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Pediatric Neurology
Volume 29, Issue 4
, Pages 337-340
, October 2003
Cervical myelopathy in an adolescent with hallervorden-spatz disease
References
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- Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13. Nat Genet. 1996;14:479–481
- A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome. Nat Genet. 2001;28:345–349
- . Cervical spondylosis and dyskinesias. Neurology. 1970;20:1194–1199
- . Unstable surgical spine in athetoid cerebral palsy. Spine. 1989;14:1154–1159
- . Severe motor tics causing cervical myelopathy in Tourette’s Syndrome. Mov Disord. 1996;11:563–566
- . Cervical spondylotic myeloradiculopathy in dystonia. Arch Phys Med Rehabil. 1992;73:389–392
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- Acquired cervical spine impairment in young adults with cerebral palsy. Dev Med Child Neurol. 1991;33:153–166
- Use of intrathecal baclofen in the treatment of patients with dystonia. Arch Neurol. 1996;53:1241–1246
- Stereostatic pallidotomy in a child with Hallervorden-Spatz disease. J Neurosurg. 1999;90:551–554
☆ From the Department of Pediatrics and Adolescent Medicine, Princess Margaret Hospital, 2-10 Princess Margaret Hospital Road, Lai Chi Kok, Kowloon, Hong Kong.
PII: S0887-8994(03)00272-8
doi: 10.1016/S0887-8994(03)00272-8
© 2003 Elsevier Inc. All rights reserved.
Next »
Pediatric Neurology
Volume 29, Issue 4
, Pages 337-340
, October 2003
