Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/36323
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Type: Journal article
Title: Myoclonus in spinal Dysraphism
Author: Warren, J.
Vidailhet, M.
Kneebone, C.
Quinn, N.
Thompson, P.
Citation: Movement Disorders, 2003; 18(8):961-964
Publisher: Wiley-Liss
Issue Date: 2003
ISSN: 0885-3185
1531-8257
Statement of
Responsibility: 
Jane E. Warren, Marie Vidailhet, Christopher S. Kneebone, Niall P. Quinn, Philip D. Thompson
Abstract: Two cases of segmental myoclonus occurring in association with spinal dysraphism are described. In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences.
Keywords: Spine; Spinal Cord; Humans; Spinal Dysraphism; Myoclonus; Magnetic Resonance Imaging; Electromyography; Severity of Illness Index; Adolescent; Child, Preschool; Female
Description: Copyright © 2003 Movement Disorder Society Published in Movement Disorders, 2003; 18 (8):961-964 at www.interscience.wiley.com
RMID: 0020030069
DOI: 10.1002/mds.10469
Appears in Collections:Medicine publications

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