Suppr超能文献

重症肌无力的临床特征。

Clinical features of myasthenia gravis.

作者信息

Hopkins L C

机构信息

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia.

出版信息

Neurol Clin. 1994 May;12(2):243-61.

PMID:8041340
Abstract

Myasthenia gravis (MG) is an antibody-mediated muscle disease in which any skeletal muscle can be affected. MG may produce numerous symptoms and signs. To doctors and patients, it may seem like lung disease, stroke, heart disease, or the effects of emotional stress. This article explores the "territory" between MG and diseases of the heart and lungs as well as the other neuromuscular diseases.

摘要

重症肌无力(MG)是一种由抗体介导的肌肉疾病,任何骨骼肌都可能受到影响。重症肌无力可能会产生许多症状和体征。对医生和患者来说,它可能看似是肺部疾病、中风、心脏病或情绪压力的影响。本文探讨了重症肌无力与心肺疾病以及其他神经肌肉疾病之间的“领域”关系。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验