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limb girdle muscular dystrophy 肢带型肌营养不良
limb girdle type muscular dystrophy 肢带型肌营养不良
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?
The rheumatic polymyalgia has the neck shoulder pain, the limb girdle myo- ache and the myasthenia. 风湿性多肌痛有颈肩痛、肢带肌的疼痛及肌无力。
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。
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。
limb girdle dystrophy of Erb Erb肢带肌萎缩症, Erb假肥大性肌营养不良
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
To explore the application of freeze etching electrom microscopy in the study of Duchenne muscular dystrophy(DMD). 目的：探讨电镜冷冻蚀刻技术在Duchenne 型肌营养不良症（ DMD）研究中的应用。