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The Journal of Clinical Investigation|September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movementsAurélie Méneret, Elizabeth A Franz, Oriane Trouillard, 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.Human Molecular Genetics|August 14, 2003
Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouseJean-Michel Itier, Pablo Ibanez, Maria Angeles Mena, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 22, 2015
Delayed-onset Friedreich's ataxia revisitedClaire Lecocq, Perrine Charles, Jean-Philippe Azulay, et al.Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, 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.The Lancet. Neurology|June 21, 2017
Prediction of cognition in Parkinson's disease with a clinical-genetic score: a longitudinal analysis of nine cohortsGanqiang Liu, Joseph J Locascio, Jean-Christophe Corvol, et al.Brain : a Journal of Neurology|November 17, 2021
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxiaMarie Coutelier, Maxime Jacoupy, Alexandre Janer, et al.Human Mutation|May 28, 2011
REEP1 mutations in SPG31: frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunctionCyril Goizet, Christel Depienne, Giovanni Benard, et al.Brain : a Journal of Neurology|February 5, 2008
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic studyIsabelle Le Ber, Agnès Camuzat, Didier Hannequin, et al.Pageof 50