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- Myoplegic dystrophy 肌麻痹性营养不良
- Of, relating to, or afflicted with dystrophy. 营养不良的营养不良的、与之有关的或患有营养不良症的
- She can't eat and become dystrophy. 她无法进食而变得营养不良。
- 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?
- Objective To summarize the clinical characteristics of myotonic dystrophy (DM). 摘要目的总结强直性肌营养不良症(DM)的临床特点。
- 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。
- In fleck corneal dystrophy,the lesion only involved stroma,epithelium and endothelium levels were normal. 斑点状角膜营养不良病变仅累及基质层,而角膜上皮层及内皮层正常;
- 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。
- 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
- 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 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。
- Objective Improving the detection of gene deficiency in Duchenne/Becker muscular dystrophy(DMD/BMD) patients. 目的 检测假肥大型肌营养不良 (DMD/BMD)基因缺失及提高缺失检出率。
- Objective To analyse the locations and types of gene deletions in Duchenne/Becker muscular dystrophy(DMD/BMD). 目的分析迪谢内/贝克肌营养不良症（DMD/BDM）基因缺失类型及其分布规律。
- Objective To detect dystrophin gene deletion of Duchenne muscular dystrophy (DMD) and make DMD gene diagnosis. 目的探讨Duchenne型肌营养不良症（DMD）患者基因缺失的突变特点并进行基因诊断。
- Objective To investigate the effects of Duchenne muscular dystrophy mice(mdx) treated with stem cells transplantation. 目的 研究骨髓干细胞移植治疗Duchenne型肌营养不良鼠 (mdx鼠 )的效果。
- Objective To perform prenatal diagnosis in 20 families with Duchenne/Becker muscular dystrophy (DMD/BMD). 目的对20个迪谢内/贝克肌营养不良症（DMD/BMD）家系进行产前基因诊断。
- Objective To perform early and presymptomatic diagnosis for facioscapulohumeral muscular dystrophy (FSHD). 目的对面肩肱型肌营养不良症(FSHD)进行早期诊断和症状前诊断。
- Detection deleted Duchenne muscular dystrophy carriers by fluorescence quantitative polymerase chain reaction. 应用荧光定量PCR检测缺失型DMD携带者的研究
