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Outcomes of epilepsy surgery in adults and children

Lancet neurology, 2008-06, Vol.7 (6), p.525-537

2008

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Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

Epilepsia (Copenhagen), 2012-12, Vol.53 (12), p.e204-e207

2012

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Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy

American journal of human genetics, 2017-07, Vol.101 (1), p.65-74

2017

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Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy

Frontiers in neurology, 2019-05, Vol.10, p.434-434

2019

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Expanding the genotype-phenotype spectrum in SCN8A-related disorders

BMC neurology, 2024-01, Vol.24 (1), p.31-31, Article 31

2024

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De Novo Mutations in YWHAG Cause Early-Onset Epilepsy

American journal of human genetics, 2017-08, Vol.101 (2), p.300-310

2017

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Brivaracetam, but not ethosuximide, reverses memory impairments in an Alzheimer's disease mouse model

Alzheimer's research & therapy, 2015-05, Vol.7 (1), p.25-25, Article 25

2015

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Dosage Related Efficacy and Tolerability of Cannabidiol in Children With Treatment-Resistant Epileptic Encephalopathy: Preliminary Results of the CARE-E Study

Frontiers in neurology, 2019-07, Vol.10, p.716-716

2019

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The protocol for the Cannabidiol in children with refractory epileptic encephalopathy (CARE-E) study: a phase 1 dosage escalation study

BMC pediatrics, 2018-07, Vol.18 (1), p.221-9, Article 221

2018

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Neurological Prognostication After Hypoglycemic Coma: Role of Clinical and EEG Findings

Neurocritical care, 2022-08, Vol.37 (1), p.273-280

2022

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Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy

Molecular brain, 2019-11, Vol.12 (1), p.92-92, Article 92

2019

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Effect of Training on Visual Identification of High Frequency Oscillations-A Delphi-Style Intervention

Frontiers in neurology, 2022-02, Vol.13, p.794668-794668

2022

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Correction to: Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy

Molecular brain, 2020-03, Vol.13 (1), p.50-50, Article 50

2020

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Child Neurology: Pheochromocytoma Unveiled by Reversible Cerebral Vasoconstriction Syndrome in a Child With Neurofibromatosis Type 1

Neurology, 2021-01, Vol.96 (2), p.79-82

2021

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Developmental and epileptic encephalopathies after successful treatment of pediatric ALL: A case series and review of literature

Epileptic disorders, 2024-09

2024

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Sensitivity of quantitative EEG for seizure identification in the intensive care unit

Neurology, 2016-08, Vol.87 (9), p.935-944

2016

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Medicinal cannabis in children and adolescents with autism spectrum disorder: A scoping review

Child : care, health & development, 2022-01, Vol.48 (1), p.33-44

2022

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Rapid Implementation of Virtual Health in a Pediatric Neurology Practice During COVID-19

Canadian journal of neurological sciences, 2021-07, Vol.48 (4), p.575-577

2021

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SETD1B -associated neurodevelopmental disorder

Journal of medical genetics, 2021-03, Vol.58 (3), p.196-204

2021

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Three consecutive epilepsy syndromes in one child

Epileptic disorders, 2023-02, Vol.25 (1), p.114-116

2023

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Seizure action plans in the pediatric population with epilepsy: Uptake, determinants, and parental interest in a mobile application

Epilepsy & behavior, 2021-04, Vol.117, p.107860-107860, Article 107860

2021

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Clinical Experience With Perampanel for Refractory Pediatric Epilepsy in One Canadian Center

Journal of child neurology, 2017-08, Vol.32 (9), p.834-839

2017

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Outcomes of epilepsy surgery in adults and children

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy

Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy

Expanding the genotype-phenotype spectrum in SCN8A-related disorders

De Novo Mutations in YWHAG Cause Early-Onset Epilepsy

Brivaracetam, but not ethosuximide, reverses memory impairments in an Alzheimer's disease mouse model

Dosage Related Efficacy and Tolerability of Cannabidiol in Children With Treatment-Resistant Epileptic Encephalopathy: Preliminary Results of the CARE-E Study

Defining the phenotype of FHF1 developmental and epileptic encephalopathy

The protocol for the Cannabidiol in children with refractory epileptic encephalopathy (CARE-E) study: a phase 1 dosage escalation study

Neurological Prognostication After Hypoglycemic Coma: Role of Clinical and EEG Findings

Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy

Effect of Training on Visual Identification of High Frequency Oscillations-A Delphi-Style Intervention

Correction to: Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy

Child Neurology: Pheochromocytoma Unveiled by Reversible Cerebral Vasoconstriction Syndrome in a Child With Neurofibromatosis Type 1

A prospective study of loss of consciousness in epilepsy using virtual reality driving simulation and other video games

Developmental and epileptic encephalopathies after successful treatment of pediatric ALL: A case series and review of literature

Sensitivity of quantitative EEG for seizure identification in the intensive care unit

Medicinal cannabis in children and adolescents with autism spectrum disorder: A scoping review

Rapid Implementation of Virtual Health in a Pediatric Neurology Practice During COVID-19

SETD1B -associated neurodevelopmental disorder

Three consecutive epilepsy syndromes in one child

Seizure action plans in the pediatric population with epilepsy: Uptake, determinants, and parental interest in a mobile application

First-line medication dosing in pediatric refractory status epilepticus

Clinical Experience With Perampanel for Refractory Pediatric Epilepsy in One Canadian Center

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