myotonic

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。

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。

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。

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。

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。

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。

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。

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。

Clinical and Electrophysiological Study of Myotonic Dystrophy

强直性肌营养不良的临床与电生理研究

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

Phasic study of the new susceptible gene locus of myotonic dystrophy

强直性肌营养不良症致病新位点的阶段性研究

Study on muscular pathological characteristics in myotonic dystrophy

强直性肌营养不良症患者肌肉病理学特点研究

Clinical characteristics of myotonic dystrophy

强直性肌营养不良症的临床特点

Cataract and myotonic dystrophy: the role of molecular diagnosis

强直性肌营养不良与白内障的分子诊断关系

Myotonic dystrophy with peripheral damage

伴有周围神经损害的强直性肌营养不良

CTG repeat numbers and anticipation in Myotonic Dystrophy

CTG重复数与强直性肌营养不良的遗传早现现象

Facial emotion recognition in myotonic dystrophy type 1 correlates with CTG repeat expansion

1型强直性肌营养不良患者的面部表情识别与CTG的重复扩增相关

C-MMD Congenital myotonic muscular dystrophy

先天肌强直性营养不良

Falls and stumbles in myotonic dystrophy

强直性肌营养不良患者的跌倒及绊倒