重症肌无力是乙酰胆碱受体抗体介导、细胞免疫依赖、补体参与的自身免疫性疾病。
Myasthenia gravis(MG) is an autoimmune disease which choline receptor antibody mediates, cell immunity depends on and addiment participates.
皮疹的出现有时是肌无力的先兆。
重症肌无力是一种较难治疗的疾病。
此型患者可伴眼外肌无力或轻度四肢肌无力。
This type of patient may be associated with extraocular muscle weakness or mild limb weakness.
目的探讨眼肌型重症肌无力的临床特点及治疗。
Objective To observe the clinical manifestations and treatment of ocular myasthenia gravis.
律师：你所患的重症肌无力会影响你的记忆力吗？
ATTORNEY: : This myasthenia gravis, does it affect your memory at all?
结论外科手术是治疗重症肌无力危象的方法之一。
Conclusion Emergency thymectomy is the treatment of choice for crisis of myasthenia gravis.
目的：探讨重症肌无力及其危象的有效护理措施。
Objective: To explore the effect of nursing measures for myasthenia gravis and it's crisis.
方法对81例重症肌无力患者的死因进行回顾性分析。
Methods: To do retrospective analysis of death reasons in 81 MG patients.
目的：研究伴胸腺异常重症肌无力（MG）的临床特点。
Objective:To explore the clinical features of myasthenia gravis(MG) with Abnormal thymus gland.
目的：评价胸腺切除术对眼肌型重症肌无力患者的疗效。
Objective: to assess the efficacy of thymectomy for the treatment of ocular myasthenia gravis.
注射肉毒素的副作用包括轻微短暂的肌无力和注射点疼痛。
Side effects included mild and temporary muscle weakness and pain at the injection site.
重症肌无力是一种神经肌肉疾病，主要症状是犬只全身虚弱。
Myasthenia gravis is a neuromuscular disease where the primary symptom is weakness in various body parts of the dog.
方法：回顾并分析胸腺切除术后并发肌无力危象7例临床资料。
Method 7 cases of clinical data about myasthenia gravis crisis after thymectomy were retrospected and analyzed.
然而，老年犬发生重症肌无力时，一般被认为是免疫介导的疾病。
However, when myasthenia gravis occurs in older dogs it is thought of as an immune-mediated disease.
他们的产品可以帮助那些肌无力或身患残疾的使用者来操作电脑。
Their product enables users, who have weak muscles or are disabled, to operate a computer.
目的探讨胸腺瘤合并重症肌无力（MG）扩大根治术术式的疗效。
Objective: To investigate the effect of thymomas with myasthenia gravis(MG) treated by extensive radical resection.
目的探讨肘肌重复神经刺激(RNS)对重症肌无力的诊断价值。
Objective Repetitive nerve stimulation of anconeus muscle (anconeus RNS) was explored in diagnosis of myasthenia gravis.
多数患者在四肢肌无力起病后数月至数年迅速衍变为全身肌无力。
Most of the patients after the onset of muscle weakness in the limbs for several months to several years of rapid evolvement for the whole body weakness.
结论TNF基因多态性与胸腺瘤发病及胸腺瘤发生重症肌无力相关。
Conclusion: TNF gene may be correlated with the susceptibility of thymoma and thymoma with MG.
背景全髋关节置换术后外展肌无力是个罕见但易导致功能不佳的问题。
Background Abductor mechanism insufficiency after total hip arthroplasty is a rare but debilitating problem.
结论小儿重症肌无力的病史和新斯的明试验阳性是诊断本病的重要依据。
Conclusion Medical history of infantile myasthenia gravis and positive of neostigmine test are important diagnostic bases of this disease.
目的观察血浆置换联合小剂量激素治疗重症肌无力的临床疗效及安全性。
Objective To explore the therapeutic effects of blood plasma replacement and small dose hormone on myasthenia gravis (MG).
晚发式蓬佩病的特性是进行性肌无力和呼吸功能丧失，从而导致早期死亡。
Late-onset Pompe's disease is characterized by progressive muscle weakness and loss of respiratory function, leading to early death.
肌病患者通常会有肌痛、肌无力的症状，同时血中肌酶(肌酸激酶)升高。
Patients with myopathy generally have muscle pain, tenderness or weakness, and an elevation of a muscle enzyme in the blood (creatine kinase).
目的研究重症肌无力(MG)患者临床绝对评分和电生理检查结果的相关性。
Objective To investigate the correlation between clinical absolute scores and electrophysiological parameters in patients with myasthenia gravis (MG).
在存在恶性肿瘤的情况下，呼吸功能损害可能发生在肢体近端肌无力出现之前。
In the presence of malignancy, respiratory function may be compromised even when proximal limb muscles remain strong.
目的提高临床医生对青霉胺(D -PA)致肾病综合征和重症肌无力的认识。
Objective To improve clinicians 'understanding of nephrotic syndrome and myasthenia gravis as adverse events of penicillamine (D-PA).
目的研究重症肌无力(MG)患者常规针极肌电图(EMG)表现及其诊断价值。
Objective To investigate the routine needle electromyography (EMG) findings and its diagnostic value in patients with myasthenia gravis (MG).
目的介绍胸骨部分劈开切口行扩大的胸腺切除术治疗重症肌无力的手术方法和效果。
Objective to introduce the surgical method and evaluate the efficacy of extended thymectomy through partial sternotomy for the treatment of myasthenia gravis.
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