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Expert Review of Neurotherapeutics|May 30, 2024
Identification and treatment of surgically-remediable causes of infantile epileptic spasms syndromeEmma Macdonald-Laurs, Winston Dzau, Aaron E L Warren, et al.
Scientific Reports|May 16, 2018
Generation and characterisation of a parkin-Pacrg knockout mouse line and a Pacrg knockout mouse lineSarah E M Stephenson, Timothy D Aumann, Juliet M Taylor, et al.
Epilepsia Open|December 3, 2022
Basal ganglia dysplasia and mTORopathy: A potential cause of postoperative seizures in focal cortical dysplasiaWei Shern Lee, Emma Macdonald-Laurs, Sarah E M Stephenson, et al.
Epilepsy Research|March 4, 2021
Resection of tuber centers only for seizure control in tuberous sclerosis complexSarah E M Stephenson, Wirginia J Maixner, Sarah M Barton, et al.
Annals of Clinical and Translational Neurology|January 12, 2021
Gradient of brain mosaic RHEB variants causes a continuum of cortical dysplasiaWei Shern Lee, Sara Baldassari, Mathilde Chipaux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 7, 2014
HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxiaMartin B Delatycki, Geneieve Tai, Louise Corben, et al.
Molecular Brain|April 2, 2020
Distribution of Parkinson's disease associated RAB39B in mouse brain tissueYujing Gao, Gabrielle R Wilson, Sarah E M Stephenson, et al.
Neurology|August 28, 2020
Genetic characterization identifies bottom-of-sulcus dysplasia as an mTORopathyWei Shern Lee, Sarah E M Stephenson, Kate Pope, et al.
Brain : a Journal of Neurology|November 8, 2023
The clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasiaEmma Macdonald-Laurs, Aaron E L Warren, Peter Francis, et al.
Annals of Clinical and Translational Neurology|July 30, 2019
Second-hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIAWei Shern Lee, Sarah E M Stephenson, Katherine B Howell, et al.
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