Gait abnormalities in type 1 myotonic muscular dystrophy: 3D motion analysis, energy cost and surface EMG

V. Tiffreau; C. Detrembleur; P. Van Den Bergh; A. Renders; V. Kinet; T. Lejeune

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Gait abnormalities in type 1 myotonic muscular dystrophy: 3D motion analysis, energy cost and surface EMG

机译：1型强直性肌营养不良症的步态异常：3D运动分析，能量消耗和表面肌电图

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Gait abnormalities in DM1 seem to be related to weakness and abnormal muscle activation of the calf. The implication of myotonia is suspected.

机译：DM1的步态异常似乎与小腿无力和肌肉异常激活有关。怀疑肌强直的影响。

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《Computer methods in biomechanics and biomedical engineering》 |2012年第1期|p.171-172|共2页
作者
V. Tiffreau; C. Detrembleur; P. Van Den Bergh; A. Renders; V. Kinet; T. Lejeune;
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作者单位

Service de MPR, Hopital Swynghedauw, CHRU de Lille, EA4488 'activitesphysiques, muscles, sante' Universite Lille Nord de France,Rue du Pr Verhaegue, 59037 Lille Cedex, France;

Rehabilitation and Physical Medicine Unit, Universite Catholique de Louvain,Avenue Mounier, 53 - UCL 5375, 1200 Brussels, Belgium;

Centre de Reference Neuromusculaire,Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium;

Centre de Reference Neuromusculaire,Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium;

Centre de Reference Neuromusculaire,Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium;

Rehabilitation and Physical Medicine Unit, Universite Catholique de Louvain,Avenue Mounier, 53 - UCL 5375, 1200 Brussels, Belgium;

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正文语种 eng
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关键词
myotonic dystrophy; gait analysis; kinematics; kinetics; EMG;

机译：强直性肌营养不良;步态分析运动学动力学;肌电图;

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1. Gait pattern in myotonic dystrophy (Steinert disease): A kinematic, kinetic and EMG evaluation using 3D gait analysis [J] . GalliM., CimolinV., CrugnolaV., Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2012,第1a2期

机译：强直性肌营养不良症（Steinert病）的步态模式：使用3D步态分析进行运动学，动力学和EMG评估
2. with myotonic muscular dystrophy type 1 but has not been evaluated in other myopathies. Methods: We measured total and free serum testosterone levels in 59 men with myotonic muscular dystrophy type 1 (N = 12), facioscapulohumeral muscular dystrophy (N = 11), dystrophinopathy (N = 12), metabolic myopathy (N = 7), and inclusion body myositis (N = 17) and compared these with the normal reference interval. Results: Thirty-two of the 59 (54%) participants had low total testosterone, 23 (39%) had low [J] . Anti-cancer agents in medicinal chemistry . 2009,第7期

机译：患有1型强直性肌营养不良症，但尚未在其他肌病中进行评估。方法：我们测量了59名患有强直性肌营养不良症1型（N = 12），面肩肱肱肌营养不良症（N = 11），肌营养不良症（N = 12），代谢性肌病（N = 7）和包涵体肌炎（N = 17），并将其与正常参考间隔进行比较。结果：59名参与者中的32名（54％）睾丸激素水平低，23名（39％）睾丸激素水平低
3. Chronic muscle stimulation improves muscle function and reverts the abnormal surface EMG pattern in Myotonic Dystrophy: a pilot study [J] . Carmelo Chisari, Federica Bertolucci, Stefania Dalise, Journal of NeuroEngineering Rehabilitation . 2013,第1期

机译：慢性肌肉刺激改善肌肉功能并恢复强直性肌营养不良症中异常的表面肌电图模式：一项初步研究
4. EMG-based Indicators of Muscular Co-Activation during Gait in Children with Duchenne Muscular Dystrophy [C] . M. Rinaldi, M. Petrarca, A. Romano, Annual International Conference of the IEEE Engineering in Medicine and Biology Society . 2019

机译：基于肌电图的杜兴氏肌营养不良症儿童步态中肌肉共激活的指标
5. Professional and lay facilitator's perceptions of roles, goals, and strategies to promote social support and self-management in face-to-face support groups for adults with multiple sclerosis and myotonic muscular dystrophy. [D] . Krongold, Leslie. 2010

机译：专业人士和外行促进者对角色，目标和策略的认知，以促进面对多发性硬化症和强直性肌营养不良症的成年人面对面的支持小组中的社会支持和自我管理。
6. Myocardial fibrosis by late gadolinium enhancement cardiovascular magnetic resonance in myotonic muscular dystrophy type 1: highly prevalent but not associated with surface conduction abnormality [O] . Andrea Cardona, William D. Arnold, John T. Kissel, 2019

机译：晚期g引起的心肌纤维化增强了1型强直性肌营养不良症的心血管磁共振作用：高度普遍但与表面传导异常无关
7. Chronic muscle stimulation improves muscle function and reverts the abnormal surface EMG pattern in Myotonic Dystrophy: a pilot study [O] . Carmelo Chisari, Federica Bertolucci, Stefania Dalise, 2013

机译：慢性肌肉刺激改善肌肉功能并恢复强直性肌营养不良症中异常的表面肌电图模式：一项初步研究
8. Surface EMG and Motor Control of the Upper Extremity in Muscular Dystrophy: A Pilot Study. [R] . Bowen, R. C., Seliktar, R., Rahman, T., 2001

机译：肌肉萎缩症上肢的表面肌电图和运动控制：一项初步研究。

Gait abnormalities in type 1 myotonic muscular dystrophy: 3D motion analysis, energy cost and surface EMG

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