E. Riou

发表

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

François Dubeau, Guillaume Bourque, Ange-Line Bruel, 2017, American journal of human genetics.

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms

L. Gagnon, E. Rossignol, A. Lortie, 2015, European Journal of Human Genetics.

Global developmental delay and its relationship to cognitive skills

M. Shevell, E. Riou, Shuvo Ghosh, 2009, Developmental medicine and child neurology.

Toward the definition of cerebral arteriopathies of childhood

H. Fullerton, G. deVeber, G. Sébire, 2004, Current opinion in pediatrics.

Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study

M. Tarnopolsky, B. Brais, S. Chénier, 2020, Journal of child neurology.

Cerebrospinal fluid analysis in the diagnosis and treatment of arterial ischemic stroke.

C. Amlie-Lefond, G. Sébire, E. Riou, 2008, Pediatric neurology.

Spastic Paraparesis and Marked Improvement of Leukoencephalopathy in Aicardi–Goutières Syndrome

B. Brais, S. Lévesque, G. Bernard, 2014, Neuropediatrics.

Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series

S. Lévesque, N. Braverman, G. Bernard, 2022, neurogenetics.

Acute combined central and peripheral nervous system demyelination in children.

G. Bernard, C. Poulin, T. Adamović, 2008, Pediatric neurology.

Effect of lovastatin on behavior in children and adults with fragile X syndrome: An open‐label study

E. Riou, F. Corbin, D. Pellerin, 2014, American journal of medical genetics. Part A.

Simultaneous Guillain-Barré Syndrome and Acute Disseminated Encephalomyelitis in the Pediatric Population

B. Rosenblatt, G. Bernard, C. Poulin, 2008, Journal of child neurology.