期刊
MOVEMENT DISORDERS
卷 24, 期 4, 页码 479-489出版社
WILEY
DOI: 10.1002/mds.22425
关键词
myoclonus-dystonia; primary dystonia; clinical neurology; epsilon-sarcoglycan; genetics; pathophysiology
Our knowledge of the clinical, neurophysiological, and genetic aspects of myoclonus-dystonia (M-D) has improved markedly in the recent years. Basic research has provided new insights into the complex dysfunctions involved in the pathogenesis of M-D. On the basis, of a comprehensive literature search, this review summarizes current knowledge on M-D, with a focus on recent findings. We also propose modified diagnostic criteria and recommendations for clinical management. (C) 2008 Movement Disorder Society
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据