muscle biopsy
英 [ˈmʌsl ˈbaɪɒpsi]
美 [ˈmʌsl ˈbaɪɑːpsi]
肌活组织检查
双语例句
- Methods Data of34 PM patients were collected, the results of muscle enzymes, electromyography and muscle biopsy were analyzed and compared.
方法收集分析34例多发性肌炎患者的首发临床症状、体征、肌酶谱、肌电图、肌活检结果。 - MMF has been mainly detected by deltoid muscle biopsy in adult patients, although it has also been detected by quadriceps muscle biopsy in3 young children.
MMF主要通过三角肌活检在成人患者中发现，但也在3例幼童中通过四头肌活检发现了MMF。 - 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 - We'd have to do a muscle biopsy.
我们要做一个肌肉活组织检查。 - A muscle biopsy is positive for fungus.
肌肉活组织检查发现有真菌侵犯。 - Objective To analyze the clinical features and change of electromyography and muscle biopsy in polymyositis ( PM) and guide diagnosis.
目的总结和分析多发性肌炎患者的临床特征、肌肉电生理及病理改变的临床意义，指导临床诊治。 - The patients who did the muscle biopsy or needle biopsy did not develop any complications.
进行了肌肉活检或针刺活检的所有患者均未发生任何并发症。 - 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 - 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。 - BACKGROUND: Muscle biopsy is an important method in diagnosis of idiopathic inflammatory myopathy ( IM).
背景：肌肉活检病理是诊断特发性炎症性肌病（inflammatorymyopathies，IM）的重要手段。 - 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。 - Ten patients received the muscle biopsy, which showed inflammation in 7 cases ( 70%).
12例活动期肌炎患者中10例行肌肉活检，7例有肌炎改变，占70%（灵敏度）。 - 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。 - 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 - 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。 - Electromyogram and muscle biopsy are helpful in diagnosis of this disease.
肌电图和肌活检对诊断具有重要意义。 - 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。 - Muscle biopsy of him showed a large amount of Red-Ragged ( RR) fibers and abnormal mitochondria.
肌肉活组织检查可见大量不整红边纤维和异常线粒体。 - EMG revealed myogenic damage and there was abnormal muscle biopsy.
EMG示肌源性改变，肌活检异常。 - Patients had abnormal mitochondrial in muscle biopsy.
7例行肌活检均见异常线粒体堆积； - 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。 - 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。 - 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。 - Objective To investigate clinical manifestations and pathological changes of sarcoidosis and the effect of skeletal muscle biopsy in the diagnosis.
目的研究结节病的临床与病理特征及骨骼肌活检在结节病诊断中的作用。 - 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。 - Muscle biopsy showed red ragged fibre and abnormal mitochondria in 2 cases.
2例肌活检可见RRF和异常线粒体。 - 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。 - Methods: Pedigree investigation and pathological examination in the muscle biopsy of proband and his aunt were carried out.
方法：对该家系进行家系调查，对先证者及其姑母进行肌活检组织学观察。 - Muscle biopsy is needed, when clinical manifestation is not typical, muscle pathologic examination can make a definite diagnosis of JDM and identify other causes of myopathy.
当临床表现不典型时需行肌活检，肌肉病理是确诊JDM和鉴别其他原因所致肌病的重要依据。