进行性脊肌萎缩症
- 网络progressive spinal muscular atrophy;PSMA;SMA;Progressive muscular atrophy
进行性脊肌萎缩症-
运动神经元存活基因对进行性脊肌萎缩症的诊断价值
The diagnosis value of SMN gene deletions in progressive spinal muscular atrophy
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进行性脊肌萎缩症129例临床分析
Clinical analysis of 129 cases of progressive spinal muscular atrophy
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根据病变累及部位及病程可分为许多类型，其中最主要的有肌萎缩侧索硬化（amyotrophiclateralsclerosis，ALS）和进行性脊肌萎缩症（Progressivemuscularatrophy，PMA）。
According to the involved area and illness course , MND can be divided into several types , but amyotrophic lateral sclerosis ( ALS ) and progressive muscular atrophy ( PMA ) are the main types .