2023年8月8日 · Myasthenia gravis (MG) is the most common disorder affecting the neuromuscular junction (NMJ) of the skeletal muscles. The classic presentation is a fluctuating weakness that is more prominent in the afternoon. It usually involves muscles of …

重症肌无力（myasthenia gravis，MG）是由自身抗体介导的获得性神经-肌肉接头（neuromuscular junction，NMJ）传递障碍的自身免疫性疾病。 乙酰胆碱受体（acetylcholine receptor，AChR）抗体是最常见的致病性抗体…

Myasthenia gravis is an autoimmune disease of the neuromuscular junction (NMJ) caused by antibodies that attack components of the postsynaptic membrane, impair neuromuscular transmission, and lead to weakness and fatigue of skeletal muscle. This can ...

2017年12月21日 · Generalized myasthenia gravis (gMG) is a rare autoimmune disorder characterized by skeletal muscle weakness caused by disrupted neurotransmission at the neuromuscular junction (NMJ). Approximately 74–88% of patients with gMG have acetylcholine receptor (AChR) autoantibodies.

【摘要】 重症肌无力（mg）是一种由自身抗体介导的神经‑肌肉接头（nmj）信号传递障碍的获得 性自身免疫性疾病。自身抗体检测是国内外mg诊治指南推荐的关键辅助诊断指标。mg自身抗体

2023年9月5日 · Myasthenia gravis (MG) is an autoimmune neuromuscular disorder in which antibodies (Abs) target specific proteins involved in the neuromuscular junction function (NMJ) [1]. These mechanisms lead to impaired NMJ transmission, resulting in fluctuating muscle weakness and increased susceptibility to fatigue [1].

重症肌无力(mg)是一种导致神经肌肉接头(nmj)损伤的自身免疫性疾病，其特征是不同骨骼肌区域的运动时虚弱和易疲劳。 MG自身免疫攻击的自身抗体主要是靶向关键功能和结构NMJ蛋白，包括乙酰胆碱受体(AChR)、肌肉特异性…

重症肌无力（Myasthenia Gravis，MG）是一种影响神经与肌肉之间信号传递的自身免疫性疾病。MG的发病机制涉及自身抗体攻击神经肌肉接头（NMJ），这是神经细胞与肌肉细胞之间传递信号的地方。

2023年8月14日 · 重症肌无力（mg）是一种由自身抗体介导的神经-肌肉接头（nmj）信号传递障碍的获得性自身免疫性疾病。 临床表现为全身骨骼肌波动性无力与易疲劳，活动后加重，休息后好转。

2024年8月29日 · Myasthenia Gravis (MG) is a heterogenous neuromuscular junction (NMJ) disorder in which the body elicits an autoimmune response against postsynaptic acetylcholine receptors. It is clinically characterized by fluctuating skeletal muscle weakness (without sensory or autonomic dysfunction) and fatigability and has a predilection for oculobulbar ...