Objective To explore the genetic pathogenesis of hypokalemic periodic paralysis ( HOKPP), an autosomal dominant disease by detecting gene mutation at related loci.

Thyrotoxic periodic paralysis ( TPP) is a complication of hyperthyroidism. The development of TPP has evident discrepancy of sex and race of people, its onset is due to the interaction of genetic factor and environmental factor.

甲亢性周期性麻痹（TPP）是甲亢的一种合并症，其发生存在着明显的性别和种族差异，由于遗传因素与环境因素相互作用而发病。

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Methods Blood potassium, NO and NOS were measured in patients with hypokalemic periodic paralysis during paralysis stroke and after muscle power recovered.

方法低钾型周期性麻痹患者，在弛缓性瘫痪发作期及肌力恢复后，同时检测血钾、NO、一氧化氮合酶（NOS）。

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This is to study the clinical features of thyrotoxic periodic paralysis ( TPP) caused by Graves ′ disease.

目的探讨Graves病所致甲亢性周期性麻痹（TPP）临床特点。

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

目的探讨低钾型周期性麻痹的心电图（ECG）改变与心肌酶谱变化。

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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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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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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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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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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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The contact hemolysis test of Shigella spp

志贺氏菌的接触性溶血试验

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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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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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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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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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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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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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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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A case of mitochondrial myopathy

线粒体肌病1例

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An ultrastructural study on mitochondrial myopathy

线粒体肌病的电镜图像分析研究

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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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