Chapter 12 Motor unit number estimation in the upper trapezius muscle

Supplements to Clinical Neurophysiology

Volumn 60, Issue C, 2009, Pages 131-134

  Lewis, Richard A ^a  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTION POTENTIAL; ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MIDDLE AGED; MOTONEURON; NECK MUSCLE; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; SPINAL MUSCULAR ATROPHY;

ACTION POTENTIALS; ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; CHARCOT-MARIE-TOOTH DISEASE; FEMALE; HUMANS; MALE; MIDDLE AGED; MOTOR NEURONS; MUSCULAR ATROPHY, SPINAL; NECK MUSCLES; YOUNG ADULT;

EID: 77956637449     PISSN: 1567424X     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1567-424X(08)00012-3     Document Type: Chapter

References (8)

1. Boe S.G., Stashuk D.W., and Doherty T.J. Motor unit number estimation by decomposition-enhanced spike-triggered averaging: control data, test-retest reliability, and contractile level effects. Muscle Nerve 29 (2004) 693-699
2. Boe S.G., Stashuk D.W., and Doherty T.J. Motor unit number estimates and quantitative motor unit analysis in healthy subjects and patients with amyotrophic lateral sclerosis. Muscle Nerve 36 (2007) 62-70
3. Lachman N., Acland R.D., and Rosse C. Anatomical evidence for the absence of a morphologically distinct cranial root of the accessory nerve in man. Clin. Anat. 15 (2002) 4-10
4. Lawson V.H., Gordon Smith A., and Bromberg M.B. Assessment of axonal loss in Charcot-Marie-Tooth neuropathies. Exp. Neurol. 184 (2003) 753-757
5. Lawson V.H., Bromberg M.B., and Stashuk D. Comparison of conventional and decomposition-enhanced spike triggered averaging techniques. Clin. Neurophysiol. 115 (2004) 564-568
6. Lewis R.A., Li J., Fuerst D.R., Shy M.E., and Krajewski K. Motor unit number estimate of distal and proximal muscles in Charcot-Marie-Tooth disease. Muscle Nerve 28 (2003) 161-167
7. Shy M.E., Siskind C., Swan E.R., Krajewski K.M., Doherty T., Fuerst D.R., Ainsworth P.J., Lewis R.A., Scherer S.S., and Hahn A.F. CMT1X phenotypes represent loss of GJB1 gene function. Neurology 68 (2007) 849-855
8. Stashuk D.W. Decomposition and quantitative analysis of clinical electromyographic signals. Med. Eng. Phys. 21 (1999) 389-404