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.
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.
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).
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).
目的：调查假肥大型肌营养不良（DMD）患者家系中女性携带者生育情况，探讨影响DMD家系生育的因素。
Objective:To investigate the fertility condition of Female Carriers from the families of Duchenne Muscular Dystrophy( DMD). To explore factors influencing fertility condition of DMD families.
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.
研究假肥大型肌营养不良(DMD)病人肌酸激酶同工酶(CK - MB)及其亚型的变化，为早期诊断和判定病情提供依据。
To study the changes of creatine kinase isoenzyme (CK-MB) and its isoforms in patient with DMD for the purpose of early diagnosis and evaluation, a discontinuous buffer system was used.
研究假肥大型肌营养不良(DMD)病人肌酸激酶同工酶(CK - MB)及其亚型的变化，为早期诊断和判定病情提供依据。
To study the changes of creatine kinase isoenzyme (CK-MB) and its isoforms in patient with DMD for the purpose of early diagnosis and evaluation, a discontinuous buffer system was used.
应用推荐