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Effect of Cannabidiol on Drop Seizures in the Lennox–Gastaut Syndrome

The New England journal of medicine, 2018-05, Vol.378 (20), p.1888-1897

2018

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Dravet syndrome and its mimics: Beyond SCN1A

Epilepsia (Copenhagen), 2017-11, Vol.58 (11), p.1807-1816

2017

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Dravet syndrome—From epileptic encephalopathy to channelopathy

Epilepsia (Copenhagen), 2014-07, Vol.55 (7), p.979-984

2014

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Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology

Epilepsia (Copenhagen), 2017-04, Vol.58 (4), p.522-530

2017

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ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

Epilepsia (Copenhagen), 2017-04, Vol.58 (4), p.512-521

2017

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The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures

Epilepsia (Copenhagen), 2021-03, Vol.62 (3), p.615-628

2021

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Instruction manual for the ILAE 2017 operational classification of seizure types

Epilepsia (Copenhagen), 2017-04, Vol.58 (4), p.531-542

2017

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The burden of illness in Lennox-Gastaut syndrome: a systematic literature review

Orphanet journal of rare diseases, 2023-03, Vol.18 (1), p.42-42, Article 42

2023

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ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions

Epilepsia (Copenhagen), 2022-06, Vol.63 (6), p.1475-1499

2022

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Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort

Brain (London, England : 1878), 2019-08, Vol.142 (8), p.2303-2318

2019

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Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk

Epilepsia (Copenhagen), 2018-07, Vol.59 (7), p.1372-1380

2018

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Genotype phenotype associations across the voltage-gated sodium channel family

Journal of Medical Genetics, 2014-10, Vol.51 (10), p.650-658

2014

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Phenotypic spectrum and genetics of SCN2A‐related disorders, treatment options, and outcomes in epilepsy and beyond

Epilepsia (Copenhagen), 2019-12, Vol.60 (S3), p.S59-S67

2019

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

American journal of human genetics, 2012-01, Vol.90 (1), p.152-160

2012

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Outcome and prognostic features in opsoclonus-myoclonus syndrome from infancy to adult life

Pediatrics (Evanston), 2011-08, Vol.128 (2), p.e388-e394

2011

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ICD coding for epilepsy: Past, present, and future—A report by the International League Against Epilepsy Task Force on ICD codes in epilepsy

Epilepsia (Copenhagen), 2015-03, Vol.56 (3), p.348-355

2015

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Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe

Epilepsia open, 2022-03, Vol.7 (1), p.11-26

2022

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Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)

Brain (London, England : 1878), 2010-07, Vol.133 (7), p.2148-2159

2010

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Precision in child neurology: Networks, systems, and technology

Developmental medicine and child neurology, 2022-06, Vol.64 (6), p.673-673

Zuberi, Sameer M.

2022

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Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation

Pediatrics (Evanston), 2008-02, Vol.121 (2), p.404-410

2008

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An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real‐world practice setting: A report from the Fenfluramine European Early Access Program

Epilepsia open, 2022-12, Vol.7 (4), p.578-587

2022

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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

Epilepsia (Copenhagen), 2022-06, Vol.63 (6), p.1349-1397

2022

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International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions

Epilepsia (Copenhagen), 2022-06, Vol.63 (6), p.1398-1442

2022

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Classification of the epilepsies: New concepts for discussion and debate—Special report of the ILAE Classification Task Force of the Commission for Classification and Terminology

Epilepsia open, 2016-09, Vol.1 (1-2), p.37-44

2016

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Effect of Cannabidiol on Drop Seizures in the Lennox–Gastaut Syndrome

Dravet syndrome and its mimics: Beyond SCN1A

Dravet syndrome—From epileptic encephalopathy to channelopathy

Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures

Instruction manual for the ILAE 2017 operational classification of seizure types

The burden of illness in Lennox-Gastaut syndrome: a systematic literature review

ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions

Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort

Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk

Genotype phenotype associations across the voltage-gated sodium channel family

Phenotypic spectrum and genetics of SCN2A‐related disorders, treatment options, and outcomes in epilepsy and beyond

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Outcome and prognostic features in opsoclonus-myoclonus syndrome from infancy to adult life

ICD coding for epilepsy: Past, present, and future—A report by the International League Against Epilepsy Task Force on ICD codes in epilepsy

Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe

Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)

Precision in child neurology: Networks, systems, and technology

Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation

An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real‐world practice setting: A report from the Fenfluramine European Early Access Program

ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions

International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions

Classification of the epilepsies: New concepts for discussion and debate—Special report of the ILAE Classification Task Force of the Commission for Classification and Terminology

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