Treatment of Epileptic Encephalopathies
暂无分享,去创建一个
[1] C. Ferrie,et al. Corticosteroids including ACTH for childhood epilepsy other than epileptic spasms. , 2015, The Cochrane database of systematic reviews.
[2] I. Scheffer,et al. Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum. , 2013, Brain : a journal of neurology.
[3] L. Kaczmarek,et al. De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy , 2012, Nature Genetics.
[4] P. Striano,et al. First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome). , 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
[5] I. Scheffer,et al. Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy , 2012, Epilepsia.
[6] N. Fejerman,et al. Sulthiame add‐on therapy in children with focal epilepsies associated with encephalopathy related to electrical status epilepticus during slow sleep (ESES) , 2012, Epilepsia.
[7] E. Kossoff,et al. Efficacy of the ketogenic diet in Lennox–Gastaut syndrome: a retrospective review of one institution’s experience and summary of the literature , 2012, Developmental medicine and child neurology.
[8] C. Tassinari,et al. Therapy of encephalopathy with status epilepticus during sleep (ESES/CSWS syndrome): an update , 2012, Epileptic disorders : international epilepsy journal with videotape.
[9] M. Staudt,et al. Bromide in Patients with SCN1A-Mutations Manifesting as Dravet Syndrome , 2012, Neuropediatrics.
[10] O. Dulac,et al. Epilepsy: Genetics of early-onset epilepsy with encephalopathy , 2012, Nature Reviews Neurology.
[11] I. Scheffer,et al. Long‐term follow‐up of febrile infection–related epilepsy syndrome , 2012, Epilepsia.
[12] F. Vigevano,et al. Myoclonic astatic epilepsy: An age-dependent epileptic syndrome with favorable seizure outcome but variable cognitive evolution , 2011, Epilepsy Research.
[13] M. Sahin,et al. Febrile infection–related epilepsy syndrome (FIRES): Pathogenesis, treatment, and outcome , 2011, Epilepsia.
[14] M. Kokaia. Light‐activated channels in acute seizures , 2011, Epilepsia.
[15] C. V. van Karnebeek,et al. Pyridoxine dependent epilepsy and antiquitin deficiency: clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up. , 2011, Molecular genetics and metabolism.
[16] I. Scheffer,et al. De novo SCN1A mutations in migrating partial seizures of infancy , 2011, Neurology.
[17] J. Osborne,et al. 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, Epilepsia.
[18] E. Kossoff. The Fat is in the Fire: Ketogenic Diet for Refractory Status Epilepticus , 2011, Epilepsy Currents.
[19] R. Caraballo. Nonpharmacologic treatments of Dravet syndrome: Focus on the ketogenic diet , 2011, Epilepsia.
[20] T. Resnick,et al. All children who experience epileptic falls do not necessarily have Lennox-Gastaut syndrome... but many do. , 2011, Epileptic disorders : international epilepsy journal with videotape.
[21] B. Falck,et al. The effect of surgery in encephalopathy with electrical status epilepticus during sleep , 2011, Epilepsia.
[22] J. R. Hughes. A review of the relationships between Landau–Kleffner syndrome, electrical status epilepticus during sleep, and continuous spike–waves during sleep , 2011, Epilepsy & Behavior.
[23] A. Marson,et al. Prevalence of visual field loss following exposure to vigabatrin therapy: A systematic review , 2010, Epilepsia.
[24] E. Kossoff,et al. Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress , 2010, Developmental medicine and child neurology.
[25] L. Vallée,et al. Infantile epileptic encephalopathy with late‐onset spasms: Report of 19 patients , 2010, Epilepsia.
[26] C. Marcuccilli,et al. Efficacy of felbamate in the treatment of intractable pediatric epilepsy. , 2010, Pediatric neurology.
[27] J. H. Cross,et al. Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009 , 2010, Epilepsia.
[28] B. Weschke,et al. Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder. , 2010, Brain : a journal of neurology.
[29] M. Baulac,et al. Visual Field Loss in Patients with Refractory Partial Epilepsy Treated with Vigabatrin , 2009, CNS drugs.
[30] J. H. Cross,et al. The surgical treatment of Landau‐Kleffner syndrome , 2009, Epilepsia.
[31] A. Munnich,et al. Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts , 2009, Clinical genetics.
[32] O. Dulac,et al. Corticosteroids as treatment of epileptic syndromes with continuous spike‐waves during slow‐wave sleep , 2009, Epilepsia.
[33] E. Gaily,et al. Visual fields at school‐age in children treated with vigabatrin in infancy , 2009, Epilepsia.
[34] M. Ruberg,et al. Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females , 2009, PLoS genetics.
[35] J. Cross,et al. Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology , 2009, Lancet Neurology.
[36] J. Cross,et al. The ketogenic diet for the treatment of childhood epilepsy: a randomised controlled trial , 2008, The Lancet Neurology.
[37] G. Krauss,et al. Rufinamide for generalized seizures associated with Lennox–Gastaut syndrome , 2008, Neurology.
[38] Naomichi Matsumoto,et al. De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy , 2008, Nature Genetics.
[39] Shinji Saitoh,et al. A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome). , 2007, American journal of human genetics.
[40] A. Barkovich,et al. Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus , 2007, Neurology.
[41] E Wyllie,et al. Successful surgery for epilepsy due to early brain lesions despite generalized EEG findings , 2007, Neurology.
[42] M. Baumgartner,et al. Pyridoxal 5′-phosphate may be curative in early-onset epileptic encephalopathy , 2007, Journal of Inherited Metabolic Disease.
[43] Janez Stare,et al. The Risk of Lower Mental Outcome in Infantile Spasms Increases after Three Weeks of Hypsarrhythmia Duration , 2006, Epilepsia.
[44] N. Fejerman,et al. Ketogenic diet in patients with myoclonic-astatic epilepsy. , 2006, Epileptic disorders : international epilepsy journal with videotape.
[45] J. Tolmie,et al. CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients , 2006, Journal of Medical Genetics.
[46] J. Osborne,et al. The United Kingdom Infantile Spasms Study (UKISS) comparing hormone treatment with vigabatrin on developmental and epilepsy outcomes to age 14 months: a multicentre randomised trial , 2005, The Lancet Neurology.
[47] L. Lagae,et al. Steroids in intractable childhood epilepsy: Clinical experience and review of the literature , 2005, Seizure.
[48] D. Kwiatkowski,et al. Infantile spasms and intellectual outcomes in children with tuberous sclerosis complex , 2005, Neurology.
[49] A. Munnich,et al. Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy. , 2005, American journal of human genetics.
[50] S. Shinnar,et al. Long‐term Cognitive Outcomes of a Cohort of Children with Cryptogenic Infantile Spasms Treated with High‐dose Adrenocorticotropic Hormone , 2004, Epilepsia.
[51] P. Veggiotti,et al. Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial , 2002, Epilepsy Research.
[52] S. Ohtahara,et al. Early-infantile epileptic encephalopathy with suppression-bursts, Ohtahara syndrome; its overview referring to our 16 cases , 2002, Brain and Development.
[53] L. Lagae,et al. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. , 2001, American journal of human genetics.
[54] T. Glauser. Topiramate in the Catastrophic Epilepsies of Childhood , 2000, Journal of child neurology.
[55] O. Dulac,et al. Stiripentol in severe myoclonic epilepsy in infancy: a randomised placebo-controlled syndrome-dedicated trial , 2000, The Lancet.
[56] Naoyuki Kitamura,et al. Successful control with bromide of two patients with malignant migrating partial seizures in infancy , 2000, Brain and Development.
[57] H. Takada,et al. Neurotrophin-3 Levels in Cerebrospinal Fluid From Children With Bacterial Meningitis, Viral Meningitis, or Encephalitis , 2000, Journal of child neurology.
[58] R. Asarnow,et al. Developmental outcomes in children receiving resection surgery for medically intractable infantile spasms , 1997, Developmental medicine and child neurology.
[59] E. Oka,et al. The early-infantile epileptic encephalopathy with suppression-burst: Developmental aspects , 1987, Brain and Development.
[60] 俊輔 大田原,et al. 特異な年齢依存性てんかん性脳症The Early-Infantile Epileptic Encephalopathy with Suppression-Burstに関する研究 , 1976 .
[61] H. Cross,et al. Corticosteroids including ACTH for childhood epilepsy other than epileptic spasms. , 2007, The Cochrane database of systematic reviews.