Treatment of Epileptic Encephalopathies

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum

(2013) Amy McTague et al.   BRAIN

Efficacy of the ketogenic diet in Lennox-Gastaut syndrome: a retrospective review of one institution’s experience and summary of the literature

(2012) MONICA E LEMMON et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Sulthiame add-on therapy in children with focal epilepsies associated with encephalopathy related to electrical status epilepticus during slow sleep (ESES)

(2012) Natalio Fejerman et al.   EPILEPSIA

Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy

(2012) Annapurna Poduri et al.   EPILEPSIA

First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome)

(2012) C. von Stülpnagel et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy

(2012) Giulia Barcia et al.   NATURE GENETICS

Genetics of early-onset epilepsy with encephalopathy

(2012) Rima Nabbout et al.   Nature Reviews Neurology

Bromide in Patients with SCN1A-Mutations Manifesting as Dravet Syndrome

(2012) Jan Lotte et al.   NEUROPEDIATRICS

Light-activated channels in acute seizures

(2011) Merab Kokaia   EPILEPSIA

Nonpharmacologic treatments of Dravet syndrome: Focus on the ketogenic diet

(2011) Roberto Horacio Caraballo   EPILEPSIA

Long-term follow-up of febrile infection-related epilepsy syndrome

(2011) Katherine B. Howell et al.   EPILEPSIA

Febrile infection-related epilepsy syndrome (FIRES): Pathogenesis, treatment, and outcome

(2011) Uri Kramer et al.   EPILEPSIA

The effect of lead time to treatment and of age of onset on developmental outcome at 4 years in infantile spasms: Evidence from the United Kingdom Infantile Spasms Study

(2011) Finbar J. K. O’Callaghan et al.   EPILEPSIA

A review of the relationships between Landau–Kleffner syndrome, electrical status epilepticus during sleep, and continuous spike–waves during sleep

(2011) John R. Hughes   EPILEPSY & BEHAVIOR

Myoclonic astatic epilepsy: An age-dependent epileptic syndrome with favorable seizure outcome but variable cognitive evolution

(2011) Marina Trivisano et al.   EPILEPSY RESEARCH

Pyridoxine dependent epilepsy and antiquitin deficiency

(2011) Sylvia Stockler et al.   MOLECULAR GENETICS AND METABOLISM

De novo SCN1A mutations in migrating partial seizures of infancy

(2011) D. Carranza Rojo et al.   NEUROLOGY

The Fat Is in the Fire: Ketogenic Diet for Refractory Status Epilepticus

(2011) Eric Kossoff   Epilepsy Currents

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

(2010) W. G. Leen et al.   BRAIN

Developmental outcomes in children receiving resection surgery for medically intractable infantile spasms

(2010) Robert Asarnow et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Doose syndrome (myoclonic-astatic epilepsy): 40 years of progress

(2010) SARAH A KELLEY et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

The effect of surgery in encephalopathy with electrical status epilepticus during sleep

(2010) Maria E. Peltola et al.   EPILEPSIA

Infantile epileptic encephalopathy with late-onset spasms: Report of 19 patients

(2010) Stéphane Auvin et al.   EPILEPSIA

Prevalence of visual field loss following exposure to vigabatrin therapy: A systematic review

(2010) Melissa J. Maguire et al.   EPILEPSIA

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

Efficacy of Felbamate in the Treatment of Intractable Pediatric Epilepsy

(2010) Mary L. Zupanc et al.   PEDIATRIC NEUROLOGY

Mutations in the mitochondrial glutamate carrierSLC25A22in neonatal epileptic encephalopathy with suppression bursts

(2009) F Molinari et al.   CLINICAL GENETICS

Visual Field Loss in Patients with Refractory Partial Epilepsy Treated with Vigabatrin

(2009) John M. Wild et al.   CNS DRUGS

The surgical treatment of Landau-Kleffner syndrome

(2009) J. Helen Cross et al.   EPILEPSIA

Corticosteroids as treatment of epileptic syndromes with continuous spike-waves during slow-wave sleep

(2009) Marga Buzatu et al.   EPILEPSIA

Visual fields at school-age in children treated with vigabatrin in infancy

(2009) Eija Gaily et al.   EPILEPSIA

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

(2009) Christel Depienne et al.   PLoS Genetics

The ketogenic diet for the treatment of childhood epilepsy: a randomised controlled trial

(2008) Elizabeth G Neal et al.   LANCET NEUROLOGY

Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology

(2008) Alexis Arzimanoglou et al.   LANCET NEUROLOGY

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

(2008) Hirotomo Saitsu et al.   NATURE GENETICS

Rufinamide for generalized seizures associated with Lennox-Gastaut syndrome

(2008) T. Glauser et al.   NEUROLOGY