Research & Literature
Explore the leading researchers and institutions driving advances in this area, and dive into the full body of literature that informs this resource.
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Massachusetts General Hospital
Boston, United States
GW Pharmaceuticals (United Kingdom)
Cambridge, United Kingdom
NYU Langone Health
New York, United States
University of Alabama at Birmingham
Birmingham, United States
Northwestern University
Evanston, United States
Children's Hospital of Philadelphia
Philadelphia, United States
Great Ormond Street Hospital
London, United Kingdom
Royal Children's Hospital
Melbourne, Australia
Royal Hospital for Children
Glasgow, United Kingdom
The University of Sydney
Sydney, Australia
References
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Predictors of vagus nerve stimulation complications among pediatric patients with drug-resistant epilepsy.
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Paroxysmal fast activity is a biomarker of treatment response in deep brain stimulation for Lennox-Gastaut syndrome.
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Epilepsia 2022; (63(12)):3134-3147 doi:10.1111/epi.17414.
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Tonic Seizures in a Patient With Lennox-Gastaut Syndrome Manifest as "Icicles" Rather Than "Flames" on Quantitative EEG Analysis.
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Epileptogenesis in tuberous sclerosis complex-related developmental and epileptic encephalopathy.
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Efficacy and Safety of Fenfluramine in Epilepsy: A Systematic Review and Meta-analysis.
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Current and emerging pharmacotherapy for the treatment of Lennox-Gastaut syndrome.
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Proposed anti-seizure medication combinations with rufinamide in the treatment of Lennox-Gastaut syndrome: Narrative review and expert opinion.
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Seizure 2023; (110()):42-57 doi:10.1016/j.seizure.2023.05.018.
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Interrater reliability of interictal EEG waveforms in Lennox-Gastaut Syndrome.
Hu DK, Rana M, Adams DJ, et al.
Epilepsia open 2024; (9(1)):176-186 doi:10.1002/epi4.12858.
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Neurostimulation for Generalized Epilepsy: Should Therapy be Syndrome-specific?
Warren AEL, Tobochnik S, Chua MMJ, et al.
Neurosurgery clinics of North America 2024; (35(1)):27-48 doi:10.1016/j.nec.2023.08.001.
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Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort study.
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Epilepsia open 2024; (9(2)):602-612 doi:10.1002/epi4.12894.
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Long-term outcomes and adaptive behavior in adult patients with Lennox-Gastaut syndrome.
Cerulli Irelli E, Petrungaro A, Pastorino GMG, et al.
Epilepsia open 2024; (9(5)):1881-1890 doi:10.1002/epi4.13024.
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Comparative Analysis of Lennox-Gastaut Syndrome With Different Subtypes of Tonic Seizures: A Single-Center Retrospective Cohort Study.
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Pediatric neurology 2024; (161()):132-138 doi:10.1016/j.pediatrneurol.2024.07.018.
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Ketogenic diet therapy for epilepsy: Clinical pearls.
Pinto AL, Montenegro MA, Valente K, Sampaio LB
Epilepsy & behavior : E&B 2024; (161()):110091 doi:10.1016/j.yebeh.2024.110091.
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Discovering EEG biomarkers of Lennox-Gastaut syndrome through unsupervised time-frequency analysis.
Hu DK, Pinto-Orellana MA, Rana M, et al.
Epilepsia 2025; (66(2)):541-553 doi:10.1111/epi.18211.
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Understanding the Burden of Lennox-Gastaut Syndrome: Implications for Patients, Caregivers, and Society in High and Low Resource Settings: A Narrative Review.
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A Multicenter Retrospective Observational Cohort Study of Seizure Freedom before Lennox-Gastaut Syndrome (the "Gap"). Opportunities for Prevention.
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Neuromodulation Strategies in Lennox-Gastaut Syndrome: Practical Clinical Guidance from the Pediatric Epilepsy Research Consortium.
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Epilepsy research 2025; (210()):107499 doi:10.1016/j.eplepsyres.2024.107499.
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Antiseizure medications for Lennox-Gastaut Syndrome: Comprehensive review and proposed consensus treatment algorithm.
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Epilepsy & behavior : E&B 2025; (164()):110261 doi:10.1016/j.yebeh.2024.110261.
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Cognitive and behavioral impact of antiseizure medications, neuromodulation, ketogenic diet, and surgery in Lennox-Gastaut syndrome: A comprehensive review.
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Phenotypic Manifestations of a New Variant in HDAC4 Gene.
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American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2025; (198(6)):32-37 doi:10.1002/ajmg.b.33029.
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Current and emerging pharmacotherapies in Lennox-Gastaut syndrome.
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Neuropathologic Findings in Lennox-Gastaut Syndrome (SCN2A-Related): A Case Report and Review of Literature.
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Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2025; (28(5)):420-424 doi:10.1177/10935266251345684.
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Dysregulation of the Cannabinoid System in Childhood Epilepsy: From Mechanisms to Therapy.
Montebello G, Di Giovanni G
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A novel mutation in the DYNC1H1 gene causing developmental and epileptic encephalopathy treated with ketogenic diet: A case report.
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Medicine 2025; (104(28)):e43277 doi:10.1097/MD.0000000000043277.
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Navigating the Diagnosis: A survey on Caregivers' Journeys to Lennox-Gastaut Syndrome.
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Epilepsy & behavior : E&B 2025; (171()):110600 doi:10.1016/j.yebeh.2025.110600.
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Absence-Atonic Seizures: A Rare Generalized Seizure Type.
Ranpariya M, Hanson J, Qutab N, Farooq O
Journal of child neurology 2026; (41(3)):407-409 doi:10.1177/08830738251359388.
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Current practices and trends in surgical decision-making for children with Lennox-Gastaut syndrome: A cross-sectional survey by the Pediatric Epilepsy Research Consortium.
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Genetic Etiology of Developmental and Epileptic Encephalopathy in a Turkish Cohort: A Single-Center Study with Targeted Gene Panel and Whole Exome Sequencing.
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History of Lennox-Gastaut Syndrome: An electro-clinical voyage in search of an epileptic syndrome.
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Dietary therapies in Lennox-Gastaut syndrome.
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Late onset Lennox-Gastaut syndrome.
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Lennox-Gastaut syndrome: Comorbidities and clinical implications.
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Unraveling Lennox-Gastaut Syndrome: From Molecular Pathogenesis to Precision Diagnosis and Targeted Therapy Evolving Therapeutic Strategies.
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