muscular dystrophy

Conclusion Repeat sequence polymorphism as well as gene dosage analysis can potentially be used in carrier detection in the deleted families of Duchenne and Becker muscular dystrophy .

结论重复顺序多态性与基因剂量分析结合可有效地检测缺失型迪谢内和贝克肌营养不良的女性携带者。

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。

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。

Clinical analysis on 16 cases of children progressive muscular dystrophy

儿童进行性肌营养不良16例临床分析

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。

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

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

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

Expression of connective tissue growth factor in progressive muscular dystrophy

结缔组织生长因子在进行性肌营养不良中的表达

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

Preliminary study of molecular deletion on X linked muscular dystrophy

X-连锁肌营养不良症分子缺失的初步研究

Pulmonary Function Characteristics and Rehabilitation Strategy for Becker Muscular Dystrophy

良性假肥大型肌营养不良症患者肺功能的表现特点与康复对策

Genes and Their Functional Mechanisms in the Pathogenesis of Muscular Dystrophy

肌营养不良致病基因及发病机制

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

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

There is no specific treatment for any of the forms of muscular dystrophy .

有没有具体的治疗任何形式的肌肉萎缩症。

The analysis of clinical and pathological feature in oculopharyngeal muscular dystrophy

眼、咽型肌营养不良的临床及病理特点分析

Altered Expression of Myostatin Gene in the Progressive Muscular Dystrophy Patients

进行性肌营养不良患者Myostatin基因的表达分析

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

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

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

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

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

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

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

Allogeneic umbilical cord blood stem cell transplantation in Duchenne muscular dystrophy

异基因脐带血干细胞移植治疗假肥大型肌营养不良症一例

Clinical and Pathologic Reports of 3 Cases With Myotonic Muscular Dystrophy

3例强直性肌营养不良的临床和病理报告

Clinical application of prenatal gene diagnosis of Duchenne and Becker muscular dystrophy

假肥大型肌营养不良症产前基因诊断的临床应用

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。

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