1.
Objective: To assess whether there has been a change in survival in patients with SMA type 1 between 1980 and 2006.
目的：评价1980年至2006年出生的1型脊肌萎缩症幸存者的病程改变。
2.
Detection of the SMN1 deletion by two techniques
应用2种方法检测脊肌萎缩症运动神经元生存基因1缺失
3.
Objective To investigate the relationship between survival motor neuron( SMN) gene and the clinical features of childhood spinal muscular atrophy( SMA).
目的探讨运动神经元存活基因与儿童期脊肌萎缩症临床特征的关系。
4.
Objective This study examined the prevalence of deletion and subtle mutations of survival motor neuron( SMN) gene in children with spinal muscular atrophy( SMA).
目的研究儿童型脊肌萎缩症(MA)者中运动神经元生存基因缺失与微突变情况。
5.
Conclusion: Survival in spinal muscular atrophy type 1 patients has increased in recent years, in relation to the growing trend toward more proactive clinical care.
结论：近年来1型脊肌萎缩症幸存者增加归功于主动临床护理的增长。
6.
amyotrophic lateral sclerosis
ph.1. 肌萎缩性脊髓侧索硬化症
7.
The Studies of the Detection and Expression of SMN Gene of Spinal Muscular Atrophy;
脊髓性肌萎缩症SMN基因检测及其表达的研究
8.
Gene Sequencing and Prenatal Diagnosis of Spinal Muscular Atrophy;
脊髓性肌萎缩症基因测序及产前基因诊断
9.
The Studies and Application of Gene Diagnosis for Spinal Muscular Atrophy;
脊髓性肌萎缩症的基因诊断及其应用研究
10.
progressive spinal muscular atrophy
脊髓性进行性肌萎缩
11.
syphilitic spinal muscular atroph
梅毒性脊髓病性肌萎缩
12.
Analysis of clinical manifestation and EMG in patients with spinal muscular atrophy accompanied by elevation of CK levels
肌酸磷酸激酶增高的脊髓性肌萎缩症患者临床与肌电图分析
13.
Diadynamic value of eletromyography in identification of amyotrophic lateral sclerosis and cervical spondylotic myelopathy
肌电图在鉴别肌萎缩侧索硬化症和脊髓型颈椎病中的诊断价值
14.
He had muscular dystrophy.
他患了肌肉萎缩症。
15.
duchenne muscle dystrophy
杜氏持续性肌肉萎缩症
16.
② nerve conduction velocity of patients with ASL and SCM.
②肌萎缩侧索硬化症与脊髓型颈椎病患者神经传导速度检测结果。
17.
Relationship between Expression of Zinc Finger Protein A20 mRNA and Apoptosis in Spinal Muscular Atrophy;
锌指蛋白A20mRNA表达与脊髓性肌萎缩症细胞凋亡的关系
18.
The Association Analysis between Spinal Muscular Atrophy 1 and Mitochondrial Genome;
I型脊髓性肌萎缩症与线粒体基因组的相关性研究