这个可怜的家伙，一心想着奇妙的世界，却患了金币消化不良症。
The poor fellow, with his mind on the Field of Wonders, was suffering from a gold-piece indigestion.
这样的话，他们可能会的营养不良症。
患有慢性消化不良症的病人不能多吃。
Patients suffering from chronic indigestion cannot eat more than enough.
橙色丝带：代表对营养不良症的关注。
目前没有任何形式的治愈肌肉营养不良症。
There's currently no cure for any form of muscular dystrophy.
营养不良症不能在一种控制的状态下进行研究。
The effects of a dietary deficiency cannot be studied in a controlled way.
我正患消化不良症。
他患消化不良症。
目的针药综合治疗进行性肌营养不良症的临床观察。
Objective The clinical observation of treatment with acupuncture and herbs for muscular pseudohypertrophy and progressive myodystrophy.
一项最近的调查显示50%的儿童患有营养不良症。
A recent study has revealed that the 50% of the childrens are suffering from the malnutrition.
目的对贝克氏型肌营养不良症女性患者的家系追踪研究。
Objective To investigate the genealogical tree of women with Becker muscular dystrophy (BMD).
他脑部和颈椎的核磁共振成像证实了他患有髓鞘功能不良症。
An MRI of his brain and cervical spine has confirmed the presence of dysmyelination.
强直性肌营养不良症为一种少见的多系统受累的遗传性疾病。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
他最近利用此法治疗动物的杜兴氏肌营养不良症，结果很有效。
He recently used it to treat animals with Duchenne muscular dystrophy, and the results have been promising.
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。
Blood samples are examined for mutations in some of the genes that cause different 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。
Research into gene therapy may eventually provide treatment to stop the progression of some types of muscular dystrophy.
目的研究进行性肌营养不良症（PMD）的CT表现及CT在诊断中的价值。
Objective To observe CT findings of progressive muscular dystrophy(PMD)and to evaluate the diagnostic value of CT.
方法回顾性分析本院40年来收治的82例先天性肠旋转不良症的临床资料。
Method the clinical data of 82 patients with congenital malrotation of intestine, admit ted and treated during the present 40 years, were analysed retrospectively.
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。
Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
目的探讨面肩肱型肌营养不良症（FSHD）1A的基因型与临床表型之间的相关关系。
Objective To explore the genotype-phenotype correlation of facioscapulohumeral muscular dystrophy (FSHD) 1A gene.
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。
ABSTRACT: Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
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 returned to movies in the early 2000s and played a woman with Muscular Dystrophy, which launched her superstardom.
目的对导致肌营养不良症的基因编码产物进行检测，从分子水平为临床诊断和分型提供依据。
Objective To provide a useful tool based on molecular level for clinical diagnosis and classification by detecting gene products encoded by disease genes of muscular dystrophy.
DMD是九种肌营养不良症的最常见类型，以缺少四肢等随意肌的肌营养不良蛋白为主要特征。
DMD is the most common of nine types of muscular dystrophy, which is characterized by a lack of the protein dystrophin in voluntary muscles, such as those in the arms and legs.
婴儿、儿童、孕妇和哺乳期妇女、病人以及老人非常容易患上营养不良症，他们都有特殊的需要。
Infants, children, pregnant and lactating women, the sick, and the elderly are very vulnerable to malnutrition and have special needs.
研究人员强调指出， 80 ％的受试者暴露于上述污染工作制定慢性营养不良症和过敏影响鼻，咽喉。
The investigators emphasize that 80% of the subjects exposed to the above pollution at their jobs develop chronic dystrophy and allergy affecting nose, pharynx and larynx.
目的对面肩肱型肌营养不良症（FSHD）患者进行基因诊断并总结其临床特征，以提高FSHD的诊断水平。
Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.
目的对面肩肱型肌营养不良症（FSHD）患者进行基因诊断并总结其临床特征，以提高FSHD的诊断水平。
Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.
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