Brandon F. Meaney
Hamilton, ON, Canada
Last Updated: 09/26/2026
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Found 12 publications
PRRT 2-Related Epilepsy: From Self-Limited Infantile Epilepsy to Atypical Epilepsy Phenotypes.
Journal: Neurology. Genetics
Published: November 04, 2024
Significant vomiting and weight loss in a pediatric epilepsy patient secondary to vagus nerve stimulation: A case report and review of the literature.
Journal: Epilepsy & behavior reports
Published: July 28, 2023
The epilepsy phenotype of ST3GAL3-related developmental and epileptic encephalopathy.
Journal: Epilepsia open
Published: March 17, 2023
Functional Effects of Epilepsy Associated KCNT1 Mutations Suggest Pathogenesis via Aberrant Inhibitory Neuronal Activity.
Journal: International journal of molecular sciences
Published: November 04, 2022
The spectrum of epilepsy in children with 15q13.3 microdeletion syndrome.
Journal: Seizure
Published: July 15, 2021
A recurrent de novo HSPD1 variant is associated with hypomyelinating leukodystrophy.
Journal: Cold Spring Harbor molecular case studies
Published: December 20, 2019
Feasibility and Reliability of Muscle Strength Testing in Critically Ill Children.
Journal: Journal of pediatric intensive care
Published: December 08, 2014
Encephalitis with refractory seizures, status epilepticus, and antibodies to the GABAA receptor: a case series, characterisation of the antigen, and analysis of the effects of antibodies.
Journal: The Lancet. Neurology
Published: January 28, 2014
Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C.
Journal: American journal of medical genetics. Part A
Published: January 09, 2013
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Last Updated: 09/26/2026