dystrophy

Diagnostic value of serum creatine kinase and its isoenzyme MB determination in progressive muscular dystrophy and motor neuron disease

进行性肌营养不良症及运动神经元疾病的血清CK及其同工酶MB测定的诊断意义

Background: Duchenne muscular dystrophy is characterized by progressive cardiac dysfunction and myocardial fibrosis late process.

背景: Duchenne型 肌营养不良(DMD) 以进展性心功能不全及晚期心肌纤维化为特征.

Diseases like multiple sclerosis, muscular dystrophy or polio can leave people disabled.

像多发性硬化症 、 肌肉萎缩症或小儿麻痹症等疾病会使人残疾.

Study on characteristics of gene structure and gene diagnosis of facioscapulohumeral muscular dystrophy using pulse field gel electrophoresis

应用脉冲场电泳技术研究面肩肱型肌营养不良症的基因突变特征及进行基因诊断

These are genetic disorders that only affect males normally. They are things like muscular dystrophy and haemophilia

这些遗传病通常只发生在男性身上，如肌肉萎缩、血友病等。

Neurasthenia, neurasthenic syndrome, peripheral neuropathy, etc. amyotrophy, myasthenia, progressive muscular dystrophy.

神经衰弱 、 神经衰弱综合症 、 周围神经病等.肌萎缩 、 肌无力 、 进行性营养不良.

Objective To investigate the significance of CK MM isoforms to determine the curative effect of muscular dystrophy.

目的研究CK MM亚型用于肌营养不良症疗效判定的价值。

He had muscular dystrophy.

他患了肌肉萎缩症.

A clinical and ultrasounic examination was made on 120 sites of voluntary muscle from 29 cases with neuromuscular diseases, including varied muscular dystrophy, polymyositis, diversified neuro-genic myopathy and DMD possible carrier.

对29例神经肌肉疾病（包括多种肌营养不良，多发性肌炎，多种神经原性肌肉病变与DMD可能递体）的120处随意肌进行了临床与超声检查。

Objective: To identify the deletions in Duchenne/ Becker muscular dystrophy ( DMD/ BMD) by using fluorescence in situ hybridization ( FISH).

目的：应用荧光原位杂交（FISH）筛查技术检测假性肥大型肌营养不良症（DMD/BMD）缺失型携带者。

Objective: To investigate the pulmonary function characteristics and rehabilitation strategy for Becker muscular dystrophy ( BMD). The Psychological Condition of the Addicts and Healing Countermeasure.

目的：探讨良性假肥大型肌营养不良症（BMD）患者的肺功能表现特点与康复对策。

Gene Mutation Analysis of Duchenne Muscular Dystrophy and Tuberous Sclerosis Complex

杜氏肌营养不良症和结节性硬化症的基因突变分析

Clinical for muscular dystrophy, myasthenia gravis, muscular dystrophy, polymyositis, motor neuron disease, as atrophy disease syringomyelia.

临床用于肌肉萎缩 、 重症肌无力 、 肌营养不良 、 肌炎 、 运动神经元病 、 脊髓空洞症等痿症.

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 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.

Objective To evaluate the effect of microwave combined with Meibao burn fire plaster on vulva dystrophy.

目的观察微波照射联合美宝烧伤湿润膏治疗外阴营养不良的临床疗效.

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.

She was the poster child for muscular dystrophy.

她是海报上那个患肌肉萎缩的小孩.

These are genetic disorders that only affect males normally. They are things like muscular dystrophy and haemophilia.

这些遗传病通常只发生在男性身上，如肌肉萎缩、血友病等。

What is neuromuscular disease and muscular dystrophy?

什么是神经肌肉疾病和肌肉萎缩症?

DMD gene defection analysis in 135 patients with Duchenne muscular dystrophy

135例Duchenne型肌营养不良症DMD基因缺失分析

Establishment of Pulsed Field Gel Electrophoresis System and Study on the Gene Structure of Facioscapulohumeral Muscular Dystrophy in Chinese Population

脉冲电场凝胶电泳技术体系的建立与中国人面肩肱型肌营养不良症的基因分析

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.

Aim : To summarize the pathological characteristics of myotonic dystrophy ( DM ).

目的: 总结强直性肌营养不良 ( DM ) 的肌肉病理特点.

Objective To investigate the effect of bone marrow stem cell transplantation ( BMT) on the diaphragm muscles of mdx mice, a mouse model of Duchenne muscular dystrophy ( DMD).

目的探讨骨髓干细胞移植对假肥大型肌营养不良症（DMD）模型鼠-mdx鼠膈肌的治疗效果。

Objective To observe CT findings of progressive muscular dystrophy ( PMD) and to evaluate the diagnostic value of CT.

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。

In fleck corneal dystrophy, the lesion only involved stroma, epithelium and endothelium levels were normal.

斑点状角膜营养不良病变仅累及基质层, 而角膜上皮层及内皮层正常.

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.

Myotonic dystrophy is a degenerative disease characterized by progressive muscle wasting and weakness.

强直性肌营养不良症是一种退化性疾病,其症状是渐进性肌肉消瘦及虚弱.

Objective : To study the new therapy of vulval dystrophy and its efficacy and security.

目的: 探索外阴营养不良新的治疗方法及其有效性和安全性.