myotonic

1. 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。
2. People with myotonic dystrophy have prolonged muscle tensing ( myotonia) and are not able to relax certain muscles after use.
   患有强直性肌营养不良者骨骼肌收缩为持续性收缩（强直），特定肌肉在使用后不能放松。
3. The electrophysiological features in patients with myotonic syndrome The application of electrophysiologic detection in the microsurgical treatment for large acoustic neuromas
   肌强直疾病患者临床及神经电生理的检测分析电生理监测下切除大型听神经瘤临床研究
4. 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。
5. Aerobic training in patients with myotonic dystrophy type 1
   1型肌强直性营养不良患者的有氧训练
6. Clinical application of the molecular diagnostic technology for myotonic dystrophy
   强直性肌营养不良的分子诊断技术的临床应用研究
7. Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1
   青年肌强直性营养不良Ⅰ型患者的严重心律失常
8. Analysis of CTG repeat number of myotonic dystrophy ( DM) gene in DM patients and their family members
   强直性肌营养不良患者及家系成员基因的三核苷酸重复数检测
9. Myotonia and flaccid dysarthria in patients with adult onset myotonic dystrophy
   成年起病型强直性肌营养不良患者肌强直和弛缓型构音障碍
10. Comparison of CTG trinucleotide repeat numbers in blood and muscle tissues of myotonic dystrophy
    强直性肌营养不良的不同组织基因中CTG重复数比较研究
11. Clinical and Electrophysiological Study of Myotonic Dystrophy
    强直性肌营养不良的临床与电生理研究
12. Familial clustering of muscular and cardiac involvement in myotonic dystrophy type 1
    肌营养不良1型患者骨骼肌和心脏受累的家族聚集性
13. Clinical and Pathologic Reports of 3 Cases With Myotonic Muscular Dystrophy
    3例强直性肌营养不良的临床和病理报告
14. Cases of myotonic dystrophy occurring in the same family were reported.
    本文报导同一家族中患萎缩性肌强直症2例。
15. Fatigue and daytime sleepiness rating scales in myotonic dystrophy: A study of reliability
    一项强直性肌营养不良疲劳和日间嗜睡等级量表的可靠性研究
16. A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion
    一个非CTG非CCTG重复扩展型强直性肌营养不良家系
17. CTG repeat numbers of myotonic dystrophy gene in 91 cases of normal subjects in Shanghai area
    上海地区91名正常人强直性肌营养不良基因CTG重复数测定
18. Clinical and electrophysiological investigations were made in 20 members from 4 myotonic dystrophy ( MD) families.
    对患有萎缩性肌强直（MD）的4个家系的20名成员进行了临床及电生理调查研究。
19. Report of Seven Cases of Dystrophia Myotonica Clinical and Electrophysiological Features in 4 Families with Myotonic Dystrophy
    萎缩性肌强直三个家族七例报告萎缩性肌强直四家系的临床及电生理表现
20. Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions
    短CTG扩增患者的Ⅰ型肌强直性营养不良的临床特征
21. Falls and stumbles in myotonic dystrophy
    强直性肌营养不良患者的跌倒及绊倒
22. The results showed that the electrophysiological myotonic discharges were found in all patients, which were prominent in abductor pollicis brevis muscles.
    结果发现，全部患者均有电肌强直表现，其放电频率以拇短展肌最高。
23. 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
24. Comparative analysis of CTG repeat numbers and BAEP, TCD and ECG in patients with myotonic dystrophy
    强直性肌营养不良患者基因CTG重复数与BAEP、TCD、ECG对比分析
25. To summarize the clinical and pathological features of myotonic dystrophy and further the diagnosis of this disease.
    总结强直性肌营养不良的临床和病理特点，加深对本病的认识，提高诊断水平。
26. Sudden cardiac death in myotonic dystrophy type 2
    2型肌强直性营养不良的心源性猝死
27. Correlation between CTG trinucleotide repetition numbers of gene in myotonic dystrophy and electrocardiographic findings A clinical and pathological study of 3 cases of myotonic dystrophy
    强直性肌营养不良基因CTG数与心电图关系强直性肌营养不良的临床与肌肉病理研究
28. 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

adj

1. of or relating to or caused by myotonia