Amyotrophic lateral sclerosis disease modifying therapeutics: a cell biological perspective
Bor Luen Tang
摘要：Amyotrophic lateral sclerosis (ALS) is a progressively fatal neu-romuscular disorder classically characterized by loss of upper and lower motor neurons from the cortex to the spinal cord. Diagnosed patients have a median survival of about 3 years and death usually results from eventual respiratory failure.
机标关键词：respiratory failuremotor neuronsspinal cord
论文发表日期：2017-01-01
在线出版日期：2025-08-15（本平台首次上网日期，不代表文献的发表时间）
页数：2( 407-408 )