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- lipodystrophic myopathy 脂肪代谢障碍性肌病
- Such myopathy appeared within an age range of 40 to 60 years. 原发性的轴性肌病,病因不明,十分罕见。
- Electromyogram of right lamb and left leg demonstrated myopathy. 肌电图示右肱二头、左股直肌、右三角肌肌源性损害;
- 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。
- Foundation of rat steroid myopathy model and its myopathological study. 类固醇肌病大鼠模型的建立及其骨骼肌病变的形态学研究。
- Very rarely, this myopathy leads to muscle breakdown and fatal kidney failure. 非常罕见的，这种肌病会导致肌溶解和致死性肾衰。
- Myopathy occurs in fewer than one in 10 000 patients at these standard doses. 给予标准剂量时，肌肉病的发生率低于万分之有。
- 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。
- Myopathy and the concurrent administration of corticosteroids and neuromuscular blockers are well described in the intensive care unit (ICU) setting. 在ICU，肌病与同时给予皮质类固醇和神经肌肉阻滞剂被详细记录。
- Patients with myopathy remained in the ICU longer than unaffected patients or controls. ICU里的肌病患者比不受影响患者或对照者保持时间长。（不通顺啊！?）
- Objective To investigate the clinical manifestations and pathological features of nemaline myopathy (NM). 目的探讨杆状体肌病的临床表现和病理特点。
- In fact, the combined use of these drugs carries a greater risk for myopathy than does each drug separately. （事实上，联合应用这些药物比单独应用有更高的出现肌病的风险。）
- Objective To study 20 cases of lipid storage myopathy (LSM) and to analyze them in clinical and pathological fields. 目的从临床和肌肉病理的角度分析脂质沉积性肌病(LSM)的特点。
- Some nucleoside and nucleotide analogues may cause renal toxicity, myopathy, and/or mitochondrial toxicity. 有些核甘和核甘类似物可能会引起肾脏毒性、肌肉病变和/或粒腺体毒性。
- Objective The clinical manifestation and prognosis of heart involvement of myopathy were studied. 目的探讨肌病时心肌损害的表现及预后。
- 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。
- Acute myopathy is a cause of weakness in a variety of critically ill patients, including transplant recipients. 急性肌病是一种发生在各种重症患者、导致无力的原因，包括移植受者。
- They compared the 98 patients who developed myopathy with 98 patients who did not. 他们比较了98位出现肌病和98位没有出现肌病的患者。
- Objective:To investigate the clinical and pathological features of Lipid storage myopathy(LSM). 目的:探讨脂质沉积性肌病(LSM)的临床和肌肉病理特点。
- Myotonia seems to originate in the muscles (myopathy) rather than the nervous system. 病变似乎是在肌肉本身，而不是在神经系统。
