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- BACKGROUND:Recently, there are two main methods for the assay of Duchenne type muscular dystrophy(DMD):Southern blotting and polymerase chain reaction(PCR). While several limitations are found in the practice. 背景:目前对Duchenne型肌营养不良(DMD)基因缺失的检测主要是Southern印迹或聚合酶链反应(PCR)的方法,在实际应用中有一定的局限性。
- limb girdle type muscular dystrophy 肢带型肌营养不良
- limb-girdle type muscular dystrophy 肢带型肌营养不良
- facio scapulo humeral type muscular dystrophy 面肩肱型肌营养不良
- facio-scapulo-humeral type muscular dystrophy 面肩肱型肌营养不良
- Duchenne's type muscular dystrophy 杜兴(氏)型肌营养不良
- Misdiagnosed case analyses: Duchenne type muscular dystrophy was erroneously diagnosed as hepatitis 进行性肌营养不良误诊断为病毒性肝炎的分析
- Objective To establish a normative procedure for clinical prenatal gene diagnosis of Duchenne and Becker muscular dystrophy(DMD/BMD). 目的 建立规范的假肥大型肌营养不良症 (DMD/BMD)产前基因诊断程序。
- Individuals with Duchenne muscular dystrophy usually lack dystrophin completely while thosewith Becker muscular dystrophy have dystrophinof an altered size. 是最常见的一类进行性肌营养不良症。
- She was the poster child for muscular dystrophy. 她是海报上那个患肌肉萎缩的小孩。
- Gowers type muscular dystrophy 高尔斯(氏)型肌营养不良:同late distal hereditary myopathy
- Objective To explore the value of immunofluorescent technique for clinical diagnosing Duchenne muscular dystrophy(DMD),Becker muscular dystrophy(BMD) and Limb-girdle muscular dystrophy(LGMD). 目的探讨免疫荧光检测对Duchenne型、Becker型和肢带型肌营养不良症(DMD、BMD和LG-MD)临床诊断的价值。
- Methods Dystrophin in the muscle tissue of 12 patients with Duchenne muscular dystrophy (DMD), 5 patients with Becker muscular dystrophy (BMD) was analysed by immunohistochemistry,and compared with muscle tissue of 6 patients without neuromuscle disease. 方法 运用免疫组化法对 12例 Duchenne型肌营养不良症 (DMD)患者及 5例 Becker型肌营养不良症 (BMD)患者的肌组织中肌营养不良蛋白的表达进行分析 ,并用 6例非神经肌肉疾病患者的肌组织作为对照。
- The method of STR sequence polymorphism analysis can determine haplotypes at normal status or at risk status, it would be used in prenatal diagnosis and carrier detection in the families of Duchenne and Becker muscular dystrophy. 短串联重复顺序多态性分析方法可以准确而迅速地区分正常及风险单体型,可用于Duchenne型或Becker型肌营养不良家系中检出携带者及产前诊断
- It’s missing in Duchenne muscular dystrophy, a severe, childhood-onset form of MD, and deficient in Becker MD, a somewhat less severe form of the disease that can begin in childhood or later. 该实验是由他与一家私人的生物技术公司共同进行的，他也是这家公司的共同创立者和首席科学顾问。
- Methods: Fourteen boys with Duchenne or Becker muscular dystrophy, 6 to 11 years old, completed two treatment periods (albuterol and placebo), 12 weeks each, separated by a 12-week washout period. 基于沙丁胺醇缓释剂治疗肌营养不良症患儿的前期研究，作者进行了一项随机、双盲、安慰剂对照的交叉设计的研究。
- What is neuromuscular disease and muscular dystrophy? 什么是神经肌肉疾病和肌肉萎缩症?
- Duchenne muscular dystrophy and Becker's muscular dystrophy are caused by mutations of the gene for the dystrophin protein and lead to an overabundance of the enzyme creatine kinase . 杜氏肌营养不良和贝克尔的肌营养不良症是由基因突变基因的抗肌萎缩蛋白，并导致过多的酶肌酸磷酸激酶。肌营养不良蛋白基因是最大的人类基因。
- 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
- Bell palsy (a type of neuritis) paralyzes the muscles of one side of the face. Muscular dystrophy causes paralysis by attacking muscle. 贝尔氏麻痹(神经炎的一种)引起面部一侧的肌肉瘫痪。肌营养不良侵袭肌肉也能导致瘫痪。
