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https://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 |
DOI: | 10.1002/mds.10469 |
Published version: | http://dx.doi.org/10.1002/mds.10469 |
Appears in Collections: | Aurora harvest Medicine publications |
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