Published in Brain Dev on March 01, 2005
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Symptoms of narcolepsy in children misinterpreted as epilepsy. Epileptic Disord (2005) 0.87
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De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin. J Med Genet (2009) 0.85
The movement disorders of Coffin-Lowry syndrome. Brain Dev (2005) 0.85
Psychosocial and intellectual functioning in childhood narcolepsy. Dev Neurorehabil (2008) 0.84
Mind-stretching faints. Epileptic Disord (2007) 0.84
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Shaken baby syndrome. J R Soc Med (2003) 0.75
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Childhood convulsive status epilepticus. Lancet (2006) 0.75
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Stuart Green's vignettes 7 and 8. Eur J Paediatr Neurol (2008) 0.75
Identification of novel mutations in patients with Coffin-Lowry syndrome by a denaturing HPLC-based assay. Clin Chem (2005) 0.75
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Stuart Green's vignettes 3 and 4. Eur J Paediatr Neurol (2008) 0.75
Stuart Green's vignettes 9 and 10. Eur J Paediatr Neurol (2008) 0.75
Developmental outcome in benign myoclonic epilepsy in infancy and reflex myoclonic epilepsy in infancy: a literature review and six new cases. Epilepsy Res (2006) 0.75
Stuart Green's Vignettes 17 and 18. Eur J Paediatr Neurol (2009) 0.75
Advances in epilepsy gene discovery and implications for epilepsy diagnosis and treatment. Curr Opin Neurol (2017) 0.75
Stuart Green's vignettes 5 and 6. Eur J Paediatr Neurol (2008) 0.75
Hepatic coma culminating in severe brain damage in a child with a SCN1A mutation. Eur J Paediatr Neurol (2010) 0.75