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ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archneurol.2011.3275openalex-snapshot
Progressive Gait Deterioration in Adolescents With Dravet Syndrome
inferredcites →https://doi.org/10.1002/1531-8249(199901)45:1<75::aid-art13>3.0.co;2-wopenalex-snapshot
Generalized epilepsy with febrile seizures plus: A common childhood-onset genetic epilepsy syndrome
inferredcites →https://doi.org/10.1002/ajmg.1320160417openalex-snapshot
Benign familial neonatal‐infantile seizures
inferredcites →https://doi.org/10.1002/ajmg.1320570110openalex-snapshot
Outcome of Sturge‐Weber syndrome in 52 adults
inferredcites →https://doi.org/10.1002/ana.20029openalex-snapshot
Benign familial neonatal‐infantile seizures: Characterization of a new sodium channelopathy
inferredcites →https://doi.org/10.1002/ana.22644openalex-snapshot
KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy
inferredcites →https://doi.org/10.1002/ana.24580openalex-snapshot
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
inferredcites →https://doi.org/10.1002/ana.24883openalex-snapshot
Genetics and genotype–phenotype correlations in early onset epileptic encephalopathy with burst suppression
inferredcites →https://doi.org/10.1002/ana.24970openalex-snapshot
A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome
inferredcites →https://doi.org/10.1002/ana.25438openalex-snapshot
SCN1A gain of function in early infantile encephalopathy
inferredcites →https://doi.org/10.1002/ana.25619openalex-snapshot
The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures
inferredcites →https://doi.org/10.1002/ana.410340613openalex-snapshot
Electroclinical signs of benign neonatal familial convulsions
inferredcites →https://doi.org/10.1002/epi4.12225openalex-snapshot
Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group
inferredcites →https://doi.org/10.1002/epi4.12414openalex-snapshot
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group
inferredcites →https://doi.org/10.1002/jimd.12045openalex-snapshot
The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy
inferredcites →https://doi.org/10.1002/jimd.12332openalex-snapshot
Consensus guidelines for the diagnosis and management of pyridoxine‐dependent epilepsy due to α‐aminoadipic semialdehyde dehydrogenase deficiency
inferredcites →https://doi.org/10.1007/8904_2015_456openalex-snapshot
PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?
inferredcites →https://doi.org/10.1007/8904_2015_482openalex-snapshot
Normal Neurodevelopmental Outcomes in PNPO Deficiency: A Case Series and Literature Review
inferredcites →https://doi.org/10.1007/978-3-319-01366-4_9openalex-snapshot
Generalized Epilepsy with Febrile Seizures Plus
inferredcites →https://doi.org/10.1007/bf01957732openalex-snapshot
Benign infantile familial convulsions
inferredcites →https://doi.org/10.1007/s00415-014-7240-zopenalex-snapshot
GLUT1 deficiency syndrome into adulthood: a follow-up study
inferredcites →https://doi.org/10.1007/s00415-014-7433-5openalex-snapshot
Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature
inferredcites →https://doi.org/10.1007/s10048-017-0517-5openalex-snapshot
Male patients affected by mosaic PCDH19 mutations: five new cases
inferredcites →https://doi.org/10.1007/s10545-018-0219-7openalex-snapshot
The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: a common epileptic encephalopathy
inferredcites →https://doi.org/10.1016/0887-8994(86)90018-4openalex-snapshot
Benign familial neonatal seizures: Clinical and electroencephalographic characteristics
inferredcites →https://doi.org/10.1016/b978-0-444-59565-2.00050-2openalex-snapshot
Pyridoxine and pyridoxalphosphate-dependent epilepsies
inferredcites →https://doi.org/10.1016/j.ajhg.2016.05.031openalex-snapshot
Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy
inferredcites →https://doi.org/10.1016/j.ajhg.2016.10.011openalex-snapshot
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy
inferredcites →https://doi.org/10.1016/j.braindev.2003.12.012openalex-snapshot
Benign familial infantile seizures
inferredcites →https://doi.org/10.1016/j.braindev.2004.04.011openalex-snapshot
Benign myoclonic epilepsy in infancy: neuropsychological and behavioural outcome
inferredcites →https://doi.org/10.1016/j.braindev.2005.05.001openalex-snapshot
‘Benign focal epilepsy in infancy with vertex spikes and waves during sleep’. Delineation of the syndrome and recalling as ‘benign infantile focal epilepsy with midline spikes and waves during sleep’ (BIMSE)
inferredcites →https://doi.org/10.1016/j.braindev.2009.09.014openalex-snapshot
Dravet syndrome: Early clinical manifestations and cognitive outcome in 37 Italian patients
inferredcites →https://doi.org/10.1016/j.braindev.2010.10.009openalex-snapshot
Epilepsies and epileptic syndromes starting in the neonatal period
inferredcites →https://doi.org/10.1016/j.braindev.2011.11.011openalex-snapshot
A case of malignant migrating partial seizures in infancy as a continuum of infantile epileptic encephalopathy
inferredcites →https://doi.org/10.1016/j.braindev.2013.10.008openalex-snapshot
Infantile spasms syndrome, West syndrome and related phenotypes: What we know in 2013
inferredcites →https://doi.org/10.1016/j.ejpn.2003.10.003openalex-snapshot
Hypothalamic hamartoma with gelastic seizures in Swedish children and adolescents
inferredcites →https://doi.org/10.1016/j.ejpn.2004.03.001openalex-snapshot
Epileptic Syndromes in Infancy, Childhood and Adolescence
inferredcites →https://doi.org/10.1016/j.ejpn.2013.11.005openalex-snapshot
A proposed diagnostic approach for infantile spasms based on a spectrum of variable aetiology
inferredcites →https://doi.org/10.1016/j.ejpn.2014.04.008openalex-snapshot
Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings
inferredcites →https://doi.org/10.1016/j.ejpn.2018.02.002openalex-snapshot
GLUT-1 deficiency presenting with seizures and reversible leukoencephalopathy on MRI imaging
inferredcites →https://doi.org/10.1016/j.ejpn.2018.03.009openalex-snapshot
Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?
inferredcites →https://doi.org/10.1016/j.ejpn.2019.12.002openalex-snapshot
Genetic potassium channel-associated epilepsies: Clinical review of the Kv family
inferredcites →https://doi.org/10.1016/j.eplepsyres.2005.11.022openalex-snapshot
Are early myoclonic encephalopathy (EME) and the Ohtahara syndrome (EIEE) independent of each other?
inferredcites →https://doi.org/10.1016/j.eplepsyres.2006.01.014openalex-snapshot
Developmental outcome in benign myoclonic epilepsy in infancy and reflex myoclonic epilepsy in infancy: A literature review and six new cases
inferredcites →https://doi.org/10.1016/j.eplepsyres.2008.04.015openalex-snapshot
An unexpected EEG course in Dravet syndrome
inferredcites →https://doi.org/10.1016/j.eplepsyres.2011.03.009openalex-snapshot
Incidence and classification of new-onset epilepsy and epilepsy syndromes in children in Olmsted County, Minnesota from 1980 to 2004: A population-based study
inferredcites →https://doi.org/10.1016/j.eplepsyres.2013.03.002openalex-snapshot
Early onset epilepsy is associated with increased mortality: A population-based study
inferredcites →https://doi.org/10.1016/j.eplepsyres.2014.01.023openalex-snapshot
EEG evolution in Sturge-Weber syndrome
inferredcites →https://doi.org/10.1016/j.eplepsyres.2014.11.007openalex-snapshot
Topography of brain glucose hypometabolism and epileptic network in glucose transporter 1 deficiency
inferredcites →https://doi.org/10.1016/j.eplepsyres.2018.02.003openalex-snapshot
Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy
inferredcites →https://doi.org/10.1016/j.eplepsyres.2018.03.020openalex-snapshot
Spikes might precede seizures and predict epilepsy in children with Sturge-Weber syndrome: A pilot study
inferredcites →https://doi.org/10.1016/j.jaad.2014.11.009openalex-snapshot
A prospective study of risk for Sturge-Weber syndrome in children with upper facial port-wine stain
inferredcites →https://doi.org/10.1016/j.ncl.2016.06.015openalex-snapshot
The Epidemiology of Global Epilepsy
inferredcites →https://doi.org/10.1016/j.nicl.2016.12.026openalex-snapshot
Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2007.03.003openalex-snapshot
Pediatric-Onset Gelastic Seizures: Clinical Data and Outcome
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2007.03.009openalex-snapshot
GLUT1 Deficiency With Delayed Myelination Responding to Ketogenic Diet
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2011.01.005openalex-snapshot
Clinical Outcomes in Bilateral Sturge-Weber Syndrome
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2015.11.005openalex-snapshot
Sturge-Weber Syndrome: Brain Magnetic Resonance Imaging and Neuropathology Findings
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2016.05.012openalex-snapshot
Predictors of Cognitive Functions in Children With Sturge–Weber Syndrome: A Longitudinal Study
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2017.01.025openalex-snapshot
Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2018.04.012openalex-snapshot
Infantile Spasms of Unknown Cause: Predictors of Outcome and Genotype-Phenotype Correlation
inferredcites →https://doi.org/10.1016/j.pediatrneurol.2019.02.015openalex-snapshot
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review
inferredcites →https://doi.org/10.1016/j.seizure.2016.01.006openalex-snapshot
Effectiveness of antiepileptic therapy in patients with PCDH19 mutations
inferredcites →https://doi.org/10.1016/j.seizure.2018.05.005openalex-snapshot
Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy
inferredcites →https://doi.org/10.1016/j.spen.2015.10.005openalex-snapshot
Current Therapeutic Options in Sturge-Weber Syndrome
inferredcites →https://doi.org/10.1016/j.spen.2016.06.004openalex-snapshot
Amenable Treatable Severe Pediatric Epilepsies
inferredcites →https://doi.org/10.1016/j.spen.2019.08.006openalex-snapshot
Neonatal Developmental and Epileptic Encephalopathies
inferredcites →https://doi.org/10.1016/j.yebeh.2013.11.021openalex-snapshot
Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndrome
inferredcites →https://doi.org/10.1016/j.yebeh.2016.04.009openalex-snapshot
Autism spectrum disorder phenotype and intellectual disability in females with epilepsy and PCDH-19 mutations
inferredcites →https://doi.org/10.1016/j.yebeh.2017.05.037openalex-snapshot
Age-related “Sleep/nocturnal” tonic and tonic clonic seizure clusters are underdiagnosed in patients with Dravet Syndrome
inferredcites →https://doi.org/10.1016/j.yebeh.2018.05.015openalex-snapshot
Causes of mortality in early infantile epileptic encephalopathy: A systematic review
inferredcites →https://doi.org/10.1016/j.yebeh.2019.106539openalex-snapshot
The role of PCDH19 in refractory status epilepticus
inferredcites →https://doi.org/10.1016/j.ymgme.2011.05.014openalex-snapshot
Pyridoxine dependent epilepsy and antiquitin deficiency
inferredcites →https://doi.org/10.1016/j.yoph.2013.08.003openalex-snapshot
10.1016/j.yoph.2013.08.003
inferredcites →https://doi.org/10.1016/s0022-3476(99)70307-0openalex-snapshot
Demographics and diagnosis of pyridoxine-dependent seizures
inferredcites →https://doi.org/10.1016/s0140-6736(02)09968-3openalex-snapshot
Sodium-channel defects in benign familial neonatal-infantile seizures
inferredcites →https://doi.org/10.1016/s0140-6736(12)61381-6openalex-snapshot
Epilepsy in poor regions of the world
inferredcites →https://doi.org/10.1016/s0387-7604(01)00263-7openalex-snapshot
Epidemiological data of West syndrome in Finland
inferredcites →https://doi.org/10.1016/s0387-7604(01)00280-7openalex-snapshot
Video/EEG aspects of early-infantile epileptic encephalopathy with suppression-bursts (Ohtahara syndrome)
inferredcites →https://doi.org/10.1016/s0387-7604(01)00386-2openalex-snapshot
History of clinical identification of West syndrome – in quest after the classic
inferredcites →https://doi.org/10.1016/s0387-7604(97)00060-0openalex-snapshot
Benign myoclonic epilepsy: long-term follow-up of 11 new cases
inferredcites →https://doi.org/10.1016/s0887-8994(00)00127-2openalex-snapshot
Sturge-Weber syndrome without facial nevus
inferredcites →https://doi.org/10.1016/s0887-8994(98)00058-7openalex-snapshot
Neuroradiologic aspects of West syndrome
inferredcites →https://doi.org/10.1016/s0920-1211(03)00037-8openalex-snapshot
Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2
inferredcites →https://doi.org/10.1017/cbo9780511921001.066openalex-snapshot
Hypothalamic hamartoma and gelastic epilepsy
inferredcites →https://doi.org/10.1017/s0317167100008878openalex-snapshot
Sturge-Weber Syndrome. Study of 55 Patients
inferredcites →https://doi.org/10.1038/1252openalex-snapshot
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
inferredcites →https://doi.org/10.1038/74159openalex-snapshot
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
inferredcites →https://doi.org/10.1038/ejhg.2012.156openalex-snapshot
The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy
inferredcites →https://doi.org/10.1038/gim.2015.186openalex-snapshot
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy
inferredcites →https://doi.org/10.1038/ng.2441openalex-snapshot
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy
inferredcites →https://doi.org/10.1038/ng0198-25openalex-snapshot
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
inferredcites →https://doi.org/10.1038/ng0198-53openalex-snapshot
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
inferredcites →https://doi.org/10.1038/s41380-018-0066-9openalex-snapshot
A systematic review and meta-analysis of 271 PCDH19-variant individuals identifies psychiatric comorbidities, and association of seizure onset and disease severity
inferredcites →https://doi.org/10.1038/s41398-020-0803-0openalex-snapshot
A standardized patient-centered characterization of the phenotypic spectrum of PCDH19 girls clustering epilepsy
inferredcites →https://doi.org/10.1046/j.1528-1157.2001.042007837.xopenalex-snapshot
Severe Myoclonic Epilepsy of Infancy: Extended Spectrum of GEFS+?
inferredcites →https://doi.org/10.1046/j.1528-1157.2003.05302.xopenalex-snapshot
Seizure Characterization and Electroencephalographic Features in Glut‐1 Deficiency Syndrome
inferredcites →https://doi.org/10.1053/seiz.2001.0629openalex-snapshot
Prophylactic antiepileptic treatment in Sturge–Weber disease
inferredcites →https://doi.org/10.1055/s-0037-1621721openalex-snapshot
Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings
inferredcites →https://doi.org/10.1055/s-2008-1059590openalex-snapshot
A Long-term Follow-up Study of 214 Children with the Syndrome of Infantile Spasms
inferredcites →https://doi.org/10.1056/nejm199109053251006openalex-snapshot
Defective Glucose Transport across the Blood-Brain Barrier as a Cause of Persistent Hypoglycorrhachia, Seizures, and Developmental Delay
inferredcites →https://doi.org/10.1056/nejmc1714579openalex-snapshot
Parental Mosaicism in “De Novo” Epileptic Encephalopathies
inferredcites →https://doi.org/10.1056/nejmoa1213507openalex-snapshot
Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
inferredcites →https://doi.org/10.1073/pnas.211431298openalex-snapshot
Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K + channel
inferredcites →https://doi.org/10.1086/514877openalex-snapshot
Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16
inferredcites →https://doi.org/10.1093/brain/120.3.479openalex-snapshot
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
inferredcites →https://doi.org/10.1093/brain/awab162openalex-snapshot
Early childhood epilepsies: epidemiology, classification, aetiology, and socio-economic determinants
inferredcites →https://doi.org/10.1093/brain/awl272openalex-snapshot
Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations
inferredcites →https://doi.org/10.1093/brain/awm338openalex-snapshot
Epilepsy and mental retardation limited to females: an under-recognized disorder
inferredcites →https://doi.org/10.1093/brain/awn197openalex-snapshot
Key clinical features to identify girls with CDKL5 mutations
inferredcites →https://doi.org/10.1093/brain/awp336openalex-snapshot
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder
inferredcites →https://doi.org/10.1093/brain/awq143openalex-snapshot
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)
inferredcites →https://doi.org/10.1093/brain/aws151openalex-snapshot
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
inferredcites →https://doi.org/10.1093/brain/awt073openalex-snapshot
Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum
inferredcites →https://doi.org/10.1093/brain/awu051openalex-snapshot
Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcome
inferredcites →https://doi.org/10.1093/brain/aww302openalex-snapshot
Longitudinal course of epilepsy in Rett syndrome and related disorders
inferredcites →https://doi.org/10.1093/brain/awx054openalex-snapshot
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
inferredcites →https://doi.org/10.1093/brain/awz195openalex-snapshot
Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort
inferredcites →https://doi.org/10.1093/brain/awz240openalex-snapshot
KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEP
inferredcites →https://doi.org/10.1093/hmg/ddi120openalex-snapshot
Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5′-phosphate oxidase
inferredcites →https://doi.org/10.1097/00004691-199007000-00005openalex-snapshot
Early Myoclonic Encephalopathy, Early Infantile Epileptic Encephalopathy, and Benign and Severe Infantile Myoclonic Epilepsies
inferredcites →https://doi.org/10.1097/00004691-200311000-00003openalex-snapshot
Epileptic Encephalopathies in Early Infancy With Suppression-Burst
inferredcites →https://doi.org/10.1097/00004691-200311000-00005openalex-snapshot
Lennox-Gastaut Syndrome (Childhood Epileptic Encephalopathy)
inferredcites →https://doi.org/10.1097/00005072-199307000-00012openalex-snapshot
Epileptic Syndromes in Infancy, Childhood and Adolescence
inferredcites →https://doi.org/10.1097/wnp.0000000000000178openalex-snapshot
Characteristic Features of the Interictal EEG Background in 2 Patients With Malignant Migrating Partial Epilepsy in Infancy
inferredcites →https://doi.org/10.1111/ane.12902openalex-snapshot
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)
inferredcites →https://doi.org/10.1111/bjd.13203openalex-snapshot
New vascular classification of port‐wine stains: improving prediction of Sturge–Weber risk
inferredcites →https://doi.org/10.1111/dmcn.12593openalex-snapshot
Lamotrigine can be beneficial in patients with Dravet syndrome
inferredcites →https://doi.org/10.1111/dmcn.13141openalex-snapshot
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy
inferredcites →https://doi.org/10.1111/dmcn.14253openalex-snapshot
Early magnetic resonance imaging to detect presymptomatic leptomeningeal angioma in children with suspected Sturge–Weber syndrome
inferredcites →https://doi.org/10.1111/dmcn.14385openalex-snapshot
Clinical and genetic features in pyridoxine‐dependent epilepsy: a Chinese cohort study
inferredcites →https://doi.org/10.1111/epi.12007openalex-snapshot
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency
inferredcites →https://doi.org/10.1111/epi.12046openalex-snapshot
A population‐based study of newly diagnosed epilepsy in infants
inferredcites →https://doi.org/10.1111/epi.12089openalex-snapshot
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance
inferredcites →https://doi.org/10.1111/epi.12200openalex-snapshot
Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation
inferredcites →https://doi.org/10.1111/epi.12256openalex-snapshot
Dravet syndrome: New potential genetic modifiers, imaging abnormalities, and ictal findings
inferredcites →https://doi.org/10.1111/epi.12715openalex-snapshot
The variable phenotypes of KCNQ ‐related epilepsy
inferredcites →https://doi.org/10.1111/epi.12984openalex-snapshot
Early and effective treatment of KCNQ 2 encephalopathy
inferredcites →https://doi.org/10.1111/epi.13020openalex-snapshot
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
inferredcites →https://doi.org/10.1111/epi.13071openalex-snapshot
Mutations in KCNT 1 cause a spectrum of focal epilepsies
inferredcites →https://doi.org/10.1111/epi.13072openalex-snapshot
De novo KCNT 1 mutations in early‐onset epileptic encephalopathy
inferredcites →https://doi.org/10.1111/epi.13221openalex-snapshot
Surgical treatment for refractory epileptic spasms: The Detroit series
inferredcites →https://doi.org/10.1111/epi.13596openalex-snapshot
Rapid and safe response to low‐dose carbamazepine in neonatal epilepsy
inferredcites →https://doi.org/10.1111/epi.13649openalex-snapshot
De novo SCN 1A pathogenic variants in the GEFS + spectrum: Not always a familial syndrome
inferredcites →https://doi.org/10.1111/epi.13669openalex-snapshot
Heterozygous truncation mutations of the SMC 1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases
inferredcites →https://doi.org/10.1111/epi.13709openalex-snapshot
ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology
inferredcites →https://doi.org/10.1111/epi.13889openalex-snapshot
Dravet syndrome and its mimics: Beyond SCN 1A
inferredcites →https://doi.org/10.1111/epi.14074openalex-snapshot
Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders
inferredcites →https://doi.org/10.1111/epi.14600openalex-snapshot
Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study
inferredcites →https://doi.org/10.1111/epi.14605openalex-snapshot
Quantitative analysis and EEG markers of KCNT 1 epilepsy of infancy with migrating focal seizures
inferredcites →https://doi.org/10.1111/epi.16285openalex-snapshot
CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development
inferredcites →https://doi.org/10.1111/epi.16314openalex-snapshot
Characteristics of KCNQ 2 variants causing either benign neonatal epilepsy or developmental and epileptic encephalopathy
inferredcites →https://doi.org/10.1111/epi.16386openalex-snapshot
SCN1A‐related phenotypes: Epilepsy and beyond
inferredcites →https://doi.org/10.1111/epi.16810openalex-snapshot
The severe epilepsy syndromes of infancy: A population‐based study
inferredcites →https://doi.org/10.1111/epi.16815openalex-snapshot
The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures
inferredcites →https://doi.org/10.1111/epi.16957openalex-snapshot
Neonatal presentation of genetic epilepsies: Early differentiation from acute provoked seizures
inferredcites →https://doi.org/10.1111/epi.17237openalex-snapshot
Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions
inferredcites →https://doi.org/10.1111/j.0013-9580.2004.02404.xopenalex-snapshot
A Proposal for Case Definitions and Outcome Measures in Studies of Infantile Spasms and West Syndrome: Consensus Statement of the West Delphi Group
inferredcites →https://doi.org/10.1111/j.0013-9580.2004.04303.xopenalex-snapshot
Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations
inferredcites →https://doi.org/10.1111/j.0013-9580.2005.34104.xopenalex-snapshot
Migrating Partial Seizures in Infancy: Expanding the Phenotype of a Rare Seizure Syndrome
inferredcites →https://doi.org/10.1111/j.1440-1819.1985.tb02013.xopenalex-snapshot
On the Proposal for Classification of Epilepsies and Epileptic Syndromes
inferredcites →https://doi.org/10.1111/j.1440-1819.1993.tb02050.xopenalex-snapshot
Early Infantile Epileptic Syndromes with Suppression‐Bursts: Early Myoclonic Encephalopathy vs. Ohtahara Syndrome
inferredcites →https://doi.org/10.1111/j.1469-8749.2008.03091.xopenalex-snapshot
Malignant migrating partial seizures in Aicardi syndrome
inferredcites →https://doi.org/10.1111/j.1469-8749.2010.03889.xopenalex-snapshot
CDKL5 gene‐related epileptic encephalopathy: electroclinical findings in the first year of life
inferredcites →https://doi.org/10.1111/j.1469-8749.2012.04347.xopenalex-snapshot
Long‐term outcome in pyridoxine‐dependent epilepsy
inferredcites →https://doi.org/10.1111/j.1528-1157.1985.tb05417.xopenalex-snapshot
Proposal for Classification of Epilepsies and Epileptic Syndromes
inferredcites →https://doi.org/10.1111/j.1528-1157.1993.tb00445.xopenalex-snapshot
Ictal Clinical Electroencephalographic Findings of Spasms in West Syndrome
inferredcites →https://doi.org/10.1111/j.1528-1157.1993.tb02586.xopenalex-snapshot
Incidence of Epilepsy and Unprovoked Seizures in Rochester, Minnesota: 1935–1984
inferredcites →https://doi.org/10.1111/j.1528-1157.1995.tb00961.xopenalex-snapshot
Migrating Partial Seizures in Infancy: A Malignant Disorder with Developmental Arrest
inferredcites →https://doi.org/10.1111/j.1528-1157.1996.tb00506.xopenalex-snapshot
Incidence of Epilepsy in Childhood and Adolescence: A Population‐Based Study in Nova Scotia from 1977 to 1985
inferredcites →https://doi.org/10.1111/j.1528-1157.1997.tb00065.xopenalex-snapshot
Prevalence and Descriptive Epidemiology of Lennox‐Gastaut Syndrome Among Atlanta Children
inferredcites →https://doi.org/10.1111/j.1528-1157.1997.tb01136.xopenalex-snapshot
Community‐Based Study of Lennox‐Gastaut Syndrome
inferredcites →https://doi.org/10.1111/j.1528-1157.1999.tb00705.xopenalex-snapshot
Occurrence, Outcome, and Prognostic Factors of Infantile Spasms and Lennox‐Gastaut Syndrome
inferredcites →https://doi.org/10.1111/j.1528-1157.1999.tb01997.xopenalex-snapshot
Benign Familial Neonatal Convulsions Followed by Benign Epilepsy with Centrotemporal Spikes in Two Siblings
inferredcites →https://doi.org/10.1111/j.1528-1157.2000.tb02210.xopenalex-snapshot
Severe Myoclonic Epilepsy in Infants and its Related Syndromes
inferredcites →https://doi.org/10.1111/j.1528-1167.2006.00381.xopenalex-snapshot
Cognitive Functions in Juvenile and Adult Patients with Gelastic Epilepsy due to Hypothalamic Hamartoma
inferredcites →https://doi.org/10.1111/j.1528-1167.2006.00433.xopenalex-snapshot
Benign Myoclonic Epilepsy in Infants: Electroclinical Features and Long‐term Follow‐up of 34 Patients
inferredcites →https://doi.org/10.1111/j.1528-1167.2006.00688.xopenalex-snapshot
Severe Myoclonic Epilepsy of Infants (Dravet Syndrome): Natural History and Neuropsychological Findings
inferredcites →https://doi.org/10.1111/j.1528-1167.2006.00835.xopenalex-snapshot
Hypothalamic Hamartoma and Infantile Spasms
inferredcites →https://doi.org/10.1111/j.1528-1167.2007.01049.xopenalex-snapshot
SCN2A Mutations and Benign Familial Neonatal‐Infantile Seizures: The Phenotypic Spectrum
inferredcites →https://doi.org/10.1111/j.1528-1167.2007.01461.xopenalex-snapshot
Global cognitive function in children with epilepsy: A community‐based study
inferredcites →https://doi.org/10.1111/j.1528-1167.2007.01520.xopenalex-snapshot
The three stages of epilepsy in patients with CDKL5 mutations
inferredcites →https://doi.org/10.1111/j.1528-1167.2008.01816.xopenalex-snapshot
Prevalence of ALDH7A1 mutations in 18 North American pyridoxine‐dependent seizure (PDS) patients
inferredcites →https://doi.org/10.1111/j.1528-1167.2009.02121.xopenalex-snapshot
Malignant migrating partial seizures in infancy: An epilepsy syndrome of unknown etiology
inferredcites →https://doi.org/10.1111/j.1528-1167.2010.02522.xopenalex-snapshot
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009
inferredcites →https://doi.org/10.1111/j.1528-1167.2010.02695.xopenalex-snapshot
The underlying etiology of infantile spasms (West syndrome): Information from the United Kingdom Infantile Spasms Study (UKISS) on contemporary causes and their classification2
inferredcites →https://doi.org/10.1111/j.1528-1167.2011.02998.xopenalex-snapshot
Neuroimaging and neuropathology of Dravet syndrome
inferredcites →https://doi.org/10.1111/j.1528-1167.2011.03001.xopenalex-snapshot
Dravet syndrome: The long‐term outcome
inferredcites →https://doi.org/10.1111/j.1528-1167.2011.03127.xopenalex-snapshot
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
inferredcites →https://doi.org/10.1111/j.1528-1167.2011.03181.xopenalex-snapshot
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations
inferredcites →https://doi.org/10.1111/j.1528-1167.2012.03562.xopenalex-snapshot
Predictors and course of medically intractable epilepsy in young children presenting before 36 months of age: A retrospective, population‐based study
inferredcites →https://doi.org/10.1111/j.1528-1167.2012.03592.xopenalex-snapshot
Glucose transporter type I deficiency syndrome: Epilepsy phenotypes and outcomes
inferredcites →https://doi.org/10.1111/j.1528-1167.2012.03632.xopenalex-snapshot
Developmental outcomes of childhood‐onset temporal lobe epilepsy: A community‐based study
inferredcites →https://doi.org/10.1126/science.279.5349.403openalex-snapshot
A Potassium Channel Mutation in Neonatal Human Epilepsy
inferredcites →https://doi.org/10.1136/adc.74.1.19openalex-snapshot
Benign partial epilepsy in infancy.
inferredcites →https://doi.org/10.1136/adc.81.5.431openalex-snapshot
Epidemiology of pyridoxine dependent and pyridoxine responsive seizures in the UK
inferredcites →https://doi.org/10.1136/jmedgenet-2012-101406openalex-snapshot
Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy
inferredcites →https://doi.org/10.1136/jmedgenet-2018-105288openalex-snapshot
PEHO syndrome: the endpoint of different genetic epilepsies
inferredcites →https://doi.org/10.1136/jmg.2007.051938openalex-snapshot
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures
inferredcites →https://doi.org/10.1177/08830738030180041201openalex-snapshot
Magnetic Resonance Imaging Findings in Infantile Spasms: Etiologic and Pathophysiologic Aspects
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Peri‐ictal EEG in infants with PRRT2‐related self‐limited infantile epilepsy
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Late infantile epileptic encephalopathy: A distinct developmental and epileptic encephalopathy syndrome
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KCNJ11 ‐associated infantile epileptic spasms syndrome and neonatal diabetes
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Efficacy of fenfluramine in a pediatric epilepsy patient with a pathogenic SV2A variant: A case report
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Functional (dissociative) seizures in PCDH19 ‐clustering epilepsy: Clinical characteristics and diagnostic challenges
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Evolution from reflex myoclonic epilepsy of infancy to childhood absence epilepsy in NRXN1 ‐related disorder
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Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants
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Spindle density relates to cognitive outcomes in infantile epileptic spasms syndrome with unknown etiology: A retrospective cohort study
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Underutilization of syndrome‐specific ICD ‐10 codes for genetic epilepsies: Implications for precision medicine
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Progress report on new epilepsy treatments: A summary of the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices ( EILAT XVIII ). II . Treatments in more advanced clinical development
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Insights into ANKRD11 ‐related epilepsy from 163 people
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Prolonged fenfluramine use in open‐label studies of Dravet or Lennox–Gastaut syndromes: Long‐term safety, tolerability, patient global functioning, and considerations for interpreting effectiveness
inferred← citeshttps://doi.org/10.1002/epi.70391openalex-snapshot
Comorbidity spectrum in children and youth with epilepsy based on a validated and classified population‐based childhood epilepsy cohort
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Introducing the D‐ DAND scale: Development of a comprehensive caregiver‐administered tool for Dravet syndrome comorbidities
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How should etiology change the classification of the epilepsies? Report from the ILAE 2021–2025 Terminology Commission
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Phenotypic and transcriptomic characterization of biallelic RNU2‐2 developmental and epileptic encephalopathy
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Characterizing sleep disturbances in developmental and epileptic encephalopathies through natural language processing: A retrospective monocentric study
inferred← citeshttps://doi.org/10.1002/epi.70543openalex-snapshot
Longitudinal developmental trajectories after epilepsy surgery in early childhood: A biphasic developmental hypothesis
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Efficacy of vigabatrin in the treatment of infantile epileptic spasms syndrome: A systematic review and meta‐analysis
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Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
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PRRT2 ‐positive self‐limited infantile epilepsy: Initial seizure characteristics and response to sodium channel blockers
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Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
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Seizure features and outcomes in 50 children with GATOR1 variants: A retrospective study, more favorable for epilepsy surgery
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Vaccination against COVID ‐19 and potential protective effects on seizure recurrence in children with epilepsy: A cross‐sectional survey
inferred← citeshttps://doi.org/10.1002/epi4.12799openalex-snapshot
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome
inferred← citeshttps://doi.org/10.1002/epi4.12811openalex-snapshot
Landscape of genetic infantile epileptic spasms syndrome—A multicenter cohort of 124 children from India
inferred← citeshttps://doi.org/10.1002/epi4.12824openalex-snapshot
First report of Tunisian patients with CDKL5‐related encephalopathy
inferred← citeshttps://doi.org/10.1002/epi4.12827openalex-snapshot
Scalp high‐frequency oscillations differentiate neonates with seizures from healthy neonates
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EEG‐based spatiotemporal dynamics of fast ripple networks and hubs in infantile epileptic spasms
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Dravet syndrome: A systematic literature review of the illness burden
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Use of ketogenic dietary therapy for drug‐resistant epilepsy in early infancy
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Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy
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Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report
inferred← citeshttps://doi.org/10.1002/epi4.12899openalex-snapshot
Long‐term effectiveness and tolerability of ketogenic diet therapy in patients with genetic developmental and epileptic encephalopathy onset within the first 6 months of life
inferred← citeshttps://doi.org/10.1002/epi4.12908openalex-snapshot
Norwegian population‐based study of effectiveness of vagus nerve stimulation in patients with developmental and epileptic encephalopathies
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Providing quality care for people with CDKL5 deficiency disorder: A European expert panel opinion on the patient journey
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Myoclonus: Differential diagnosis and current management
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Consensus panel recommendations for the optimization of EPIDIOLEX® treatment for seizures associated with Lennox–Gastaut syndrome, Dravet syndrome, and tuberous sclerosis complex
inferred← citeshttps://doi.org/10.1002/epi4.12966openalex-snapshot
Epilepsies with onset during the first year of life: A prospective study on syndromes, etiologies, and outcomes
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Efficacy of anti‐seizure medications and alternative therapies (ketogenic diet, CBD, and quinidine) in KCNT1‐related epilepsy: A systematic review
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Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox–Gastaut syndrome in clinical practice
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The thickness of the retinal nerve fiber layer, macula, and ganglion cell‐inner plexiform layer in people with drug‐resistant epilepsy
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Clinical and genetic analysis of 23 Chinese children with epilepsy associated with KCNQ2 gene mutations
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The long odyssey for the DEE‐CDKL5 diagnosis: A call for action
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First‐choice hormonal therapies for children with infantile epileptic spasms syndrome in South Asia: A network meta‐analysis of randomized controlled trials
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Defining neonatal status epilepticus: A scoping review from the ILAE neonatal task force
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Antiseizure medication prescribing in people with Dravet syndrome: An analysis of real‐time administrative data
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Exome sequencing in Nigerian children with early‐onset epilepsy syndromes
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Inherited metabolic epilepsies–established diseases, new approaches
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Communicating a diagnosis of Dravet syndrome to parents/caregivers: An international Delphi consensus
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Disparities in the utilization of genetic testing for non‐acquired infantile epileptic spasms syndrome in a single healthcare center in North Carolina
inferred← citeshttps://doi.org/10.1002/epi4.70022openalex-snapshot
Comparative assessment of artificial intelligence chatbots' performance in responding to healthcare professionals' and caregivers' questions about Dravet syndrome
inferred← citeshttps://doi.org/10.1002/epi4.70034openalex-snapshot
Decreased homovanillic acid and 5‐hydroxyindoleacetic acid levels in the cerebrospinal fluid of patients with Dravet syndrome with parkinsonism
inferred← citeshttps://doi.org/10.1002/epi4.70039openalex-snapshot
Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes
inferred← citeshttps://doi.org/10.1002/epi4.70042openalex-snapshot
New insights into epileptic spasm generation and treatment from the TTX animal model
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Neonatal seizures: Advances in diagnosis and management
inferred← citeshttps://doi.org/10.1002/epi4.70116openalex-snapshot
Frontiers in EEG as a tool for the management of pediatric epilepsy: Past, present, and future
inferred← citeshttps://doi.org/10.1002/epi4.70126openalex-snapshot
Long‐term outcomes of a cohort of patients with pharmacoresistant neonatal epilepsy and negative brain MRI
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Epileptic drop attacks: More than just atonic seizures
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Prenatal betamethasone–postnatal N‐methyl‐D‐aspartic acid model of spasms: Update on mechanisms and treatments
inferred← citeshttps://doi.org/10.1002/epi4.70154openalex-snapshot
To the editors: SCN1A gain‐of‐function effects in Dravet syndrome: Insights into clinical phenotypes and therapeutic implications
inferred← citeshttps://doi.org/10.1002/epi4.70158openalex-snapshot
The multiple hit model of infantile and epileptic spasms: The 2025 update
inferred← citeshttps://doi.org/10.1002/epi4.70168openalex-snapshot
Ketogenic diet for infantile epileptic spasms
inferred← citeshttps://doi.org/10.1002/epi4.70191openalex-snapshot
Stiripentol use in Dravet syndrome patients in the USA : Results of a real‐world study
inferred← citeshttps://doi.org/10.1002/epi4.70197openalex-snapshot
Prevalence and incidence of infantile epileptic spasms syndrome in India: A systematic review and meta‐analysis
inferred← citeshttps://doi.org/10.1002/epi4.70207openalex-snapshot
Incidence and clinical predictors of epilepsy after febrile seizures in children: A prospective cohort study in Vietnam
inferred← citeshttps://doi.org/10.1002/epi4.70208openalex-snapshot
Distinctive genetic architecture of infantile epileptic spasms syndrome compared to self‐limited infantile epilepsy by trios whole‐exome sequencing
inferred← citeshttps://doi.org/10.1002/epi4.70266openalex-snapshot
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity
inferred← citeshttps://doi.org/10.1002/epi4.70278openalex-snapshot
Fast sleep spindles as a potential prognostic marker of developmental outcome in infantile epileptic spasms syndrome
inferred← citeshttps://doi.org/10.1002/epi4.70289openalex-snapshot
Cannabidiol reduces atypical absence seizures and epileptic spasms in a Gabrb3 +/D120N mouse model of Lennox–Gastaut syndrome
inferred← citeshttps://doi.org/10.1002/epi4.70292openalex-snapshot
Smartphone videos for infantile epileptic spasms triaging and assessment ( VISTA study): Impact of education and standardized clinical history on diagnostic accuracy
inferred← citeshttps://doi.org/10.1002/epi4.70305openalex-snapshot
Complete lesion resection and early surgical intervention are favorable factors for long‐term seizure freedom in drug‐resistant epileptic spasms
inferred← citeshttps://doi.org/10.1002/epi4.70309openalex-snapshot
Management of Infantile Epileptic Spasms Syndrome: A survey of US pediatric hospitals
inferred← citeshttps://doi.org/10.1002/epi4.70319openalex-snapshot
Long‐term developmental outcome in infantile epileptic spasms syndrome after high‐dose prednisolone and vigabatrin treatment
inferred← citeshttps://doi.org/10.1002/epi4.70328openalex-snapshot
From first seizure to specific antiseizure medication in Dravet syndrome: Quantifying delays in the DS ' coverED study
inferred← citeshttps://doi.org/10.1002/epi4.70338openalex-snapshot
Impact of vigabatrin on risk of relapse of infantile spasms
inferred← citeshttps://doi.org/10.1002/epi4.70347openalex-snapshot
Efficacy of stiripentol, fenfluramine, and their combination on clinical outcomes in Dravet syndrome: A preliminary report
inferred← citeshttps://doi.org/10.1002/jdn.10309openalex-snapshot
Infantile epileptic spasm syndrome as a new NR2F1 gene phenotype
inferred← citeshttps://doi.org/10.1002/jdn.70154openalex-snapshot
The Bright Side of the Spectrum: Self‐Limited Infantile Epilepsy‐Related SCN8A Gof Variant
inferred← citeshttps://doi.org/10.1002/mdc3.70414openalex-snapshot
ACTH ‐Induced Dyskinesia Mimics Autoimmune Encephalitis: A Case Report with Literature Review
inferred← citeshttps://doi.org/10.1002/pdi3.59openalex-snapshot
Benign convulsions with mild gastroenteritis in children: An emerging acute symptomatic seizures
inferred← citeshttps://doi.org/10.1007/978-3-031-77741-7_1openalex-snapshot
Classification of Seizures and Epilepsy
inferred← citeshttps://doi.org/10.1007/978-3-031-77741-7_2openalex-snapshot
Seizures and Epilepsy Syndromes
inferred← citeshttps://doi.org/10.1007/978-3-662-63267-3_23openalex-snapshot
EEG in der Neuropädiatrie
inferred← citeshttps://doi.org/10.1007/978-3-662-72532-0_6openalex-snapshot
Symptomatik der Enzephalopathien
inferred← citeshttps://doi.org/10.1007/978-981-96-8520-2_3openalex-snapshot
The Basic Principles and Precautions of Drug Therapy
inferred← citeshttps://doi.org/10.1007/978-981-96-8520-2_5openalex-snapshot
Diagnosis and Treatment of Epilepsy Syndromes
inferred← citeshttps://doi.org/10.1007/s00381-025-06879-1openalex-snapshot
Effectiveness of vagus nerve stimulation in Dravet syndrome: a case series
inferred← citeshttps://doi.org/10.1007/s00415-024-12352-xopenalex-snapshot
Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights
inferred← citeshttps://doi.org/10.1007/s00415-025-13135-8openalex-snapshot
Fenfluramine: an effective treatment for developmental epileptic encephalopathies beyond Dravet and Lennox–Gastaut Syndromes
inferred← citeshttps://doi.org/10.1007/s00415-025-13454-wopenalex-snapshot
Risk factors of recurrence for epilepsy patients after antiseizure medication withdrawal: what we do and do not know?
inferred← citeshttps://doi.org/10.1007/s00415-025-13544-9openalex-snapshot
Clinical and genetics spectrum of 392 Chinese patients with genetic epilepsy with febrile seizures plus
inferred← citeshttps://doi.org/10.1007/s10048-025-00850-7openalex-snapshot
Bridging the gap: pyridoxine-dependent epilepsy (PDE-ALDH7A1) diagnosis and management in a low-resource setting
inferred← citeshttps://doi.org/10.1007/s10072-023-07078-zopenalex-snapshot
Treatment modalities for infantile spasms: current considerations and evolving strategies in clinical practice
inferred← citeshttps://doi.org/10.1007/s10072-024-07783-3openalex-snapshot
Early mortality in STXBP1-related disorders
inferred← citeshttps://doi.org/10.1007/s10072-026-08868-xopenalex-snapshot
The impact of vagus nerve stimulation on the most disabling seizures: A retrospective study in adults with drug-resistant epilepsy
inferred← citeshttps://doi.org/10.1007/s10072-026-08936-2openalex-snapshot
Heterogeneity of monogenic epilepsy in loci, phenotypes, and treatment approaches
inferred← citeshttps://doi.org/10.1007/s10072-026-09036-xopenalex-snapshot
Clinical spectrum and treatment responses in
inferred← citeshttps://doi.org/10.1007/s10072-026-09227-6openalex-snapshot
Risk of epilepsy in people with adult-onset hydrocephalus: insights from the UK Biobank
inferred← citeshttps://doi.org/10.1007/s10143-024-02912-0openalex-snapshot
RETRACTED ARTICLE: Transforming neurosurgical approaches to Aicardi syndrome through Artificial Intelligence
inferred← citeshttps://doi.org/10.1007/s10309-022-00534-4openalex-snapshot
Neonatal seizures—diagnostic options and treatment recommendations
inferred← citeshttps://doi.org/10.1007/s10309-023-00568-2openalex-snapshot
Genetics of nonlesional focal epilepsy in adults and surgical implications
inferred← citeshttps://doi.org/10.1007/s10309-023-00572-6openalex-snapshot
Nichtläsionelle Epilepsie im Kindesalter – Fallstricke in der Diagnostik
inferred← citeshttps://doi.org/10.1007/s10309-023-00646-5openalex-snapshot
Fenfluramine in clinical practice: new therapy option for Dravet and Lennox–Gastaut syndromes
inferred← citeshttps://doi.org/10.1007/s10309-024-00720-6openalex-snapshot
Sleep-related epilepsies in the course of development in childhood
inferred← citeshttps://doi.org/10.1007/s10309-025-00772-2openalex-snapshot
Neonatale Entwicklungs- und epileptische Enzephalopathien
inferred← citeshttps://doi.org/10.1007/s10309-025-00788-8openalex-snapshot
Anfallszunahme beim SCN1A-assoziierten Dravet-Syndrom unter Cenobamat: Fallserie und Literaturübersicht
inferred← citeshttps://doi.org/10.1007/s10309-025-00789-7openalex-snapshot
Revidierte Klassifikation epileptischer Anfälle: Positionspapier der Internationalen Liga gegen Epilepsie
inferred← citeshttps://doi.org/10.1007/s10309-025-00790-0openalex-snapshot
Revision der ILAE(International League Against Epilepsy)-Anfallsklassifikation 2025
inferred← citeshttps://doi.org/10.1007/s10309-025-00805-wopenalex-snapshot
Neonatal developmental and epileptic encephalopathies. English version
inferred← citeshttps://doi.org/10.1007/s10309-025-00808-7openalex-snapshot
Seizure worsening in SCN1A-associated Dravet syndrome while on cenobamate: case series and literature review. English version
inferred← citeshttps://doi.org/10.1007/s10309-026-00849-6openalex-snapshot
Genetik frühkindlicher Epilepsien und epileptischer Syndrome
inferred← citeshttps://doi.org/10.1007/s10309-026-00850-zopenalex-snapshot
EEG in the diagnosis and management of early childhood epilepsies
inferred← citeshttps://doi.org/10.1007/s10309-026-00855-8openalex-snapshot
Einführung: Frühkindliche Epilepsien und epileptische Syndrome
inferred← citeshttps://doi.org/10.1007/s11033-026-12609-wopenalex-snapshot
A de novo NR2F1 c.330 C > A variant in Bosch-Boonstra-Schaaf optic atrophy syndrome presenting with early-onset developmental and epileptic encephalopathy
inferred← citeshttps://doi.org/10.1007/s11055-025-01823-xopenalex-snapshot
Molecular Genetic Causes of Epilepsy in Children
inferred← citeshttps://doi.org/10.1007/s11064-024-04300-yopenalex-snapshot
ALG13-Related Epilepsy: Current Insights and Future Research Directions
inferred← citeshttps://doi.org/10.1007/s11064-025-04471-2openalex-snapshot
Emerging Insights into the Pathogenic Mechanisms of Dravet Syndrome
inferred← citeshttps://doi.org/10.1007/s11517-025-03295-0openalex-snapshot
Graph convolution network-based eeg signal analysis: a review
inferred← citeshttps://doi.org/10.1007/s11910-025-01413-xopenalex-snapshot
Monogenic Epilepsies in Adult Epilepsy Clinics and Gene-Driven Approaches to Treatment
inferred← citeshttps://doi.org/10.1007/s11910-025-01453-3openalex-snapshot
Pathophysiological Mechanisms Fostering Developmental and Epileptic Encephalopathies (DEE): a Complex Interplay between Genetics, Inflammation and Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s11940-026-00862-0openalex-snapshot
Update on Diagnosis and Treatment of Infantile Epileptic Spasms Syndrome and Developmental and Epileptic Encephalopathy with Spike Wave Activation in Sleep
inferred← citeshttps://doi.org/10.1007/s11940-026-00873-xopenalex-snapshot
Targeted Treatments for Genetic Epilepsies, Part 1: Channelopathies
inferred← citeshttps://doi.org/10.1007/s12098-023-05017-6openalex-snapshot
Electroclinical Landscape of Infantile Epileptic Spasms Syndrome
inferred← citeshttps://doi.org/10.1007/s12098-024-05308-6openalex-snapshot
Developmental and Epileptic Encephalopathies: Need for Bridging the Gaps Between Clinical Syndromes and Underlying Genetic Etiologies
inferred← citeshttps://doi.org/10.1007/s12098-024-05327-3openalex-snapshot
Infantile-Onset Epilepsies: Steering Towards New Horizons
inferred← citeshttps://doi.org/10.1007/s12098-024-05332-6openalex-snapshot
Short-Term Effectiveness and Tolerability of Vigabatrin Therapy in Infantile Epileptic Spasms Syndrome
inferred← citeshttps://doi.org/10.1007/s12204-024-2771-7openalex-snapshot
Mixture of Expert System for IESS Detection Based on EEG Signal
inferred← citeshttps://doi.org/10.1007/s12325-024-02813-0openalex-snapshot
An Update on Stiripentol Mechanisms of Action: A Narrative Review
inferred← citeshttps://doi.org/10.1007/s12519-022-00583-9openalex-snapshot
Integration of multiscale entropy and BASED scale of electroencephalography after adrenocorticotropic hormone therapy predict relapse of infantile spasms
inferred← citeshttps://doi.org/10.1007/s12519-024-00809-yopenalex-snapshot
Sturge–Weber syndrome: an update for the pediatrician
inferred← citeshttps://doi.org/10.1007/s13311-022-01264-1openalex-snapshot
Impact of Genetic Testing on Therapeutic Decision-Making in Childhood-Onset Epilepsies—a Study in a Tertiary Epilepsy Center
inferred← citeshttps://doi.org/10.1007/s13312-024-3115-2openalex-snapshot
The 2022 International League Against Epilepsy Classification and Definition of Childhood Epilepsy Syndromes: An Update for Pediatricians
inferred← citeshttps://doi.org/10.1007/s13312-025-00050-4openalex-snapshot
Advances in Neonatal Seizures (2024): An Update for Pediatricians
inferred← citeshttps://doi.org/10.1007/s13312-025-00061-1openalex-snapshot
Clinical Profile, Genotypes, and Outcomes in Children with Pyridoxine Dependent Epilepsy (PDE): A Single Center Experience from Southern India
inferred← citeshttps://doi.org/10.1007/s13760-024-02713-8openalex-snapshot
No single treatment modality exhibits clear superiority for infantile spasms syndrome: insights from a retrospective cohort study
inferred← citeshttps://doi.org/10.1007/s13760-025-02963-0openalex-snapshot
Infantile epileptic spasms syndrome associated with a PTEN variant
inferred← citeshttps://doi.org/10.1007/s40120-022-00412-1openalex-snapshot
Brain Complexity Predicts Response to Adrenocorticotropic Hormone in Infantile Epileptic Spasms Syndrome: A Retrospective Study
inferred← citeshttps://doi.org/10.1007/s40120-024-00677-8openalex-snapshot
Use of Stiripentol in Patients with Dravet Syndrome: Common Practice Among Experts in Spain
inferred← citeshttps://doi.org/10.1007/s40120-025-00713-1openalex-snapshot
Expert-Agreed Practical Recommendations on the Use of Fenfluramine in Developmental and Epileptic Encephalopathies Based on Clinical Experience and Literature Review
inferred← citeshttps://doi.org/10.1007/s40120-025-00722-0openalex-snapshot
Factors Influencing the Response of Patients with Infantile Epileptic Spasms Syndrome to ACTH as Repeated First-Line Therapy
inferred← citeshttps://doi.org/10.1007/s40120-025-00779-xopenalex-snapshot
Cenobamate for Adjunctive Treatment in Adult and Pediatric Patients with Refractory Lennox–Gastaut Syndrome: A Retrospective Chart Review
inferred← citeshttps://doi.org/10.1007/s40120-025-00788-wopenalex-snapshot
Retrospective Multicenter Chart Review Study of Adjunctive Cannabidiol for Seizures Associated with Lennox–Gastaut Syndrome, Dravet Syndrome and Tuberous Sclerosis Complex
inferred← citeshttps://doi.org/10.1007/s40120-025-00841-8openalex-snapshot
Short-Term Outcomes and Immunologic Mechanisms of Adrenocorticotropic Hormone in Infantile Epileptic Spasm Syndrome: A Multicenter Prospective Trial in Southern China
inferred← citeshttps://doi.org/10.1007/s40258-024-00886-0openalex-snapshot
Cost Effectiveness of Adding Fenfluramine to Standard of Care for Patients with Dravet Syndrome in Sweden
inferred← citeshttps://doi.org/10.1007/s40263-023-01025-4openalex-snapshot
New GABA-Targeting Therapies for the Treatment of Seizures and Epilepsy: II. Treatments in Clinical Development
inferred← citeshttps://doi.org/10.1007/s40263-023-01027-2openalex-snapshot
New GABA-Targeting Therapies for the Treatment of Seizures and Epilepsy: I. Role of GABA as a Modulator of Seizure Activity and Recently Approved Medications Acting on the GABA System
inferred← citeshttps://doi.org/10.1007/s40263-024-01149-1openalex-snapshot
Treatment of Seizures in People with Intellectual Disability
inferred← citeshttps://doi.org/10.1007/s40263-024-01155-3openalex-snapshot
Targeting Kv7 Potassium Channels for Epilepsy
inferred← citeshttps://doi.org/10.1007/s44326-024-00019-wopenalex-snapshot
Magnetic resonance imaging in pediatric epilepsy patients: two different protocols
inferred← citeshttps://doi.org/10.1007/s44443-026-00524-wopenalex-snapshot
MST-HGCN: A multimodal spatio-temporal hypergraph convolutional network for infantile spasms detection
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