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- benign congenital muscular dystrophy syndrome 良性先天性肌营养不良综合征
- congenital muscular dystrophy(CMD) 先天性肌营养不良症
- Analysis of genotype and phenotype in Fukuyama congenital muscular dystrophy 福山型先天性肌营养不良基因型和表型分析
- Keywords Fukuyama congenital muscular dystrophy;haplotype;genotype;phenotype; 关键词福山型先天性肌营养不良;单体型;基因型;表型;
- congenital muscular dystrophy 先天性肌营养不良症
- She was the poster child for muscular dystrophy. 她是海报上那个患肌肉萎缩的小孩。
- What is neuromuscular disease and muscular dystrophy? 什么是神经肌肉疾病和肌肉萎缩症?
- C-MMD Congenital myotonic muscular dystrophy 先天肌强直性营养不良
- Diseases like multiple sclerosis, muscular dystrophy or polio can leave people disabled. 像多发性硬化症、肌肉萎缩症或小儿麻痹症等疾病会使人残疾。
- congenital atonic sclerotic muscular dystrophy 先天性弛缓硬化性肌营养不良
- Congenital hereditary muscular dystrophy 先天性遗传性肌营养不良
- Any of several disorders,especially muscular dystrophy,in which the muscles weaken and atrophy. 营养障碍任一种机能紊乱,尤指肌肉营养障碍引起的肌肉衰弱和萎缩。
- It will bring cures a step closer for Alzheimer's and Parkinson's disease, diabetes, muscular dystrophy and heart disease. 它将进一步促进对阿尔滋海默症,帕金森症,糖尿病,肌肉萎缩症和心脏病等疾病的治疗。
- Objective: To Discuss the effect of the congenital muscular torticollis (CMT) corrective operation. 目的:探讨先天性肌性斜颈的手术治疗方法。
- Introduction: Congenital muscular torticollis (CMT) is the common disease among newborn. 摘要背景:先天性肌肉斜颈为新生儿常见的疾病。
- Any of several disorders, especially muscular dystrophy, in which the muscles weaken and atrophy. 营养障碍任一种机能紊乱,尤指肌肉营养障碍引起的肌肉衰弱和萎缩
- Objective To review the states of etiological and pathologic research on congenital muscular torticollis(CMT). 目的综述先天性肌性斜颈的病因、发病机理及病理的研究现状。
- The behavioral investigation on Duchenne muscular dystrophy animal model after marrow transplantation. 型肌营养不良模型鼠骨髓移植后的行为学观察。
- Objective: To study the effect of chymotrypsin iontophoresis on congenital muscular torticollis (CMT) of infants. 摘要目的:观察糜蛋白酶离子导入治疗对改善先天性肌性斜颈患儿颈部活动的治疗作用。
- Objective: To identify the deletions in Duchenne/Becker muscular dystrophy (DMD/BMD) by using fluorescence in situ hybridization (FISH). 目的:应用荧光原位杂交(FISH)筛查技术检测假性肥大型肌营养不良症(DMD/BMD)缺失型携带者。