Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait
- 1 December 2003
- journal article
- Published by Wiley in Developmental Medicine and Child Neurology
- Vol. 45 (12), 833-836
- https://doi.org/10.1111/j.1469-8749.2003.tb00899.x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Alternating Hemiplegia of Childhood: No Mutations in the Familial Hemiplegic Migraine CACNA1A GeneCephalalgia, 2000
- Alternating hemiplegia of childhood: clinical manifestations and long-term outcomePediatric Neurology, 2000
- Alternating Hemiplegia of Childhood in Half-SistersJournal of Child Neurology, 2000
- Alternating Hemiplegia of Childhood: Insights Into Its PathophysiologyJournal of Child Neurology, 1998
- Alternating Hemiplegia of ChildhoodDevelopmental Medicine and Child Neurology, 1995
- Patient with unusual alternating hemiplegiaPediatric Neurology, 1994
- Alternating hemiplegia of childhoodThe Journal of Pediatrics, 1993
- A syndrome of autosomal dominant alternating hemiplegiaNeurology, 1992
- Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34Annals of Neurology, 1990
- Human gene for torsion dystonia located on chromosome 9q32-q34Neuron, 1989