Objective To discuss the changes of ECG and cardiac enzyme spectrum during hypokalemic periodicit paralysis.

1、

Objective To explore the curative effect of using 131I to treat Graves disease accompanies periodic paralysis.

目的探讨131I治疗Graves病合并周期性麻痹的疗效。

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2、

Familial periodic paralysis ( PP) is an autosomal dominant disorder characterized by episodic attacks of paralysis with different severity.

家族性周期性麻痹（periodic paralysis，PP）是以反复发作骨骼肌迟缓性瘫痪为特征的一组疾病。

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3、

In the present study, invasion plasmid antigen C ( IpaC), secreted by the invasion plasmid of Shigella spp and enteroinvasive Escherichia coli, is the primary effector protein for Shigella invasion of epithelial cells.

目前的研究认为，IpaC是志贺菌属和侵袭性大肠杆菌（enteroinvasive Escherichia coli.EIEC）中侵袭性大质粒分泌的一种侵袭性蛋白，是细菌侵入肠上皮细胞所必需的。

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4、

STUDY ON PLASMID PRINTING OF SHIGELLA SPP Advance in molecular biology of Shiga toxin from Shigella dysenteriae type ⅰ

志贺菌的质粒图谱分析志贺毒素及其分子生物学研究进展

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5、

Objective To investigate the virulent genes of Shigella spp separated from the patients from Lanzhou city.

目的调查兰州市分离志贺菌株的毒力基因型。

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6、

The contact hemolysis test of Shigella spp

志贺氏菌的接触性溶血试验

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7、

Study on the Distribution and Drug Resistance in 663 strains of Shigella spp

663株志贺氏菌流行分布及耐药性变迁的实验研究

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8、

Methods MRI evaluations were done in 20 children with mitochondrial encephalomyopathy proved by muscle biopsy and biochemical laboratory examinations.

方法20例由肌肉活检及实验室检查证实为线粒体脑肌病的患儿，脑内均有MRI阳性表现，研究其MRI表现的类型。

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9、

But the definite diagnosis of mitochondrial encephalomyopathy depends on skeletal muscle biopsy and gene examination.

脑MRI是诊断儿童线粒体脑肌病的重要手段，但儿童线粒体脑肌病的确诊有赖于肌肉活检和基因检查。

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10、

MRI appearances and diagnosis of mitochondrial encephalomyopathy in children

儿童线粒体脑肌病的脑部MRI表现与诊断

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11、

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）。

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12、

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。

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13、

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。

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14、

A case of mitochondrial myopathy

线粒体肌病1例

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15、

An ultrastructural study on mitochondrial myopathy

线粒体肌病的电镜图像分析研究

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16、

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

线粒体肌病15例。正常对照15例。

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17、

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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18、

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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19、

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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20、

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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