muscular dystrophy
美 [ˌmʌskjələ 'dɪstrəfi] 
英 [ˌmʌskjələ 'dɪstrəfi]
- n.肌营养不良症；肌肉萎缩
- 网络肌肉萎缩症；肌肉营养不良症；肌肉失养症
英汉双解
1. | 肌营养不良症；肌肉萎缩a medical condition that some people are born with in which the muscles gradually become weaker |
英汉解释
英英解释
例句
Duchenne Muscular Dystrophy (DMD) is one of the most common fatal genetic disorders to affect children around the world.
杜氏肌营养不良（DMD）是最常见的致命的遗传疾病之一，影响到世界各地的儿童。
Duchenne Muscular Dystrophy is a fatal genetic mutation in about one of every 3, 500 boys.
杜氏肌萎缩症是一种致死性的基因突变疾病，平均每3500个男孩中就有一个罹患此病。
She returned to movies in the early 2000s and played a woman with Muscular Dystrophy, which launched her superstardom.
而她重返影坛是在本世纪初，扮演一个患肌营养不良症的妇女，这个角色让她跻身巨星行列。
She was the poster child for muscular dystrophy.
她是海报上那个患肌肉萎缩的小孩。
The drug, known as PTC124, has already had encouraging results in patients with Duchenne muscular dystrophy and cystic fibrosis.
被称为PTC124的药物，已经在治疗Duchenne肌营养不良和囊性纤维化的病人中获得了激动人心的成果。
But it could also make it easier to treat Parkinson's disease, motor neurone disease and muscular dystrophy.
但是，新治疗技术也将使帕金森病、运动神经疾病和肌肉萎缩症的治疗变得简单容易。
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。
He suffers from a rare form of muscular dystrophy, a ventilator supplying his oxygen.
他患有一种罕见的肌失养症，靠吸氧器供氧。
Research into gene therapy may eventually provide treatment to stop the progression of some types of muscular dystrophy.
到基因治疗研究提供治疗最终可能停止恶化的某些类型的肌肉营养不良症。
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。
Since cell growth is a fundamental biological process, the research may shed light on everything from miscarriages to muscular dystrophy.
由于细胞生长是基本生物学过程，该研究将对流产、肌营养失调等各个领域产生影响。
Physical therapy As muscular dystrophy progresses and muscles weaken, fixations (contractures) can develop in joints.
由于肌肉萎缩症的进展和肌肉减弱，录制品（挛缩）可发展的关节。
ABSTRACT: Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
摘要：目的探讨同患假肥大型肌营养不良症（DMD）兄妹的临床以及实验室检查特点。
Recent studies have shown that moderate drinkers of wine can prevent heart disease, cancer, and alzheimer's disease and muscular dystrophy.
最新研究已经证实，适度饮用葡萄酒可以预防心脏病、癌症、老年痴呆以及肌肉萎缩症。
Blood samples are examined for mutations in some of the genes that cause different types of muscular dystrophy.
血液样本进行检查的突变基因在一些引起不同类型的肌肉营养不良症。
Muscular dystrophy is a group of more than 30 genetic diseases, characterized by progressive weakness and deterioration of skeletal muscles.
肌营养不良是30种遗传性疾病的一种，以骨骼肌进展性无力和变性为特点。
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。
We meet one young Taiwanese girl who may suffer from debilitating muscular dystrophy but who isn't afraid to pursue her dreams.
还有我们来认识一位台湾女孩，虽然患有肌肉萎缩症，却没有放弃追逐梦想；
There's currently no cure for any form of muscular dystrophy.
目前没有任何形式的治愈肌肉营养不良症。
Quick movements cause muscle stiffening. There is also a myotonic form of muscular dystrophy.
快速运动会引起肌强直，肌营养不良是另一种肌强直类型。
Specific muscle groups are affected by different types of muscular dystrophy.
特定的肌肉群受到不同类型的肌营养不良症。
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。
AVI's lead drug candidate, AVI-4658, is in clinical development for Duchenne Muscular Dystrophy.
的AVI的领先候选药物，为AVI-4658，是杜氏肌营养不良症在临床开发。
Duchene's muscular dystrophy and cystic fibrosis are examples of hereditary diseases that result from nonsense mutations.
无义突变能导致肌无力和囊肿纤维化等疾病。
Muscular Dystrophy - Drug Pipeline Analysis and Market F. . .
肌营养不良症药品渠道分析及市场预测研究报告。
In 1986, American researchers identified the genetic defect underlying one type of muscular dystrophy.
1986年，研究人员发现了一种因肌肉营养失调导致的遗传缺陷。
Most children with Duchenne muscular dystrophy die in their late teens or early 20s.
多数患进行性假肥大性肌营养不良的儿童可以活到十几岁或20几岁。
Replacing defective genes holds out great promise for people suffering from diseases such as muscular dystrophy and cancer.
通过基因治疗，有缺陷的基因被置换掉，那么像患有肌肉萎缩或癌症的人们就极有可能被治愈。
Muscular dystrophy is a birth defect.
肌肉营养失调只有出生时才会发生
About 13 per cent of patients with Duchenne muscular dystrophy have a nonsense mutation and should respond to the drug.
大约有13%的Duchenne肌营养不良病例是无意义突变，应该对该药有反应。
AbstractObjectiveOur aim is to study the role of tissue inhibitor of metalloproteinase1 (TIMP1) in progressive muscular dystrophy (PMD).
目的探讨金属蛋白酶组织抑制剂1（TIMP1）在进行性肌营养不良（PMD）发病中的作用。
Primary study of CK-MM used to determine the curative effect of muscular dystrophy
CK-MM亚型用于肌营养不良症疗效判定的初步研究
Correlation between electroretinographic findings, clinical phenotypic and genotypic analysis in Duchenne and Becker muscular dystrophy
进行性肌营养不良患者视网膜眼电图表型与临床分型及基因型的关系
Determination of Phospholipids in Erythrocyte Membrane from Duchenne Muscular Dystrophy by High Performance Liquid Chromatography
肌营养不良症患者红细胞膜磷脂组成的高效液相色谱分析
Dystrophin detection by immunofluorescent technique for diagnosing muscular dystrophy
免疫荧光检测抗肌萎缩蛋白诊断肌营养不良症的临床应用
Myoblast transfer treatment for Duchenne muscular dystrophy Cochrane Neuromuscular Disease Group
成肌细胞移植治疗进行性肌营养不良
Analysis of short tandem repeat polymorphism in a female patient with Duchenne muscular dystrophy
非缺失型女性Duchenne型肌营养不良症患者短串联重复序列多态性分析
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
A preliminary study of gene products encoded by disease genes of muscular dystrophy
肌营养不良症致病基因编码产物检测的初步研究
Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy
肌营养不良症患者肌肉中肌营养蛋白与神经元型一氧化氮合酶相互关系的研究
