Clinical study of concurrent transplantation of autologous peripheral blood stem cells and cord blood mesenchymal stem cells in patients with progressive muscular dystrophy 外周血和脐血干细胞联合移植治疗肌营养不良临床研究
Members will recall that the sun moved juvenile yellow figures Ge& it? 7-year-old when he was diagnosed with congenital progressive muscular dystrophy. 大家还记得感动人物&阳光少年黄舸吗?他7岁时,被确诊为先天性进行性肌营养不良。
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
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: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。
Ultrastructural Observation of Progressive Muscular Dystrophy 进行性肌营养不良症的超微结构观察
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
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
Duchenne muscular dystrophy ( DMD) is a fatal, genetic neuromuscular disorders that manifests as progressive muscle wasting. Although there has been enormous progress in the studies of the molecular mechanism of muscular dystrophy, there is still no cure. Duchenne型肌营养不良症(duchennemusculardystrophy,DMD)表现为进行性肌肉萎缩,是一种致死性、遗传性神经肌肉疾病。
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
Change of Nitric Oxide Synthase in Different Brain Regions in Rats during Cerebral Ischemia and Reperfusion Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy 大鼠脑缺血再灌流脑区一氧化氮合酶的变化肌营养不良症患者肌肉中肌营养蛋白与神经元型一氧化氮合酶相互关系的研究
Expressions of connective tissue growth factor and transforming growth factor-β 1 in progressive muscular dystrophy and their relationship with muscle fibrosis CTGF和TGF-β1在进行性肌营养不良中的表达及与肌肉纤维化的关系
The activity of serum CPK, LDH, GOT and GPT was determined in 49 case of progressive muscular dystrophy ( PMD). 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。
Objective The mechanism of the fibrosis in muscles with progressive muscular dystrophy is not clear. 目的进行性肌营养不良肌纤维化的病理机制不清。
CT Manifestations of Progressive Muscular Dystrophy Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy 进行性肌营养不良症的CT表现
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。
A Clinical Report of Progressive Muscular Dystrophy Treated with Water-Soluble Uridine Preparation 尿嘧啶核苷治疗9例进行性肌营养不良的临床观察
Methods The monoclonal antibody of dystrophin was used to analyse the muscle specimens from 107 cases of progressive muscular dystrophy by immunohistochemistry, and 13 cases of normal muscle were used as controls. 方法用抗dyshophin抗体对107例肌营养不良症患者肌组织标本行免疫组织化学分析。
A study on enzymology and morphology in progressive muscular dystrophy 进行性肌营养不良的酶学和形态学研究
Our data demonstrated that the pathogenesis of some types or subtypes of progressive muscular dystrophy is probably associated with the altered myostatin expression and the processing inhibition of myostatin protein. 结果提示,一些类型(亚型)的进行性肌营养不良可能与肌肉抑制素Myostatin基因表达异常、蛋白加工障碍有关。