需要用针灸和草药治疗肌肉假性肥大和进行性肌营养不良的临床观察。
The clinical observation of treatment with acupuncture and herbs for muscular pseudohypertrophy and progressive myodystrophy are required.
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.
本发明涉及一种治疗杜兴氏肌营养不良疾病的药物。
The present invention is one medicine for treating Duchenne muscular dystrophy.
目的对贝克氏型肌营养不良症女性患者的家系追踪研究。
Objective To investigate the genealogical tree of women with Becker muscular dystrophy (BMD).
目的：总结强直性肌营养不良(DM)的肌肉病理特点。
Aim: to summarize the pathological characteristics of myotonic dystrophy (DM).
快速运动会引起肌强直，肌营养不良是另一种肌强直类型。
Quick movements cause muscle stiffening. There is also a myotonic form of muscular dystrophy.
我今年16岁，住在加拿大安大略省，患有先天性肌营养不良。
I am 16 years old and live in Ontario, Canada and have congenital muscular dystrophy.
强直性肌营养不良症为一种少见的多系统受累的遗传性疾病。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
他最近利用此法治疗动物的杜兴氏肌营养不良症，结果很有效。
He recently used it to treat animals with Duchenne muscular dystrophy, and the results have been promising.
结果肌营养不良蛋白聚糖复合体表达于RT4细胞的细胞膜上。
Results The dystroglycan complex was observed expressing on RT4 cell membrane and molecular weight was tested.
回顾性分析24例强直性肌营养不良患者的临床和病理资料。
The clinical and pathological characteristics of 24 DM cases were analyzed retrospectively.
结论假肥大型肌营养不良患者骨骼肌纤维再生与年龄有相关性。
But quantities was larger. Conclusion The capacity of muscle fibers regeneration in pseudohypertrophic muscular dystrophy was correlated with age.
观察一个肢带型肌营养不良伴心肌损害家系患者的临床病理特点。
Objective To observe the clinical and pathological characteristics of a 1imb-girdle muscular dystrophy and myocardial impairment family.
在肌营养不良蛋白基因，在人类基因大多数，这种遗传信息不连续的。
In the dystrophin gene, and in most of human genes, this genetic information is not contiguous.
多数患进行性假肥大性肌营养不良的儿童可以活到十几岁或20几岁。
Most children with Duchenne muscular dystrophy die in their late teens or early 20s.
肌营养不良卵白基因位于人类X染色体，携带基因突变的母亲会遗传给婴儿。
The dystrophin gene is found on the X chromosome and passed on to children through a mother who is a carrier.
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.
肌营养不良是30种遗传性疾病的一种，以骨骼肌进展性无力和变性为特点。
Muscular dystrophy is a group of more than 30 genetic diseases, characterized by progressive weakness and deterioration of skeletal muscles.
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。
Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
目的观察大鼠神经鞘瘤细胞(rt4)中肌营养不良蛋白聚糖复合物的表达状况。
Objective To examine the expression of dystroglycan complex in the membrane of rat's schwannoma cell (RT4).
重要的是要注意，不过，在不同的肌营养不良基因突变可能需要不同的寡核苷酸药物。
It is important to note, however, that different mutations in the dystrophin gene could require different oligonucleotide drugs.
目的通过对进行性肌营养不良的临床综合分析，探讨该病的早期诊断方法，减少误诊。
Objective To make a correct diagnosis in the early stage and avoid misdiagnosis, we analysed clinical data of patients with Duchenne type muscular dystrophy(DMD).
像色盲，肌营养不良等X连锁的疾病一样，由遗传突变导致的不育可以从母亲传给儿子。
Like other X-linked disorders such as color blindness and muscular dystrophy, genetic mutation causing a son's infertility could be passed from his mother.
研究者建立了治疗强直性肌营养不良的概念，相信下一步开发一种有效的药物应该很快。
However, having established a general concept of what a treatment for myotonic dystrophy may look like, researchers believe that the next steps in developing an effective drug should go faster.
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.
的确，用曲古抑菌素治疗数月的肌营养不良鼠与未经治疗的鼠相比显示正常的组织结构。
Indeed, muscles examined from dystrophic mice treated with Trichostatin a for three months displayed normal tissue architecture, as compared to the muscles examined from untreated, dystrophic mice.
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).
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).
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