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Neurobiology of Disease|February 26, 2021
Plasma neurofilament light chain predicts cerebellar atrophy and clinical progression in spinocerebellar ataxiaGiulia Coarelli, Frederic Darios, Emilien Petit, et al.Journal of Neurology|February 28, 2006
Neurophysiological evidence of corticospinal tract abnormality in patients with Parkin mutationsAnna De Rosa, Giampiero Volpe, Lucia Marcantonio, et al.Journal of Neurology|July 14, 2010
CHMP2B mutations are rare in French families with frontotemporal lobar degenerationMustapha Ghanim, Léna Guillot-Noel, Florence Pasquier, et al.The European Journal of Neuroscience|April 23, 2005
Akt is altered in an animal model of Huntington's disease and in patientsEmilie Colin, Etienne Régulier, Valérie Perrin, et al.European Journal of Human Genetics : EJHG|October 25, 2007
Mental deficiency in three families with SPG4 spastic paraplegiaPascale Ribaï, Christel Depienne, Estelle Fedirko, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 16, 2015
Sleep aspects on video-polysomnography in LRRK2 mutation carriersMickael Ehrminger, Smaranda Leu-Semenescu, Florence Cormier, et al.Human Mutation|October 28, 2006
Deletion of the parkin and PACRG gene promoter in early-onset parkinsonismSuzanne Lesage, Periquet Magali, Ebba Lohmann, et al.Brain : a Journal of Neurology|January 13, 2006
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North AfricaPablo Ibáñez, Suzanne Lesage, Ebba Lohmann, et al.Journal of Neurology|July 26, 2002
Association study between iron-related genes polymorphisms and Parkinson's diseaseClaire Borie, Francesca Gasparini, Patrice Verpillat, et al.Human Mutation|March 6, 2009
Partial deletion of the MAPT gene: a novel mechanism of FTDP-17Anne Rovelet-Lecrux, Magalie Lecourtois, Catherine Thomas-Anterion, et al.Pageof 50