肌萎缩侧索硬化
神经影像学
医学
痴呆
失智症
心理学
物理医学与康复
重症监护医学
精神科
疾病
病理
作者
Amy Brodtmann,Matthew C. Kiernan
出处
期刊:Neurology
[Ovid Technologies (Wolters Kluwer)]
日期:2013-01-17
卷期号:80 (7): 606-607
被引量:1
标识
DOI:10.1212/wnl.0b013e318281cd27
摘要
Paradigm shifts are occurring across the realm of amyotrophic lateral sclerosis (ALS). In the past, we instructed medical students that ALS was solely a clinical diagnosis; that careful clinical examination raised the specter of this devastating condition, and neurophysiologic testing provided confirmation. We taught that ALS was an isolated clinical syndrome; that neuroimaging was not helpful for the diagnosis, other than to exclude mimic syndromes; that patients did not have significant dementia; and finally, that little could be done to predict or alter an individual patient's course.
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