Literature DB >> 23524069

Neuromuscular junction disorders.

Chiawen Lucy Liang1, Steve Han.   

Abstract

Disorders of the neuromuscular junction, such as myasthenia gravis and Lambert-Eaton myasthenic syndrome, constitute an important and treatable class of diseases. Both disorders are typically caused by an immunologically mediated attack on discrete components of the neuromuscular junction, compromise the efficacy of neurotransmitter transmission, and produce clinically distinct syndromes of fatigable muscle weakness. Although the history, clinical examination, and routine antibody testing can be diagnostic in many cases, specialized neurophysiological tests, such as repetitive nerve stimulation and single-fiber electromyography, are essential tools in the diagnostic evaluation of patients with more complicated or atypical conditions. In this review, we introduce primary disorders of the neuromuscular junction, and discuss the salient clinical and laboratory workup appropriate for recognizing these disorders, and the typical findings seen on electrodiagnostic testing with repetitive nerve stimulation and single-fiber electromyography.
Copyright © 2013 American Academy of Physical Medicine and Rehabilitation. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23524069     DOI: 10.1016/j.pmrj.2013.03.016

Source DB:  PubMed          Journal:  PM R        ISSN: 1934-1482            Impact factor:   2.298


  3 in total

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Authors:  Katja A Puttonen; Marika Ruponen; Nikolay Naumenko; Outi H Hovatta; Pasi Tavi; Jari Koistinaho
Journal:  Front Cell Neurosci       Date:  2015-12-08       Impact factor: 5.505

2.  On-chip, multisite extracellular and intracellular recordings from primary cultured skeletal myotubes.

Authors:  Noha Rabieh; Silviya M Ojovan; Nava Shmoel; Hadas Erez; Eilon Maydan; Micha E Spira
Journal:  Sci Rep       Date:  2016-11-04       Impact factor: 4.379

3.  The p75NTR neurotrophin receptor is required to organize the mature neuromuscular synapse by regulating synaptic vesicle availability.

Authors:  Viviana Pérez; Francisca Bermedo-Garcia; Diego Zelada; Felipe A Court; Miguel Ángel Pérez; Marco Fuenzalida; Johanna Ábrigo; Claudio Cabello-Verrugio; Guillermo Moya-Alvarado; Juan Carlos Tapia; Vicente Valenzuela; Claudio Hetz; Francisca C Bronfman; Juan Pablo Henríquez
Journal:  Acta Neuropathol Commun       Date:  2019-09-12       Impact factor: 7.801

  3 in total

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