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Duchenne muscular dystrophy is a common motal X - Linked recessive disease, whose incidence of male birth is 1/3500. It characterized by progressivelymuscular atrophy and weakness. Duchenne型肌营养不良症(DMD)，是一种严重致死性X连锁隐性遗传病，发病率约为1/3500活男婴，其临床表现以肌肉的进行性萎缩和无力为特征。
Muscular atrophy of a person affected with paralysis. 因麻痹而导致人体肌肉萎缩
Individual local myasthenia gravis patients, muscular atrophy. 个别患者出现局部肌无力、肌萎缩。
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 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。
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。
Investigation and Analysis on Fertility Condition of Female Carriers from 23 Families of Duchenne Muscular Dystro- phy. 23例假肥大型肌营养不良患者家系中女性生育情况的调查与分析
Duchenne muscular dystrophy (DMD): A quantitative study of type 2C fibers and muscle satellite cells. Duchenne型肌营养不良症:2c型纤维与肌卫星细胞的定量研究
Duchenne muscular dystrophy(DMD) takes up 75%(12 cases) in 16 PMD cases,which slightly higher than reference reported. 本组16例PMD中DMD占75%25(12/16),比文献报道稍高[2];
AVI's lead drug candidate, AVI-4658, is in clinical development for Duchenne Muscular Dystrophy. 阿维的领先候选药物，阿维- 4658，是在杜氏肌营养不良症的临床开发。
Objective This paper was designed to investigate the feasibility of non invasive prenetal diagnosis of Duchenne muscular dystrophy(DMD). 目的探讨杜氏肌营养不良症 (Duchenne muscular dystrophy,DMD)的无创性产前基因诊断的可行性。
Objective To study affected muscle selectivity and main laboratorial examination value of duchenne muscular dystrophy(DMD). 目的探讨Duchenne型肌营养不良症(DMD)受累肌肉的选择性及各项实验室检查的诊断价值。
Objective To study prenatal gene diagnosis in high danger pregnant wo men with Duchenne muscular dystrophy (DMD) families. 目的研究Duchenne肌营养不良症（DMD）家系中高风险孕妇的产前基因诊断。
Objective:To observe bone marrow rebuilding after bone marrow transplantation (BMT) to treat Duchenne muscular dystrophy (DMD). 目的:观察在骨髓移植(bonemarrowtransplantation,BMT)治疗Duchenne型肌营养不良症(DMD)模型鼠mdx鼠后,骨髓重建过程及目的蛋白的表达情况。
To explore the application of erythrocyte of freeze-fracture electron microscopy in the diagnosis of carriers of Duchenne muscular dystrpphy (DMD). 探讨红细胞冷冻断裂电镜术在Duchenne型肌营养不良症基因携带者诊断中的应用。
First of all, mutation analysis of Duchenne muscular dystrophy (DMD) gene was carried out by CE coupled with multi-PCR technique. 在医学领域主要表现为以基因突变检测，基因家系连锁分析，特定基因的PCR产物直接检测为基础的基因诊断。
Approximately one in every 3,500 boys worldwide is afflicted with Duchenne muscular dystrophy with 20,000 new cases reported each year. 大约每3500男孩全世界患有杜氏肌营养不良的20000新病例每年报告。
Dystrophin, the protein missing in Duchenne muscular dystrophy patients, conducts this energy across the muscle cell's membrane, protecting the fiber. 但肌节产生的力量，如果没有向外引导的话，也会伤害肌纤维，DMD患者所缺乏的肌肉萎缩蛋白，能将这股力量传导到肌肉细胞膜上，而保护肌纤维。