1.People with myotonic dystrophy have prolonged muscle tensing (myotonia) and are not able to relax certain muscles after use.
强直性肌营养不良病患具长期肌肉拉紧（肌强直）和在使用后无法放松某些肌肉。
2.A disorder due to a similar molecular basis, myotonic dystrophy 1 (DM1), is known to have white matter hyperintensities on cranial MRI.
另一种有类似分子病理学基础的疾病：萎缩性肌强直（DM1）患者的核磁共振成像也有白质高信号。
3.We report a laboratory-confirmed pediatric case of congenital myotonic dystrophy (CMD) in Taiwan.
我们报告一例台湾地区之先天型肌强直失状症的儿童个案。
4.Objective To summarize the clinical characteristics of myotonic dystrophy (DM).
目的总结强直性肌营养不良症（DM）的临床特点。
5.Aim: To summarize the pathological characteristics of myotonic dystrophy (DM).
目的：总结强直性肌营养不良（DM）的肌肉病理特点。
6.Quick movements cause muscle stiffening. There is also a myotonic form of muscular dystrophy.
快速运动会引起肌强直，肌营养不良是另一种肌强直类型。
7.Over time it became apparent that a central player in myotonic dystrophy was RNA, a versatile molecule that is very similar to DNA.
随着时间推移，很明显RNA在强直性肌营养不良中起了核心作用，RNA是一种类似于DNA普遍存在的分子。
8.Objective To study the clinical and pathology features of myotonic dystrophy (DM).
目的探讨强直性肌营养不良症（DM）的临床及肌肉病理学的特点。
9.Clinical and Electrophysiological Study of Myotonic Dystrophy
强直性肌营养不良的临床与电生理研究
10.DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai
上海松江一个强直性肌营养不良家系DNA检测