肌强直

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

Myotonia and flaccid dysarthria in patients with adult onset myotonic dystrophy

肌强直：随意肌收缩后松弛困难的一种肌肉疾。

Myotonia : disorder causing difficulty relaxing contracted voluntary muscles .

获得性神经性肌强直自发放电的起源：一项巨大EMG研究

The origin of spontaneous discharges in acquired neuromyotonia . A Macro EMG study

结果伴抑郁PD患者29例，占41.4%以运动迟缓和肌强直为主；

Results There were 29 ( 41.4 % ) patients with PD had depression . They mainly show movement retardation and paramyotonus ;

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。

Clinical and electrophysiological investigations were made in 20 members from 4 myotonic dystrophy ( MD ) families .

帕金森病（Parkinson'SDisease，PD）是一种老年人常见的慢性进展性运动障碍性疾病，患者可出现静止性震颤、肌强直、运动迟缓和姿势反射障碍等。

Parkinson 's disease ( PD ) is a common chronic progressive neurodegenerative disorder in elder people ; it is characterized by resting tremor , rigidity , bradykinesia and postural instability .

灵芝对2,4-二氯苯氧乙酸（2,4-D）引起的实验性肌强直症小鼠高血清醛缩酶的影响

The effect of ganodermas on elevated serum aldolase levels induced by 2,4-dichlorophen-oxyacetic acid ( 2,4-d ) in mice

神经性肌强直和边缘性脑炎患者血清中成熟的Shaker型K~+通道：与临床表现特异相关的亚单位

Neuromyotonia and limbic encephalitis sera target mature Shaker-type K ~ + channels : Subunit specificity correlates with clinical manifestations

帕金森病（Parkinson'SDisease，PD）是一中老年人常见的慢性进行性神经变性疾病，主要临床表现为震颤、运动减少、肌强直和姿势障碍等。

Parkinson 's disease ( PD ) is a chronic progressive neurodegenerative disorder among middle age and old-age persons . PD 's cardinal manifestations are tremor , rigidity , bradykinesia and postural instability et al .

短CTG扩增患者的Ⅰ型肌强直性营养不良的临床特征

Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions

萎缩性肌强直（MYD）患者红细胞膜生物物理特性的研究

Study on biophysical characteristics of erythrocytes membrane in myd

上述改变可能与肺癌有关，提示患者神经系统IgG介导的自身免疫异常在神经性肌强直的发病机理中起重要作用。

Conclusion The presence of oligoclonal bands and increased concentration of IgG in her spinal fluid suggests that a IgG antibodies mediated autoimmunity may play an important role in this patient 's pathogenesis of acquired neuromyotonia and Lambert-Eaton myasthenic syndrome associated with lung cancer .

用透镜测量人眼的屈光度和视力眼神经性肌强直

Determination of the eye dioptric strenght and vision by using lenses

眼神经性肌强直正交函数法测定新福林滴眼液

Determination of phenylephrine hydrochloride eye drops by orthogonal function spectrophotometric method

通过检查单眼眨眼诊断前庭平衡失调眼神经性肌强直

Diagnosis of vestibular imbalance in the blink of an eye

观察了该滴眼液的稳定性和刺激性。双氯芬酸胆碱滴眼剂的稳定性和刺激性眼神经性肌强直

Study on the trill and stability of diclofenac acid-choline eyedrops

本文报导同一家族中患萎缩性肌强直症2例。

Cases of myotonic dystrophy occurring in the same family were reported .

眼神经性肌强直长期配戴义眼患者眼睑畸形的矫正

Plastic surgeries for lid abnormity due to long-term wearing of artificial eye

肌强直明显而震颤相对较轻；

The rigidity was more seriously than the tremor .

临床表现为肌萎缩，肌强直，并伴代谢障碍。

The clinical manifestations were muscular atrophy and myotone accompanied by metabolic dysfunction .

放疗后发生的咬肌神经性肌强直（法国）

Post-irradiation neuromyotonia of the masseter muscle ( Fren )

1型肌强直性营养不良患者的有氧训练

Aerobic training in patients with myotonic dystrophy type 1

增加刺激频率不影响大鼠萎缩比目鱼肌强直收缩疲劳性

No influence of increased frequency on fatigability of tetanic contraction in rat atrophic soleus

2型肌强直性营养不良的心源性猝死

Sudden cardiac death in myotonic dystrophy type 2

肌强直患者鼻音功能亢进的个案分析

Analysis of nasal hyperpituitarism induced by myotonia

实时眼动仪系统眼神经性肌强直

A Real Time Eye Movement Measuring System

糖尿病视网膜病眼内后部玻璃体切割术眼神经性肌强直

Posterior vitrectomy in eyes with diabetic retinopathy

人眼模型及其运动控制眼神经性肌强直

Model of Eyes and Movement Control

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

Report of Seven Cases of Dystrophia Myotonica Clinical and Electrophysiological Features in 4 Families with Myotonic Dystrophy

显效为震颤和肌强直消失，姿势异常消失，渐停止服用多巴胺制剂等药物；

Excellence as tremor , myotonia and postural instability disappeared , and patients gradually stopped taking dopamine preparation ;