肌营养不良症

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 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 ) .

面肩肱型肌营养不良症（FSHD）是一种进行肌肉疾病，多于30岁以前发病，面肌总有受累；然后是肩肿带肌，能后是盆带肌等的萎缩和力弱。

Facioscapulohumeral muscular dystrophy ( FSHD ) is a kind of progressive muscular disorder . It often occurs before 30 years old The face is initially involved , then the shoulder girdle , and finally the pelvic muscles Asymmetry of weakness is not unusual .

进行性肌营养不良症的CT表现

CT Manifestations of Progressive Muscular Dystrophy Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy

目的研究CKMM亚型用于肌营养不良症疗效判定的价值。

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

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

135例Duchenne型肌营养不良症DMD基因缺失分析

DMD gene defection analysis in 135 patients with Duchenne muscular dystrophy

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

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

Duchenne肌营养不良症高风险家系的产前基因诊断

Prenatal gene diagnosis in high danger families with Duchenne muscular dystrophy

X&连锁肌营养不良症的RFLP连锁分析

RFLP linkage analysis of X-linked muscular dystrophy

Duchenne型肌营养不良症心肌损害早期的治疗研究

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

高频超声对Duchenne型肌营养不良症的诊断价值

Value of high-frequency ultrasound in diagnosing Duchenne muscular dystrophy

Duchenne型肌营养不良症肌细胞膜异常的研究

The study of Membrane Abnormalities in Duchenne Muscular Dystrophy

Becker型肌营养不良症患者肌纤维组织化学特征的研究

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

Analysis of short tandem repeat polymorphism in a female patient with Duchenne muscular dystrophy

Duchenne型肌营养不良症的植入前遗传学诊断

Preimplantation Genetic Diagnosis for Duchenne Muscular Dystrophy

探讨体液免疫和细胞免疫在进行性肌营养不良症（PMD）发病过程中的作用。

Objective To study the effects of humoral and cellular immunity in pathologic progress in progressive muscular dystrophies ( PMD ) .

Duchenne型肌营养不良症的细胞治疗

Cell therapy for Duchenne muscular dystrophy

本文对49例进行性肌营养不良症（PMD）中的DMD、LG、FSH三型进行了血清CPK、LDH、GOT及GPT四种酶活性测定与分析。

The activity of serum CPK , LDH , GOT and GPT was determined in 49 case of progressive muscular dystrophy ( PMD ) .

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。

Objective To detect dystrophin gene deletion of Duchenne muscular dystrophy ( DMD ) and make DMD gene diagnosis .

目的检测假肥大肌营养不良症肌组织中肌营养不良蛋白（dystrophin）的表达。

Objective To detect dystrophin expressions in muscle tissues of the patients with Duchenne Becker muscular dystrophy .

作者等对一个Becker型肌营养不良症家系中的3名患者与3名递体进行了肌肉活组织检查。

Muscle biopsies of 3 patients and 3 carriers in a family with Becker type muscular dystrophy were performed .

目的探讨我国东北地区杜氏型肌营养不良症（DMD）及贝克型肌营养不良症（BMD）患者抗肌营养不良蛋白基因缺失类型分布与表型的关系，并用于产前基因诊断。

Objective To detect the distribution characteristics of dystrophin gene deletions in the northeastern of China and the relationship of severity with type of deletion .

目的观察Becker型肌营养不良症（BMD）患者病变肌纤维组织化学特征及其临床意义。

Objective To investigate the histochemical characteristics of muscle fiber in patients with Becker type muscular dystrophy ( BMD ) and its clinical significance .

CK-MM亚型用于肌营养不良症疗效判定的初步研究

Primary study of CK-MM used to determine the curative effect of muscular dystrophy

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。

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：对一个假肥大型进行性肌营养不良症（beckermusculardystro-phy，BMD）家族中的女性和胎儿进行携带者和产前基因诊断。

AIM : To perform gene diagnosis for female and fetal carriers as well as prenatal diagnosis in a family of Becker 's progressive muscular dystrophy ( BMD ) .

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 ) .

BglⅡ-BlnⅠ剂量检测方法在面肩肱型肌营养不良症1A基因诊断中的应用

Application of the Bgl ⅱ - Bln ⅰ dosage test to gene diagnosis of facioscapulohumeral muscular dystrophy 1A gene