muscle biopsy

Clinical features, chanses in EMG and muscle biopsy were consistent with HMSN type ⅰ.

其临床表现、EMG和肌活检等改变均符合HMSNⅠ型的特征。

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Clinical analysis on the results of muscle biopsy of 268 cases of hyperthyroidism

268例甲亢病人的肌活检及临床分析

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Electromyogram ( emg) and muscle biopsy in patients with chronic spinal muscular atrophy

慢性脊髓性肌萎缩的肌电图及肌活检

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No typical ragged red fiber and other specific pathological changes were found in muscle biopsy samples of 2 cases.

2例行肌活检者未见破碎样红纤维及其他特异性改变。

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Methods Plasma lactate level measurement, EMG examination, CT brain scan, muscle biopsy and electron microscopy examination.

方法总结临床特点，检测血清乳酸及丙酮酸水平，行肌电图、CT脑扫描、肌活检组织化学染色及电子显微镜超微结构检查。

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Likewise, oxidative activity was not disrupted a muscle biopsy a patient with A.

同样地, A病人的肌肉活检切片显示氧化功能并未受影响.

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Wet weight of triceps surae was measured. The denervated muscle was given HE staining and Mallory staining, while the frozen muscle biopsy tissue was given Immunofluorescence with postsynaptic membrane AchR specific antibody.

测量小腿三头肌肌湿重，并分别应用HE染色、Mallory三色染色的方法对失神经肌肉组织进行染色，同时应用突触后膜乙酰胆碱受体（AchR）特异性抗体对肌肉冰冻切片进行免疫荧光染色。

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Improvement and application of diagnostic techniques of the skeletal muscle biopsy

骨骼肌活组织检查病理诊断技术的改进及应用

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Results There were similarities in serum muscle enzymes, EMG and muscle biopsy between experimental myositis and human polymyositis.

结果发现其与人类多发性肌炎（PM）在肌酶、肌电图（EMG）、病理上的改变有相似之处。

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The clinicopathological changes were investigated by electromyogram ( EMG) and muscle biopsy in 30 cases of chronic spinal muscular atrophy.

对30例慢性肌脊髓性萎缩症患者进行肌电图和肌活检检查。

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Methods: The specimens of muscle biopsy taken from 2 patients were studied with light microscopy and transmission electron microscopy ( TEM).

方法：对2例线粒体肌病患者腓肠肌活检组织进行光镜和电镜超微病理观察。

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methods: data of 134 cases of pm/ dm concerning the initial symptoms, subsequent manifestations, muscle enzymes, electromyogram, muscle biopsy, treatment and prognosis were analyzed retrospectively and compared.

方法：回顾性分析本院134例PM和DM患者的临床首发症状及病程中临床表现、肌酶水平、肌电图、肌活检、治疗以及转归，并对PM和DM进行分析比较。

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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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A muscle biopsy is positive for fungus.

肌肉活组织检查发现有真菌侵犯.

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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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The clinical features and muscle biopsy are essential for diagnosis of the disease.

结论小儿线粒体脑肌病罕见，临床特点及肌肉病理检查是诊断本病的重要根据。

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Muscle biopsy has an important value on the diagnosis and differential diagnosis of this disease.

肌内活检对本病的诊断和鉴别诊断具有重要意义。

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Methods The characteristics of clinical expressions and signs were reported, muscle biopsy was did and pathologic findings and pathogenesis were discussed.

方法报告1例成人晚发型杆状体肌病患者的临床表现、实验室及肌肉病理检查，结合国内外文献进行病理改变及发病机制方面的讨论。

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ATP staining revealed isotype muscle grouping and muscle fibre compensative hypertrophy. CONCLUSION: Muscle biopsy has significances in diagnosis and differentiation of adult spinal muscular atrophy.

结论：肌活检对成人型脊髓性肌萎缩症具有诊断和鉴别诊断意义。

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Likewise, oxidative activity was not disrupted in a muscle biopsy specimen from a patient with CMT 2 A.

同样地, CMT2A病人的肌肉活检切片显示氧化功能并未受影响.

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