉴别诊断。

In this paper, 2 patients with mitochon-drial myopathy and 3 patients, with mitochon-drial encephalomyopathy ( 1 case with MELAS, 2 cases with MERRF) were reported.

本文报告了2例线粒体肌病、3例线粒体脑肌病（MALES1例、MER-RF2例）。

19 Cases of chronic thyrotoxic myopathy ( CTM) are reported.

对19例慢性甲状腺机能亢进性肌病，进行了回顾性研究。

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。

Objective To investigate the clinical manifestations and pathological features nemaline myopathy ( NM ) .

目的探讨 杆状体 肌病的临床表现和病理特点.

An ultrastructural study on mitochondrial myopathy

线粒体肌病的电镜图像分析研究

Systemic amyloidosis with myopathy as the first manifestation: a case report

以肌病为首发表现的系统性淀粉样变性一例

Myotubular myopathy ( XLMTM ) is a usually very severe congenital myopathy associated with major hypotonia at birth.

肌管性肌病 ( XLMTM ) 通常是非常严重的先天性肌病并伴随着大部分肌肉的张力过弱.

We experimentalize in order to investigate these factors whether express in alcoholic myopathy or not.

本实验旨在研究慢性酒精性肌病的发病过程中这些因子是否有表达。

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

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

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

Left atrial myopathy in cardiac amyloidosis: Implications of novel echocardiographic techniques

心脏淀粉样变性时的左心房心肌病：超声心动图新技术的意义

Chronic Thyrotoxic Myopathy-One Case Report

慢性甲状腺机能亢进性肌病1例临床和病理报告

A case of mitochondrial myopathy

线粒体肌病1例

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。

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

The Experiment of Emergency Treatment and Nursing in 4 Cases of Acute Thyrotoxic Myopathy

4例急性甲亢肌病的抢救护理体会

A study on ultrastructural changes of mitochondrial myopathy

线粒体肌病超微结构特征研究