muscular dystrophy
美 [?m?skj?l? 'd?str?fi] 
英 [?m?skj?l? 'd?str?fi]
- n.肌營養不良癥；肌肉萎縮
- 網絡肌肉萎縮癥；肌肉營養不良癥；肌肉失養癥
英漢雙解
1. | 肌營養不良癥；肌肉萎縮a medical condition that some people are born with in which the muscles gradually become weaker |
英漢解釋
英英解釋
例句
Duchenne Muscular Dystrophy (DMD) is one of the most common fatal genetic disorders to affect children around the world.
杜氏肌營養不良（DMD）是最常見的致命的遺傳疾病之一，影響到世界各地的兒童。
Duchenne Muscular Dystrophy is a fatal genetic mutation in about one of every 3, 500 boys.
杜氏肌萎縮癥是一種致死性的基因突變疾病，平均每3500個男孩中就有一個罹患此病。
She returned to movies in the early 2000s and played a woman with Muscular Dystrophy, which launched her superstardom.
而她重返影壇是在本世紀初，扮演一個患肌營養不良癥的婦女，這個角色讓她躋身巨星行列。
She was the poster child for muscular dystrophy.
她是海報上那個患肌肉萎縮的小孩。
The drug, known as PTC124, has already had encouraging results in patients with Duchenne muscular dystrophy and cystic fibrosis.
被稱為PTC124的藥物，已經在治療Duchenne肌營養不良和囊性纖維化的病人中獲得了激動人心的成果。
But it could also make it easier to treat Parkinson's disease, motor neurone disease and muscular dystrophy.
但是，新治療技術也將使帕金森病、運動神經疾病和肌肉萎縮癥的治療變得簡單容易。
Bell palsy (a type of neuritis) paralyzes the muscles of one side of the face. Muscular dystrophy causes paralysis by attacking muscle.
貝爾氏麻痹（神經炎的一種）引起面部一側的肌肉癱瘓。肌營養不良侵襲肌肉也能導致癱瘓。
He suffers from a rare form of muscular dystrophy, a ventilator supplying his oxygen.
他患有一種罕見的肌失養癥，靠吸氧器供氧。
Research into gene therapy may eventually provide treatment to stop the progression of some types of muscular dystrophy.
到基因治療研究提供治療最終可能停止惡化的某些類型的肌肉營養不良癥。
The behavioral investigation on Duchenne muscular dystrophy animal model after marrow transplantation.
型肌營養不良模型鼠骨髓移植后的行為學觀察。
Since cell growth is a fundamental biological process, the research may shed light on everything from miscarriages to muscular dystrophy.
由于細胞生長是基本生物學過程，該研究將對流產、肌營養失調等各個領域產生影響。
Physical therapy As muscular dystrophy progresses and muscles weaken, fixations (contractures) can develop in joints.
由于肌肉萎縮癥的進展和肌肉減弱，錄制品（攣縮）可發展的關節。
ABSTRACT: Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
摘要：目的探討同患假肥大型肌營養不良癥（DMD）兄妹的臨床以及實驗室檢查特點。
Recent studies have shown that moderate drinkers of wine can prevent heart disease, cancer, and alzheimer's disease and muscular dystrophy.
最新研究已經證實，適度飲用葡萄酒可以預防心臟病、癌癥、老年癡呆以及肌肉萎縮癥。
Blood samples are examined for mutations in some of the genes that cause different types of muscular dystrophy.
血液樣本進行檢查的突變基因在一些引起不同類型的肌肉營養不良癥。
Muscular dystrophy is a group of more than 30 genetic diseases, characterized by progressive weakness and deterioration of skeletal muscles.
肌營養不良是30種遺傳性疾病的一種，以骨骼肌進展性無力和變性為特點。
Objective To perform early and presymptomatic diagnosis for facioscapulohumeral muscular dystrophy (FSHD).
目的對面肩肱型肌營養不良癥（FSHD）進行早期診斷和癥狀前診斷。
We meet one young Taiwanese girl who may suffer from debilitating muscular dystrophy but who isn't afraid to pursue her dreams.
還有我們來認識一位臺灣女孩，雖然患有肌肉萎縮癥，卻沒有放棄追逐夢想；
There's currently no cure for any form of muscular dystrophy.
目前沒有任何形式的治愈肌肉營養不良癥。
Quick movements cause muscle stiffening. There is also a myotonic form of muscular dystrophy.
快速運動會引起肌強直，肌營養不良是另一種肌強直類型。
Specific muscle groups are affected by different types of muscular dystrophy.
特定的肌肉群受到不同類型的肌營養不良癥。
It will bring cures a step closer for Alzheimer's and Parkinson's disease, diabetes, muscular dystrophy and heart disease.
它將進一步促進對阿爾滋海默癥，帕金森癥，糖尿病，肌肉萎縮癥和心臟病等疾病的治療。
AVI's lead drug candidate, AVI-4658, is in clinical development for Duchenne Muscular Dystrophy.
的AVI的領先候選藥物，為AVI-4658，是杜氏肌營養不良癥在臨床開發。
Duchene's muscular dystrophy and cystic fibrosis are examples of hereditary diseases that result from nonsense mutations.
無義突變能導致肌無力和囊腫纖維化等疾病。
Muscular Dystrophy - Drug Pipeline Analysis and Market F. . .
肌營養不良癥藥品渠道分析及市場預測研究報告。
In 1986, American researchers identified the genetic defect underlying one type of muscular dystrophy.
1986年，研究人員發現了一種因肌肉營養失調導致的遺傳缺陷。
Most children with Duchenne muscular dystrophy die in their late teens or early 20s.
多數患進行性假肥大性肌營養不良的兒童可以活到十幾歲或20幾歲。
Replacing defective genes holds out great promise for people suffering from diseases such as muscular dystrophy and cancer.
通過基因治療，有缺陷的基因被置換掉，那么像患有肌肉萎縮或癌癥的人們就極有可能被治愈。
Muscular dystrophy is a birth defect.
肌肉營養失調只有出生時才會發生
About 13 per cent of patients with Duchenne muscular dystrophy have a nonsense mutation and should respond to the drug.
大約有13%的Duchenne肌營養不良病例是無意義突變，應該對該藥有反應。
AbstractObjectiveOur aim is to study the role of tissue inhibitor of metalloproteinase1 (TIMP1) in progressive muscular dystrophy (PMD).
目的探討金屬蛋白酶組織抑制劑1（TIMP1）在進行性肌營養不良（PMD）發病中的作用。
Primary study of CK-MM used to determine the curative effect of muscular dystrophy
CK-MM亞型用于肌營養不良癥療效判定的初步研究
Correlation between electroretinographic findings, clinical phenotypic and genotypic analysis in Duchenne and Becker muscular dystrophy
進行性肌營養不良患者視網膜眼電圖表型與臨床分型及基因型的關系
Determination of Phospholipids in Erythrocyte Membrane from Duchenne Muscular Dystrophy by High Performance Liquid Chromatography
肌營養不良癥患者紅細胞膜磷脂組成的高效液相色譜分析
Dystrophin detection by immunofluorescent technique for diagnosing muscular dystrophy
免疫熒光檢測抗肌萎縮蛋白診斷肌營養不良癥的臨床應用
Myoblast transfer treatment for Duchenne muscular dystrophy Cochrane Neuromuscular Disease Group
成肌細胞移植治療進行性肌營養不良
Analysis of short tandem repeat polymorphism in a female patient with Duchenne muscular dystrophy
非缺失型女性Duchenne型肌營養不良癥患者短串聯重復序列多態性分析
Misdiagnosed case analyses: Duchenne type muscular dystrophy was erroneously diagnosed as hepatitis
進行性肌營養不良誤診斷為病毒性肝炎的分析
A preliminary study of gene products encoded by disease genes of muscular dystrophy
肌營養不良癥致病基因編碼產物檢測的初步研究
Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy
肌營養不良癥患者肌肉中肌營養蛋白與神經元型一氧化氮合酶相互關系的研究
