过去50年的重症肌无力研究——个人观点

A. Vincent
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引用次数: 0

摘要

重症肌无力(MG)的研究,在许多方面,是一个开拓者,为越来越多的自身抗体介导的疾病,影响神经系统。对MG的理解在20世纪70年代取得了突破,甚至在50年后,MG仍然是科学家,临床医生和最近的制药公司作为最常见和研究最充分的疾病而回归的主题。在这里,我们将简要回顾一些主要的发现,重点是在发现乙酰胆碱受体抗体后的最初几十年里,人们对这种疾病的认识是如何演变的。应该指出的是,这是一个个人的观点,而不是一个系统的或充分参考审查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myasthenia research over the last 50 years – a personal perspective
Myasthenia gravis (MG) research has, in many respects, been a trail blazer for the growing number of autoantibody-mediated disorders that affect the nervous system. The breakthroughs in MG understanding were made in the 1970s and even 50 years later, MG still remains a topic which scientists, clinicians and, most recently Pharma, return to as the most common and well-studied disorder.  Here, some of the main discoveries will be reviewed very briefly focusing on how the knowledge of the disease evolved during the first decades after the discovery of acetylcholine receptor antibodies.  It should be noted that this is a personal perspective and not a systematic or fully referenced review.
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