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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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School performance in children at the time of new-onset seizures and at long-term follow-up: A retrospective cohort study

Journal of international medical research, 2022-04, Vol.50 (4), p.3000605221081032-3000605221081032

2022

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Resilience of adolescents and teenagers with self-limited and genetic-generalized epilepsy during the COVID-19 pandemic

Epilepsy & behavior reports, 2022-01, Vol.17, p.100520-100520, Article 100520

2022

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A video case vignette: Hypermotor activity, ictal aggression, and bolting in an adolescent with an anteromedial temporal lesion

Epileptic disorders, 2024-04, Vol.26 (2), p.236-239

Datta, Anita N.

2024

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Hypnagogic Frontal EEG Bursts in Children: Epileptic or Not?

Journal of clinical neurophysiology, 2021-11, Vol.38 (6), p.536-541

Datta, Anita N.

2021

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The impact of anti-seizure medications on psychiatric disorders among children with epilepsy: Both a challenge and an opportunity?

Journal of the Canadian Academy of Child and Adolescent Psychiatry, 2023-08, Vol.32 (3), p.177-184

Datta, Anita N

2023

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Clinical Presentation and Diagnosis of Tuberous Sclerosis Complex in Infancy

Journal of child neurology, 2008-03, Vol.23 (3), p.268-273

2008

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The Initial Experience of Eslicarbazepine in Children at Three Canadian Tertiary Pediatric Care Centers

Journal of child neurology, 2024-10, p.8830738241282903

2024

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Children With Trisomy 21 and Lennox-Gastaut Syndrome With Predominant Myoclonic Seizures

Journal of child neurology, 2021-10, Vol.36 (11), p.1027-1033

2021

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Original Research: Clinical Significance of a Unique Pediatric EEG Configuration: Bi-Frontal Spikes With Simultaneous Bi-Occipital Positivity

Clinical EEG and neuroscience, 2024-09, Vol.55 (5), p.591-600

2024

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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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Lack of response to quinidine in KCNT1‐related neonatal epilepsy

Epilepsia (Copenhagen), 2018-10, Vol.59 (10), p.1889-1898

2018

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Outcome of Absence Epilepsy With Onset at 8-11 Years of Age: Watershed Ages When Syndromes Overlap

Journal of child neurology, 2023-08, Vol.38 (8-9), p.505-512

2023

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Pediatric Occipital Spikes at a Single Center Over 26 Years and the Significance of Tangential Dipole

Journal of child neurology, 2021-06, Vol.36 (7), p.530-536

2021

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Infantile Spasms and Trisomy 21: Unfavorable Outcomes with First-line Vigabatrin Therapy

Canadian journal of neurological sciences, 2021-11, Vol.48 (6), p.839-844

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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Co-existence of Rolandic and 3 Hz Spike-Wave Discharges on EEG in Children with Epilepsy

Canadian journal of neurological sciences, 2019-01, Vol.46 (1), p.64-70

2019

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Predictive Value of Midline Spikes on Pediatric EEG for Seizure and Developmental Outcome

Journal of clinical neurophysiology, 2018-11, Vol.35 (6), p.490-495

2018

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Two Patients With KCNT1-Related Epilepsy Responding to Phenobarbital and Potassium Bromide

Journal of child neurology, 2019-10, Vol.34 (12), p.728-734

2019

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Clinical Significance of Incidental Rolandic Spikes in Children With Absence Epilepsy

Journal of child neurology, 2019-10, Vol.34 (11), p.631-638

2019

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Intelligence Quotient is Not Affected by Epilepsy Surgery in Childhood

Pediatric neurology, 2011-02, Vol.44 (2), p.117-121

2011

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Dipolar EEG Spikes Are More Benign

Journal of clinical neurophysiology, 2024-08

2024

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At What Point Should We Discontinue Treatment in Super-Refractory Status Epilepticus?

Journal of pediatric epilepsy, 2020-09, Vol.9 (3), p.100-101

Datta, Anita N.

2020

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Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5

Neurology, 2023-02, Vol.100 (6), p.e603

2023

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Lack of response to quinidine in KCNT 1 ‐related neonatal epilepsy

Epilepsia (Copenhagen), 2018-10, Vol.59 (10), p.1889-1898

2018

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Three consecutive epilepsy syndromes in one child

School performance in children at the time of new-onset seizures and at long-term follow-up: A retrospective cohort study

Resilience of adolescents and teenagers with self-limited and genetic-generalized epilepsy during the COVID-19 pandemic

A video case vignette: Hypermotor activity, ictal aggression, and bolting in an adolescent with an anteromedial temporal lesion

Hypnagogic Frontal EEG Bursts in Children: Epileptic or Not?

The impact of anti-seizure medications on psychiatric disorders among children with epilepsy: Both a challenge and an opportunity?

Clinical Presentation and Diagnosis of Tuberous Sclerosis Complex in Infancy

The Initial Experience of Eslicarbazepine in Children at Three Canadian Tertiary Pediatric Care Centers

Children With Trisomy 21 and Lennox-Gastaut Syndrome With Predominant Myoclonic Seizures

Original Research: Clinical Significance of a Unique Pediatric EEG Configuration: Bi-Frontal Spikes With Simultaneous Bi-Occipital Positivity

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

Lack of response to quinidine in KCNT1‐related neonatal epilepsy

Outcome of Absence Epilepsy With Onset at 8-11 Years of Age: Watershed Ages When Syndromes Overlap

Pediatric Occipital Spikes at a Single Center Over 26 Years and the Significance of Tangential Dipole

Infantile Spasms and Trisomy 21: Unfavorable Outcomes with First-line Vigabatrin Therapy

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

Co-existence of Rolandic and 3 Hz Spike-Wave Discharges on EEG in Children with Epilepsy

Predictive Value of Midline Spikes on Pediatric EEG for Seizure and Developmental Outcome

Two Patients With KCNT1-Related Epilepsy Responding to Phenobarbital and Potassium Bromide

Clinical Significance of Incidental Rolandic Spikes in Children With Absence Epilepsy

Intelligence Quotient is Not Affected by Epilepsy Surgery in Childhood

Dipolar EEG Spikes Are More Benign

At What Point Should We Discontinue Treatment in Super-Refractory Status Epilepticus?

Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5

Lack of response to quinidine in KCNT 1 ‐related neonatal epilepsy

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