muscular dystrophy

He had muscular dystrophy.

他患了肌肉萎缩症.

What is neuromuscular disease and muscular dystrophy?

什么是神经肌肉疾病和肌肉萎缩症?

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.

Prenatal gene diagnosis in high danger families with Duchenne muscular dystrophy

Duchenne肌营养不良症高风险家系的产前基因诊断

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.

Study of histochemical characteristics of muscle fiber in patients with Becker type muscular dystrophy

Becker型肌营养不良症患者肌纤维组织化学特征的研究

Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression

先天性肌营养不良的诊断及层黏连蛋白表达的意义

Clinical pathologic studies and genetic analysis of a female Duchenne muscular dystrophy family

女性假肥大型肌营养不良症家系的临床病理和基因分析

Detection of Duchenne Muscular Dystrophy Carrier by Fluorescence Quantitative Polymerase Chain Reaction

荧光定量PCR在缺失型DMD携带者检测中的应用

Objective To study the clinic and pathological features of 4 cases of lipid storage myopathy ( LSM) and differential diagnosis with Duchenne/ Becker muscular dystrophy 、 limb-girdle muscular dystrophies and polymyositis.

目的通过分析4例被误诊的脂质沉积性肌病的临床及病理特点，探讨脂质沉积性肌病被误诊的原因及与假肥大型肌营养不良、肢带型肌营养不良及多发性肌炎的鉴别诊断。

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.

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

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.

Clinical features and gene diagnosis of Duchenne/ Becker muscular dystrophy

假肥大型肌营养不良症40例临床特征与基因诊断

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.

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.

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.

A study on correlated gene of childhood Duchenne muscular dystrophy

杜氏肌营养不良患儿的相关基因研究

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.

Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation

脐血干细胞移植治疗假肥大型肌营养不良症

She was the poster child for muscular dystrophy.

她是海报上那个患肌肉萎缩的小孩.

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。

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.

Diagnosis of facioscapulohumeral muscular dystrophy using double enzyme digestion associated Southern blotting method

应用双酶切/Southern杂交方法诊断面肩肱型肌营养不良

Cell therapy for Duchenne muscular dystrophy

Duchenne型肌营养不良症的细胞治疗

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。

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

Study on the early treatment of cardiac injury caused by Duchenne muscular dystrophy

Duchenne型肌营养不良症心肌损害早期的治疗研究

A study on the gene deletions in the Chinese Duchenne muscular dystrophy patients

中国人杜氏肌营养不良症患者基因缺失的研究

Preimplantation Genetic Diagnosis for Duchenne Muscular Dystrophy

Duchenne型肌营养不良症的植入前遗传学诊断