进行性肌营养不良症
- 网络Progressive muscular dystrophy;Pmd;DMD;progressive myodystrophy
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体液细胞免疫在进行性肌营养不良症发病过程中的作用
Effects of humoral and cellular immunity in pathologic progress in PMD by immunohistochemistry
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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
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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 .
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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
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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 ) .
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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 ) .
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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 ) .
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目的:杜氏进行性肌营养不良症(duchennemusculardystrophy,DMD)是一种有严重危害的X染色体隐性遗传病,在各类遗传病中,杜氏进行性肌营养不良症是发病率最高的疾病之一。
Purpose : Duchenne muscular dystrophy ( DMD ) is a kind of serious harmed x chromatin-linked recessive inherited disease , in all kinds of hereditary diseases , DMD is one of disease which have the highest incidence rate .
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假肥大型进行性肌营养不良症患儿髋、膝运动功能分析
An analysis of motor function of children with Duchenne muscular
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进行性肌营养不良症基因诊断及家系分析
Gene diagnosis and pedigree analysis in families of Duchenne and Becker muscular dystrophy
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进行性肌营养不良症的超微结构观察
Ultrastructural Observation of Progressive Muscular Dystrophy
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目的针药综合治疗进行性肌营养不良症的临床观察。
Objective The clinical observation of treatment with acupuncture and herbs for muscular pseudohypertrophy and progressive myodystrophy .
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目的在假肥大型进行性肌营养不良症家系中进行基因诊断与遗传咨询。
Objective Gene diagnosis and pedigree analysis were carried out in families of Duchenne and Becker muscular dystrophy ( DMD and BMD ) in order to determine haplotypes in the patients , carriers and normal offspring .