1)spinal muscular atrophy脊肌萎缩症
1.Clinical features and inheritance analysis of 23 cases of spinal muscular atrophy;儿童脊肌萎缩症23例临床特点及遗传学分析
2.Prenatal diagnosis of spinal muscular atrophy based on amniotic fluid cells culturing;羊水细胞培养进行脊肌萎缩症的产前诊断
3.Preliminary study on survival motor neuron gene deletion of exon 7 in adult onset patients with spinal muscular atrophy;成年起病脊肌萎缩症SMN基因外显子7缺失的初探
英文短句/例句
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 sclerosisph.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
相关短句/例句
Spinal muscular atrophy脊髓性肌萎缩症
1.Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy;脊髓性肌萎缩症SMN1基因定量研究及基因携带者的筛查(英文)
2.Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography;应用变性高效液相色谱技术快速诊断儿童型脊髓性肌萎缩症(英文)
3.Prenatal diagnosis of spinal muscular atrophy based on umbilical cord blood;胎儿脐带血产前诊断脊髓性肌萎缩症
3)Amyotrophic lateral sclerosis(ALS)肌萎缩脊髓侧索硬化症
4)childhood-onset spinal muscular atrophy儿童型脊髓性肌萎缩症
1.Prenatal diagnosis in seven families with childhood-onset spinal muscular atrophy;儿童型脊髓性肌萎缩症家系7例产前诊断
5)progressive spinal muscular atrophy进行性脊肌萎缩症
1.Clinical analysis of 129 cases of progressive spinal muscular atrophy;进行性脊肌萎缩症129例临床分析
6)Adult spinal muscular atrophy成人型脊髓性肌萎缩症
延伸阅读
肌萎缩性侧索硬化症肌萎缩性侧索硬化症 一种原因未明的进行性的神经系统变性疾病,可能与遗传、中毒、损伤、感染有关。突出的病理变化为皮质延髓束和皮质脊髓束的变性,脊髓前角细胞以及脑干运动神经核的损害。锥体束的变性最早出现在脊髓比较低的部位,随病程进展,逐渐向高位脊髓及脑干推进。肌肉表现有神经性肌萎缩的典型征象。临床特点为:多数病人发生于30~50岁之间,男性较女性发病率高。患者可有麻木和发凉等感觉异常,肌肉无力,挛缩,肌束颤动及萎缩,持久性腱反射亢进和病理反射,随时间增长,无力症状扩展到躯干及颈部,最后累及面部及延髓支配的肌肉,出现其相应症状和体征。本病无特殊治疗措施。