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- W3030656961 endingPage "788" @default.
- W3030656961 startingPage "786" @default.
- W3030656961 abstract "重症肌无力(myasthenia gravis, MG)是神经肌肉接头(neuromuscular junction, NMJ)的自身免疫病,表现为波动性肌无力症状,亦可有较恒定的体征[1].MG可累及全身骨骼肌,亦可累及平滑肌和心肌,受累肌群的不同使症状丰富多样.其首发症状缺乏特异性,患者肌群运用情况不同也使发现症状的背景不同,给诊断带来困难.MG是可治性疾病,早期诊断和治疗有助于控制发展.应重视MG的临床诊断.我院3100例随访较完善的MG资料总结与国内另一MG中心的大宗报道[2]相近,现结合相关数据和研究进展探讨MG的临床诊断。" @default.
- W3030656961 created "2020-06-05" @default.
- W3030656961 creator A5011646266 @default.
- W3030656961 creator A5013937865 @default.
- W3030656961 date "2006-11-23" @default.
- W3030656961 modified "2023-09-25" @default.
- W3030656961 title "重视重症肌无力的临床诊断" @default.
- W3030656961 doi "https://doi.org/10.3760/j.issn:1006-7876.2006.11.024" @default.
- W3030656961 hasPublicationYear "2006" @default.
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