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重症肌无力伴胸腺瘤38例病理与临床分析 被引量:4

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摘要 重症肌无力(myasthenia gravis,MG)是一种主要累及神经肌肉接头处突触后膜乙酰胆碱受体的自身免疫性疾病,10%~15%患者伴有胸腺瘤。胸腺瘤的类型、临床分期与MG的发生、发展及转归具有一定关系。笔者将38例伴胸腺瘤MG的病理改变、临床分型。
出处 《武警医学》 CAS 2012年第3期259-261,共3页 Medical Journal of the Chinese People's Armed Police Force
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参考文献10

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共引文献207

同被引文献59

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