论文部分内容阅读
重症肌无力(MG)是一种以肌肉无力和易疲劳为特点的神经肌肉性疾病,发病率为1/20,000～1/30,000.1973年Patrick和Lindstrom首先在实验性自身免疫性重症肌无力(EAMG)动物体内检测到
Myasthenia gravis (MG) is a neuromuscular disease characterized by muscle weakness and fatigue with a prevalence of 1 in 20,000 to 1 in 30,000. In 1973, Patrick and Lindstrom first demonstrated the role of a marker in experimental autoimmune myasthenia gravis (EAMG) Animal body detected