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.
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).
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.
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).
而她重返影坛是在本世纪初，扮演一个患肌营养不良症的妇女，这个角色让她跻身巨星行列。
She returned to movies in the early 2000s and played a woman with Muscular Dystrophy, which launched her superstardom.
目的对导致肌营养不良症的基因编码产物进行检测，从分子水平为临床诊断和分型提供依据。
Objective To provide a useful tool based on molecular level for clinical diagnosis and classification by detecting gene products encoded by disease genes of muscular dystrophy.
DMD是九种肌营养不良症的最常见类型，以缺少四肢等随意肌的肌营养不良蛋白为主要特征。
DMD is the most common of nine types of muscular dystrophy, which is characterized by a lack of the protein dystrophin in voluntary muscles, such as those in the arms and legs.
目的对面肩肱型肌营养不良症（FSHD）患者进行基因诊断并总结其临床特征，以提高FSHD的诊断水平。
Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.
目的为探讨假肥大型肌营养不良症（DMD）基因内含子的核苷酸序列特点与存在于内含子中的多个断裂点的关系。
Objective The purpose of the study was to investigate the relationship between the character of nucleic acids and the multiple breakpoints in the introns of DMD gene.
美国患adpkd的人数超过囊性纤维化、肌营养不良、血友病、唐氏综合症、镰刀细胞性贫血数种疾病加起来的患者。
In the U. S., the number of individuals affected by ADPKD is greater than the number affected by cystic fibrosis, muscular dystrophy, hemophilia, Down's syndrome, and sickle cell anemia combined.
美国患adpkd的人数超过囊性纤维化、肌营养不良、血友病、唐氏综合症、镰刀细胞性贫血数种疾病加起来的患者。
In the U. S., the number of individuals affected by ADPKD is greater than the number affected by cystic fibrosis, muscular dystrophy, hemophilia, Down's syndrome, and sickle cell anemia combined.
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