1型强直性肌营养不良症的步态异常：三维运动分析、能量消耗及表面肌电图 - Suppr

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

作者信息

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

机构信息

Service de MPR, Hopital Swynghedauw, CHRU de Lille, EA 4488 activités physiques, muscles, santé, Université Lille Nord de France, Rue du Pr Verhaegue, 59037, Lille Cedex, France.

出版信息

Comput Methods Biomech Biomed Engin. 2012;15 Suppl 1:171-2. doi: 10.1080/10255842.2012.713709.

DOI:10.1080/10255842.2012.713709

PMID:23009467

Abstract

摘要

相似文献

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

Comput Methods Biomech Biomed Engin. 2012;15 Suppl 1:171-2. doi: 10.1080/10255842.2012.713709.

Gait pattern in myotonic dystrophy (Steinert disease): a kinematic, kinetic and EMG evaluation using 3D gait analysis.

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[Diaphragmatic EMG using transesophageal electrodes in a myotonic dystrophy patient].

Nihon Kyobu Shikkan Gakkai Zasshi. 1988 Nov;26(11):1150-3.

Conventional electromyography in myotonic dystrophy.

Riv Patol Nerv Ment. 1976 Sep-Oct;97(5):263-76.

[Electromyographic studies on myotonic dystrophy].

Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1991 Oct;24(5):297-9, 319.

Pulmonary function and electromyographic study of respiratory muscles in myotonic dystrophy.

Muscle Nerve. 1985 Sep;8(7):586-94. doi: 10.1002/mus.880080708.

Orthopaedic manifestations of congenital myotonic dystrophy during childhood and adolescence.

J Pediatr Orthop. 2009 Mar;29(2):208-13. doi: 10.1097/BPO.0b013e3181982bf6.

Absent, unrecognized, and minimal myotonic discharges in myotonic dystrophy type 2.

Muscle Nerve. 2010 Jun;41(6):758-62. doi: 10.1002/mus.21615.

[Myotonic muscular dystrophy (clinical and electromyographic studies of 21 cases)].

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1984 Aug;6(4):256-60.

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Functional Ambulation Profile (FAP) Score as a Potential Marker of Gait Analysis in Myotonic Dystrophy Type 1.

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Electromechanical delays during a fatiguing exercise and recovery in patients with myotonic dystrophy type 1.

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

作者信息

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

机构信息

Service de MPR, Hopital Swynghedauw, CHRU de Lille, EA 4488 activités physiques, muscles, santé, Université Lille Nord de France, Rue du Pr Verhaegue, 59037, Lille Cedex, France.

出版信息

Comput Methods Biomech Biomed Engin. 2012;15 Suppl 1:171-2. doi: 10.1080/10255842.2012.713709.

DOI:10.1080/10255842.2012.713709

PMID:23009467

Abstract

摘要

相似文献

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

Comput Methods Biomech Biomed Engin. 2012;15 Suppl 1:171-2. doi: 10.1080/10255842.2012.713709.

Gait pattern in myotonic dystrophy (Steinert disease): a kinematic, kinetic and EMG evaluation using 3D gait analysis.

J Neurol Sci. 2012 Mar 15;314(1-2):83-7. doi: 10.1016/j.jns.2011.10.026. Epub 2011 Nov 25.

Fluoxetine blocks myotonic runs and reverts abnormal surface electromyogram pattern in patients with myotonic dystrophy type 1.

Clin Neuropharmacol. 2009 Nov-Dec;32(6):330-4. doi: 10.1097/WNF.0b013e3181ae5546.

[Diaphragmatic EMG using transesophageal electrodes in a myotonic dystrophy patient].

Nihon Kyobu Shikkan Gakkai Zasshi. 1988 Nov;26(11):1150-3.

Conventional electromyography in myotonic dystrophy.

Riv Patol Nerv Ment. 1976 Sep-Oct;97(5):263-76.

[Electromyographic studies on myotonic dystrophy].

Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1991 Oct;24(5):297-9, 319.

Pulmonary function and electromyographic study of respiratory muscles in myotonic dystrophy.

Muscle Nerve. 1985 Sep;8(7):586-94. doi: 10.1002/mus.880080708.

Orthopaedic manifestations of congenital myotonic dystrophy during childhood and adolescence.

J Pediatr Orthop. 2009 Mar;29(2):208-13. doi: 10.1097/BPO.0b013e3181982bf6.

Absent, unrecognized, and minimal myotonic discharges in myotonic dystrophy type 2.

Muscle Nerve. 2010 Jun;41(6):758-62. doi: 10.1002/mus.21615.

[Myotonic muscular dystrophy (clinical and electromyographic studies of 21 cases)].

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1984 Aug;6(4):256-60.

引用本文的文献

A multi-sensor approach to improve interpretability of the 6-min walk test as an outcome in muscular dystrophies: an observational study.

Brain Commun. 2025 Jun 5;7(3):fcaf205. doi: 10.1093/braincomms/fcaf205. eCollection 2025.

Functional Ambulation Profile (FAP) Score as a Potential Marker of Gait Analysis in Myotonic Dystrophy Type 1.

Front Neurol. 2020 May 19;11:392. doi: 10.3389/fneur.2020.00392. eCollection 2020.

Paving the way for a better understanding of the pathophysiology of gait impairment in myotonic dystrophy: a pilot study focusing on muscle networks.

J Neuroeng Rehabil. 2019 Sep 18;16(1):116. doi: 10.1186/s12984-019-0590-0.

Electromechanical delays during a fatiguing exercise and recovery in patients with myotonic dystrophy type 1.

Eur J Appl Physiol. 2017 Mar;117(3):551-566. doi: 10.1007/s00421-017-3558-4. Epub 2017 Feb 14.

Gait characteristics in a canine model of X-linked myotubular myopathy.

J Neurol Sci. 2014 Nov 15;346(1-2):221-6. doi: 10.1016/j.jns.2014.08.032. Epub 2014 Aug 29.

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

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

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