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Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2019
Examining the Reserve Hypothesis in Parkinson's Disease: A Longitudinal StudyPei-Chen Lee, Fanny Artaud, Florence Cormier-Dequaire, et al.Neurology|June 22, 2018
Longitudinal analysis of impulse control disorders in Parkinson diseaseJean-Christophe Corvol, Fanny Artaud, Florence Cormier-Dequaire, et al.Journal of the National Cancer Institute|December 20, 2015
PARKIN Inactivation Links Parkinson's Disease to MelanomaHui-Han Hu, Caroline Kannengiesser, Suzanne Lesage, et al.American Journal of Human Genetics|February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humansChristel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2024
Care of Late-Stage Parkinsonism: Resource Utilization of the Disease in Five European CountriesChristopher Kruse, Anna Lipinski, Malte Verheyen, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2025
Spastic Ataxia Composite (SPAXCOM): A Scale to Evaluate the Progression of Subjects with Spasticity and AtaxiaCécile Di Folco, Charlotte Dubec-Fleury, Andreas Traschütz, et al.Brain : a Journal of Neurology|October 16, 2012
Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathyStephan Klebe, Christel Depienne, Sylvie Gerber, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 14, 2018
Comprehensive analysis of the mutation spectrum in 301 German ALS familiesKathrin Müller, David Brenner, Patrick Weydt, et al.Neurology|May 9, 2014
Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 casesAurélie Méneret, Christel Depienne, Florence Riant, et al.Nature Communications|September 3, 2024
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansionsLars Mohren, Friedrich Erdlenbruch, Elsa Leitão, et al.Pageof 10