Literature DB >> 3043217

EMG computerized analysis of localized fatigue in Duchenne muscular dystrophy.

M Frascarelli1, L Rocchi, I Feola.   

Abstract

EMG power spectra obtained during a sustained isometric contraction were analyzed in a group of 10 children affected by Duchenne muscular dystrophy (DMD) and compared with those obtained in a control group of 5 normal children. In myopathic subjects the isometric contraction caused an increase of the total power, a progressive increase of power of the lower frequencies, a decrease of that of the higher frequencies, and a shift downward of the median frequency. In normal children an increase of the total power without a significant median frequency shift was noted. The modifications observed in DMD children were explained by a decrement of the firing rate of the more damaged fast twitch motor units. This decrease was probably induced by a relative predominance of activity of the slow twitch motor units, which are less damaged by the pathological process.

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Year:  1988        PMID: 3043217     DOI: 10.1002/mus.880110712

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  10 in total

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Authors:  James G Tidball; Steven S Welc; Michelle Wehling-Henricks
Journal:  Compr Physiol       Date:  2018-09-14       Impact factor: 9.090

2.  Proteomic assessment of the acute phase of dystrophin deficiency in mdx mice.

Authors:  D Gardan-Salmon; J M Dixon; S M Lonergan; J T Selsby
Journal:  Eur J Appl Physiol       Date:  2011-03-16       Impact factor: 3.078

3.  Effects of in vivo injury on the neuromuscular junction in healthy and dystrophic muscles.

Authors:  Stephen J P Pratt; Sameer B Shah; Christopher W Ward; Mario P Inacio; Joseph P Stains; Richard M Lovering
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Review 4.  Nitric oxide synthase deficiency and the pathophysiology of muscular dystrophy.

Authors:  James G Tidball; Michelle Wehling-Henricks
Journal:  J Physiol       Date:  2014-09-05       Impact factor: 5.182

Review 5.  Alterations of neuromuscular junctions in Duchenne muscular dystrophy.

Authors:  Richard M Lovering; Shama R Iyer; Benjamin Edwards; Kay E Davies
Journal:  Neurosci Lett       Date:  2020-08-17       Impact factor: 3.046

6.  Loss of positive allosteric interactions between neuronal nitric oxide synthase and phosphofructokinase contributes to defects in glycolysis and increased fatigability in muscular dystrophy.

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Review 7.  The role of oxidative stress in skeletal muscle injury and regeneration: focus on antioxidant enzymes.

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Review 8.  Therapeutic strategies to address neuronal nitric oxide synthase deficiency and the loss of nitric oxide bioavailability in Duchenne Muscular Dystrophy.

Authors:  Cara A Timpani; Alan Hayes; Emma Rybalka
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9.  Surface EMG signals in very late-stage of Duchenne muscular dystrophy: a case study.

Authors:  Joan Lobo-Prat; Mariska M H P Janssen; Bart F J M Koopman; Arno H A Stienen; Imelda J M de Groot
Journal:  J Neuroeng Rehabil       Date:  2017-08-29       Impact factor: 4.262

Review 10.  The Neuromuscular Junction: Roles in Aging and Neuromuscular Disease.

Authors:  Shama R Iyer; Sameer B Shah; Richard M Lovering
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  10 in total

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