Emilie Riou
Sherbrooke, QC, Canada
Last Updated: 09/26/2026
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Found 8 publications
Response to vagus nerve stimulation in people with ring chromosome 20.
Journal: Seizure
Published: June 18, 2025
Neurophysiological assessment of cortical activity in DEPDC5- and NPRL3-related epileptic mTORopathies.
Journal: Orphanet journal of rare diseases
Published: August 01, 2022
Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series.
Journal: Neurogenetics
Published: July 22, 2021
Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study.
Journal: Journal of child neurology
Published: July 29, 2020
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Journal: American journal of human genetics
Published: June 27, 2017
Spastic paraparesis and marked improvement of leukoencephalopathy in Aicardi-Goutières syndrome.
Journal: Neuropediatrics
Published: October 25, 2014
CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.
Journal: European journal of human genetics : EJHG
Published: July 03, 2014
Effect of lovastatin on behavior in children and adults with fragile X syndrome: an open-label study.
Journal: American journal of medical genetics. Part A
Published: March 03, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026