Literature DB >> 3550413

Strength evaluation in neuromuscular disease.

J D Cook, D S Glass.   

Abstract

Strength evaluation in neuromuscle disease is necessary to track the natural history of the disease, to understand its pathophysiology, to determine the efficacy of treatment, and, most importantly, to evaluate an experimental treatment regimen. This article describes the physiology of muscle activity, discusses fatigue, examines various testing methods, and suggests appropriate measurements to assess the neuromuscular patient's strength and endurance in a variety of clinical settings. The minimal amount of equipment necessary to follow patients with NMD is a stop watch, a goniometer, a hand-held dynamometer, a hand-grasp dynamometer, and a creative mind.

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Year:  1987        PMID: 3550413

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  6 in total

1.  Hand-held myometry: reference values.

Authors:  R J van der Ploeg; V Fidler; H J Oosterhuis
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-03       Impact factor: 10.154

2.  Application of ultrasound elastography in the evaluation of muscle strength in a healthy population.

Authors:  Xinyi Tang; Liyun Wang; Ruiqian Guo; Songya Huang; Yuanjiao Tang; Li Qiu
Journal:  Quant Imaging Med Surg       Date:  2020-10

Review 3.  Musculoskeletal conditions of the foot and ankle: assessments and treatment options.

Authors:  Smita Rao; Jody L Riskowski; Marian T Hannan
Journal:  Best Pract Res Clin Rheumatol       Date:  2012-06       Impact factor: 4.098

4.  Cyclosporine A in Ullrich congenital muscular dystrophy: long-term results.

Authors:  Luciano Merlini; Patrizia Sabatelli; Annarita Armaroli; Saverio Gnudi; Alessia Angelin; Paolo Grumati; Maria Elena Michelini; Andrea Franchella; Francesca Gualandi; Enrico Bertini; Nadir Mario Maraldi; Alessandra Ferlini; Paolo Bonaldo; Paolo Bernardi
Journal:  Oxid Med Cell Longev       Date:  2011-10-17       Impact factor: 6.543

5.  Quadriceps muscle strength in Duchenne muscular dystrophy and effect of corticosteroid treatment.

Authors:  Luciano Merlini; Ilaria Cecconi; Antonia Parmeggiani; Duccio Maria Cordelli; Ada Dormi
Journal:  Acta Myol       Date:  2020-12-01

6.  Body composition, muscle strength, and physical function of patients with Bethlem myopathy and Ullrich congenital muscular dystrophy.

Authors:  Maria Teresa Miscione; Francesca Bruno; Claudio Ripamonti; Giuliana Nervuti; Riccardo Orsini; Cesare Faldini; Massimo Pellegrini; Daniela Cocchi; Luciano Merlini
Journal:  ScientificWorldJournal       Date:  2013-09-12
  6 in total

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