Electroclinical Features and Long-Term Outcome of Cryptogenic Epilepsy in Children with Down Syndrome
- 1 December 2013
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 163 (6) , 1754-1758
- https://doi.org/10.1016/j.jpeds.2013.07.022
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Lennox‐Gastaut syndrome with late‐onset and prominent reflex seizures in trisomy 21 patientsEpilepsia, 2009
- Clinical and EEG Features of Epilepsy in Children and Adolescents in Down SyndromeJournal of Child Neurology, 2009
- Epidemiology of Down syndromeMental Retardation and Developmental Disabilities Research Reviews, 2007
- Down syndrome, Alzheimer's disease and seizuresBrain & Development, 2005
- The epidemiology of epilepsy in Europe – a systematic reviewEuropean Journal of Neurology, 2005
- Infantile spasms in Down syndrome—effects of delayed anticonvulsive treatmentEpilepsy Research, 2003
- Early Clinical and EEG Features of Infantile Spasms in Down SyndromeEpilepsia, 1996
- SEIZURES IN CHILDREN WITH DOWN SYNDROME: ETIOLOGY, CHARACTERISTICS AND OUTCOMEDevelopmental Medicine and Child Neurology, 1991
- Reflex Seizures are Frequent in Patients with Down Syndrome and EpilepsyEpilepsia, 1990
- A Prospective Study of Infantile Spasms: Clinical and Therapeutic CorrelationsEpilepsia, 1983