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Journal of Child Neurology|May 7, 2003
Pediatric neurology services in Canada: demand versus supplyGabriel M Ronen, Brandon F Meaney
Epilepsy & Behavior : E&B|October 31, 2013
SUDEP: what do parents want to know?Rajesh Ramachandrannair, Susan M Jack, Brandon F Meaney, et al.
Cold Spring Harbor Molecular Case Studies|June 14, 2020
A recurrent de novo HSPD1 variant is associated with hypomyelinating leukodystrophyCagla Cömert, Lauren Brick, Debbie Ang, et al.
American Journal of Human Genetics|April 23, 2003
Ovarian failure related to eukaryotic initiation factor 2B mutationsAnne Fogli, Diana Rodriguez, Eléonore Eymard-Pierre, et al.
Seizure|October 3, 2021
The spectrum of epilepsy in children with 15q13.3 microdeletion syndromeRobyn Whitney, Arjun Nair, Elizabeth McCready, et al.
Molecular Metabolism|August 15, 2024
HSP60 chaperone deficiency disrupts the mitochondrial matrix proteome and dysregulates cholesterol synthesisCagla Cömert, Kasper Kjær-Sørensen, Jakob Hansen, et al.
International Journal of Molecular Sciences|December 11, 2022
Functional Effects of Epilepsy Associated KCNT1 Mutations Suggest Pathogenesis via Aberrant Inhibitory Neuronal ActivityGrigori Y Rychkov, Zeeshan Shaukat, Chiao Xin Lim, et al.
The Lancet. Neurology|January 28, 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 antibodiesMar Petit-Pedrol, Thaís Armangue, Xiaoyu Peng, et al.
Neurology. Genetics|May 22, 2025
PRRT 2-Related Epilepsy: From Self-Limited Infantile Epilepsy to Atypical Epilepsy PhenotypesMadeline Komar, Jashanpreet Sidhu, Jiju Joseph, et al.
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