| P2093 | author name string | Sharon Whiting | |
| | Elaine Wirrell | |
| | Kevin Farrell | |
| P2860 | cites work | Stiripentol in severe myoclonic epilepsy in infancy: a randomised placebo-controlled syndrome-dedicated trial. STICLO study group | Q28138394 |
| | Language outcome following multiple subpial transection for Landau-Kleffner syndrome | Q28139885 |
| | Experience with the ketogenic diet in infants | Q28204324 |
| | Efficacy of the ketogenic diet for infantile spasms | Q28216365 |
| | Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy | Q28243859 |
| | Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity | Q28274128 |
| | Psychological effects of sodium valproate and carbamazepine in epilepsy | Q28317913 |
| | Side effects of phenobarbital in toddlers; behavioral and cognitive aspects | Q28325110 |
| | Phenobarbital for febrile seizures--effects on intelligence and on seizure recurrence | Q28332044 |
| | Practice parameter: medical treatment of infantile spasms: report of the American Academy of Neurology and the Child Neurology Society | Q30496557 |
| | Long-term seizure outcome in 74 patients with Lennox-Gastaut syndrome: effects of incorporating MRI head imaging in defining the cryptogenic subgroup | Q30589418 |
| | Ketogenic diet for the treatment of refractory epilepsy in children: A systematic review of efficacy | Q30853260 |
| | Vigabatrin in the treatment of infantile spasms in tuberous sclerosis: literature review | Q33540388 |
| | Piracetam in the treatment of cortical myoclonus. | Q33641369 |
| | A double-blind, randomized trial of topiramate in Lennox-Gastaut syndrome. Topiramate YL Study Group | Q33865133 |
| | Refractory idiopathic absence status epilepticus: A probable paradoxical effect of phenytoin and carbamazepine | Q33969852 |
| | Double-blind study of ACTH vs prednisone therapy in infantile spasms | Q34255001 |
| | Lennox-Gastaut syndrome (childhood epileptic encephalopathy). | Q34291322 |
| | Landau-Kleffner syndrome. Treatment with subpial intracortical transection | Q34374475 |
| | Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome). | Q34432842 |
| | Lamotrigine for generalized seizures associated with the Lennox-Gastaut syndrome. Lamictal Lennox-Gastaut Study Group | Q34449487 |
| | A multicenter study of the efficacy of the ketogenic diet. | Q34480837 |
| | The efficacy of the ketogenic diet-1998: a prospective evaluation of intervention in 150 children | Q34481820 |
| | Non-convulsive status epilepticus. | Q34796648 |
| | Non-convulsive status epilepticus resistant to benzodiazepines | Q35603435 |
| | Effects of epileptiform EEG discharges on cognitive function: is the concept of "transient cognitive impairment" still valid? | Q35630237 |
| | Cognitive side effects of antiepileptic drugs in children | Q35705773 |
| | Neuroepileptic correlates of autistic symptomatology in tuberous sclerosis | Q35884877 |
| | A proposal for case definitions and outcome measures in studies of infantile spasms and West syndrome: consensus statement of the West Delphi group | Q35929989 |
| | The Lennox-Gastaut syndrome | Q40781651 |
| | Multiple subpial transection for Landau-Kleffner syndrome | Q41003968 |
| | Transient cognitive impairment during subclinical epileptiform electroencephalographic discharges | Q41677394 |
| | Exacerbation of seizures in children by carbamazepine | Q42226065 |
| | Tonic Status Epilepticus precipitated by Intravenous Benzodiazepine in Five Patients with Lennox-Gastaut Syndrome | Q42233834 |
| | Myoclonic, atonic, and absence seizures following institution of carbamazepine therapy in children | Q42248685 |
| | Zonisamide for progressive myoclonus epilepsy: long-term observations in seven patients | Q42544838 |
| | Landau-Kleffner Syndrome: A Pharmacologic Study of Five Cases | Q43521841 |
| | Incidence of drug-induced aggravation in benign epilepsy with centrotemporal spikes | Q43650815 |
| | Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial | Q43955548 |
| | Topiramate as add-on drug in children, adolescents and young adults with Lennox-Gastaut syndrome: an Italian multicentric study | Q44154788 |
| | Prospective preliminary analysis of the development of autism and epilepsy in children with infantile spasms | Q44430244 |
| | Long-term cognitive outcomes of a cohort of children with cryptogenic infantile spasms treated with high-dose adrenocorticotropic hormone | Q44792014 |
| | Developmental outcomes in children receiving resection surgery for medically intractable infantile spasms. | Q46519316 |
| | A comparative study of high-dose and low-dose ACTH therapy for West syndrome | Q48090381 |
| | Folinic acid-responsive neonatal seizures | Q48130929 |
| | Surgery for intractable infantile spasms: neuroimaging perspectives | Q48258361 |
| | Effectiveness of piracetam in cortical myoclonus | Q48364687 |
| | Atypical Lennox-Gastaut syndrome successfully treated with removal of a parietal dysembryoplastic tumour. | Q48572975 |
| | Behavioural and neuropsychological problems in refractory paediatric epilepsies | Q48573459 |
| | Generalized sharp and slow wave complexes. Associated clinical features and long-term follow-up | Q48656299 |
| | Hypsarrhythmia: variations on the theme | Q48662299 |
| | Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: symptomatology and long-term prognosis | Q48696037 |
| | Multiple subpial transection in Landau-Kleffner syndrome | Q48696689 |
| | Clinical trial of piracetam in patients with myoclonus: nationwide multiinstitution study in Japan. The Myoclonus/Piracetam Study Group | Q48880494 |
| | Psychiatric disorder among children with tuberous sclerosis | Q50308353 |
| | Mental and behavioural outcome of infantile epilepsy treated by vigabatrin in tuberous sclerosis patients | Q50313281 |
| | Psychiatric disorders in children with earlier infantile spasms | Q50346036 |
| | Biotinidase deficiency: initial clinical features and rapid diagnosis. | Q50582092 |
| | Long-term effects of 24-month treatment with vagus nerve stimulation on behaviour in children with Lennox-Gastaut syndrome. | Q51950285 |
| | Nonconvulsive status epilepticus--a possible cause of mental retardation in patients with Lennox-Gastaut syndrome. | Q51972328 |
| | Corpus callosotomy in treatment of medically resistant epilepsy: preliminary results in a pediatric population. | Q52033512 |
| | A double-blind, randomized trial of topiramate as adjunctive therapy for partial-onset seizures in children. Topiramate YP Study Group. | Q52034189 |
| | Withdrawal of antiepileptic medication in children--effects on cognitive function: The Multicenter Holmfrid Study. | Q52039141 |
| | Cognitive Impairment in New Cases of Epilepsy Randomly Assigned to Carbamazepine, Phenytoin and Sodium Valproate | Q52098377 |
| | Migrating partial seizures in infancy: a malignant disorder with developmental arrest. | Q52205836 |
| | Vagus nerve stimulation in children with refractory seizures associated with Lennox-Gastaut syndrome. | Q53472676 |
| | Vagal nerve stimulation in epileptic encephalopathies. | Q53555111 |
| | Treatment and long-term prognosis of myoclonic-astatic epilepsy of early childhood. | Q53960597 |
| | Vagus nerve stimulation treatment for Lennox-Gastaut syndrome. | Q54039142 |
| | Sulthiame as Monotherapy in Children with Benign Childhood Epilepsy with Centrotemporal Spikes: A 6-Month Randomized, Double-Blind, Placebo-Controlled Study | Q59280143 |
| | The Efficacy of Lamotrigine in Children and Adolescents with Refractory Generalized Epilepsy: A Randomized, Double-Blind, Crossover Study | Q61764267 |
| | Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy | Q62376625 |
| | Two cases of nonconvulsive status epilepticus in association with tiagabine therapy | Q62869102 |
| | A Prospective Study of Infantile Spasms: Clinical and Therapeutic Correlations | Q67274853 |
| | Effect of Early Corticosteroid Therapy for Landau-Kleffner Syndrome | Q67689038 |
| | Intravenous immunoglobulin: a single-blind trial in children with Lennox-Gastaut syndrome | Q68520517 |
| | Non-convulsive status epilepticus | Q69742846 |
| | ACTH and prednisone in childhood seizure disorders | Q70155018 |
| | Seizure and EEG patterns in Angelman's syndrome | Q70938447 |
| | Long-term prognosis of Lennox-Gastaut syndrome | Q71193172 |
| | Cortical myoclonus in Angelman syndrome | Q71209362 |
| | Influence of phenobarbital on the psychomotor development and behaviour in preschool children with convulsions | Q71851388 |
| | Treatment of refractory epilepsy with intravenous immunoglobulins. Results of the first double-blind/dose finding clinical study | Q72404468 |
| | High-dose, long-duration versus low-dose, short-duration corticotropin therapy for infantile spasms | Q72405400 |
| | "Baltic" myoclonus epilepsy: hereditary disorder of childhood made worse by phenytoin | Q72562516 |
| | Effects of high-dose intravenous corticosteroid therapy in Landau-Kleffner syndrome | Q73596737 |
| | Long-term seizure outcome following corpus callosotomy in children | Q73894072 |
| | Effects of ketogenic diet on development and behavior: preliminary report of a prospective study | Q73917020 |
| | Seizures induced or aggravated by anticonvulsants | Q93557602 |
| P433 | issue | 4 | |
| P921 | main subject | infancy stage | Q49257364 |
| P304 | page(s) | 409-418 | |
| P577 | publication date | 2005-11-01 | |
| P1433 | published in | Canadian Journal of Neurological Sciences | Q5030246 |
| P1476 | title | The epileptic encephalopathies of infancy and childhood | |
| P478 | volume | 32 | |