- Overview
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Research is primarily focused on epilepsy in the pediatric population.
- Publications
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The curious case of the gene, the lesion, or neither
Epileptic Disorders
Alexander Freibauer and Bashayer Almohaimeed and Anita Datta
DOI: 10.1002/epd2.20293
10/2024The Initial Experience of Eslicarbazepine in Children at Three Canadian Tertiary Pediatric Care Centers
Journal of Child Neurology
Yvonne Nyakeri and Qi Xu and Maryam Nouri and Denait Haile and Anita N. Datta
DOI: 10.1177/08830738241282903
10/2024Original Research: Clinical Significance of a Unique Pediatric EEG Configuration: Bi-Frontal Spikes With Simultaneous Bi-Occipital Positivity
Clinical EEG and Neuroscience
Jacqueline Crawford and Cassie McFarlane and Anita N Datta
DOI: 10.1177/15500594241246505
09/2024Case Report: Successful complete open corpus callosotomy for refractory epilepsy in Rett syndrome
Brain and Development Case Reports
Anita N. Datta and Mandeep Tamber
DOI: 10.1016/j.bdcasr.2024.100032
09/2024Developmental and epileptic encephalopathies after successful treatment of pediatric ALL: A case series and review of literature
Epileptic Disorders
Vanita Shukla and Sylvia Cheng and Juliette Hukin and Linda Huh and Anita N. Datta
DOI: 10.1002/epd2.20280
09/2024A video case vignette: Hypermotor activity, ictal aggression, and bolting in an adolescent with an anteromedial temporal lesion
Epileptic Disorders
Anita N. Datta
DOI: 10.1002/epd2.20176
04/2024Effectiveness, safety and tolerability of perampanel by age group when used to treat people with focal and generalized epilepsy in clinical practice: The PERMIT Extension study
Epilepsy & Behavior
James Wheless and Robert T. Wechsler and Patricia Penovich and Eric Segal and Michael Chez and Antonietta Coppola and Anita Datta and Wendyl D'Souza and Imad Najm and Sheri Cappucci and Ricardo Sainz-Fuertes and Vicente Villanueva
DOI: 10.1016/j.yebeh.2023.109369
10/2023Outcome of Absence Epilepsy With Onset at 8-11 Years of Age: Watershed Ages When Syndromes Overlap
Journal of Child Neurology
Anita N. Datta and Jacqueline Crawford and Laura Wallbank and Peter K. H. Wong
DOI: 10.1177/08830738231188397
08/2023Three consecutive epilepsy syndromes in one child
Epileptic Disorders
Min Jung Kim and Linda Huh and Anita N. Datta
DOI: 10.1002/epd2.20051
02/2023School 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
Anita N. Datta and Peter K.H. Wong
DOI: 10.1177/03000605221081032
04/2022Children With Trisomy 21 and Lennox-Gastaut Syndrome With Predominant Myoclonic Seizures
Journal of Child Neurology
Matthew Macdonald and Jacqueline Crawford and Anita N. Datta
DOI: 10.1177/08830738211026072
10/2021Pediatric Occipital Spikes at a Single Center Over 26 Years and the Significance of Tangential Dipole
Journal of Child Neurology
Anita N. Datta and Laura Wallbank and Johann Micallef and Peter K. H. Wong
DOI: 10.1177/0883073820984042
06/2021At What Point Should We Discontinue Treatment in Super-Refractory Status Epilepticus?
Journal of Pediatric Epilepsy
Anita N. Datta
DOI: 10.1055/s-0040-1714389
09/2020Childhood Small Vessel Primary Angiitis of the Central Nervous System: A Treatable Cause of Super-refractory Status Epilepticus
Journal of Child Neurology
Michelle Chiu and Anita Datta
DOI: 10.1177/0883073819872579
01/2020Clinical Significance of Incidental Rolandic Spikes in Children With Absence Epilepsy
Journal of Child Neurology
Anita N. Datta and Laura Wallbank and Jeremy C. H. Mak and Peter K. H. Wong
DOI: 10.1177/0883073819848639
10/2019Two Patients With KCNT1-Related Epilepsy Responding to Phenobarbital and Potassium Bromide
Journal of Child Neurology
Anita N. Datta and Aspasia Michoulas and Ilaria Guella and Michelle Demos
DOI: 10.1177/0883073819854853
10/2019Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy
Journal of Human Genetics
DOI: 10.1016/j.ajhg.2017.05.016
06/2017An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2
Pediatric Neurology
DOI: 10.1016/j.pediatrneurol.2017.06.003
06/2017Clinical Experience With Perampanel For Refractory Pediatric Epilepsy In One Canadian Center
Journal of Child Neurology
DOI: 10.1177/0883073817709195
05/2017Predictors of IQ After Pediatric Epilepsy Surgery
Scientific Times Journal of Paediatrics
02/2017Case Report: QARS Deficiency and Favorable Outcomes Following Treatment of Seizures With Ketogenic Diet
Journal of Child Neurology
DOI: 10.1177/0883073816685508
01/2017Manifestations of Tuberous Sclerosis Complex: The Experience of a Provincial Clinic
Canadian Journal Neurological Sciences
DOI: 10.1017/cjn.2016.311
2017Care of Children with Epilepsy at BC Children's Hospital
The Official Journal of the Hong Kong Society of Child Neurology and Developmental Paediatrics
2016DRESS and PRES in a Patient With Epilepsy: Unexpected Consequences of Adding Lamotrigine
Scientific Times Journal of Paediatrics
2016 - Research
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Clinical Experience with Perampanel in the Pediatric Population in two Canadian Centers
The purpose of this study is to describe the efficacy, tolerability and side effects of Perampanel in pediatric patients with refractory epilepsy. To do so, a retrospective detailed chart review of eligible patients at BCCH will be completed.Impact of Pediatric Epilepsy Surgery on Health-Related Quality Of Life
The objective of this study is to evaluate the effectiveness of two treatments, epilepsy surgery relative to medical therapy, on improving health related quality of life (HRQL) longitudinally. The surgical group will be compared to a medical treatment group which has undergone work-up for surgery but deemed unsuitable for surgery. These two groups have been shown to have similar baseline characteristics. Outcome will be addressed using a novel comprehensive model that acknowledges a number of variables such as clinical status (seizure control), patient factors (mood and self-concept) and family factors (caregivers’ mood, family adaptation, resources and demands) can affect changes in HRQL.A three-arm, randomized, double-blind, placebo-controlled study of the efficacy and safety of two trough-ranges of everolimus as adjunctive therapy in patients with tuberous sclerosis complex (TSC) who have refractory partial-onset seizures
The main purpose of this study is to find out if the drug everolimus (Afinitor®) is safe and has helpful effects in patients with tuberous sclerosis complex (TSC) who have refractory partial-onset seizures. These are seizures that involve some type of body movement and are not adequately responding to ongoing treatment with epilepsy drugs. Many patients with TSC develop seizures. We are not sure if the seizures are caused by growth of certain cells in the brain or by changes in the way cells in the brain work together. Studies in animals that have changes in their brain similar to those seen with TSC, have demonstrated that seizures can be reduced by use of the everolimus.Honours & AwardsTopScholar Epilepsy Fellow, Seattle, WA; supported by an educational grant from Ortho-McNeil Neurologics, Inc. (December 2008)
Annual Meeting Resident Scholarship, American Academy of Neurology (2006)
Research Group MembersVicky Cao, Summer Student
Katarina Krivokapic, Summer Student
Vesna Popovska, Research Director, Pediatric Neurology & Neurosurgery
Congratulations CIHR Spring 2024 Project Grant recipients
Congratulations to the BC Children’s Hospital Research Institute (BCCHR) and Women’s Health Research Institute (WHRI) investigators and their teams who were awarded $5 million in funding through the Canadian Institutes of Health Research (CIHR) Spring 2024 Project Grant competition.