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Parkinsonism & Related Disorders|December 21, 2005
Movement disorders and Creutzfeldt-Jakob disease: a reviewDavid Maltête, Lucie Guyant-Maréchal, Bruno Mihout, et al.American Journal of Medical Genetics. Part A|March 18, 2011
Juvenile Huntington disease in an 18-month-old boy revealed by global developmental delay and reduced cerebellar volumeGaël Nicolas, Didier Devys, Alice Goldenberg, et al.The British Journal of Psychiatry : the Journal of Mental Science|July 2, 2010
Morbid risk for schizophrenia in first-degree relatives of people with frontotemporal dementiaDelphine Schoder, Didier Hannequin, Olivier Martinaud, et al.American Journal of Medical Genetics. Part A|November 10, 2005
Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotypeLucie Guyant-Maréchal, Aad Verrips, Carole Girard, et al.Neurology|October 19, 2012
PRRT2 mutations cause hemiplegic migraineFlorence Riant, Emmanuel Roze, Cecile Barbance, et al.Diagnostics (Basel, Switzerland)|September 28, 2021
An Atypical Case of Head Tremor and Extensive White Matter in an Adult Female Caused by 3-Hydroxy-3-methylglutaryl-CoA Lyase DeficiencyNassim Boutouchent, Julie Bourilhon, Bénédicte Sudrié-Arnaud, et al.Journal of Clinical Neuromuscular Disease|May 25, 2017
Cardiac Abnormalities in Type 1 Facioscapulohumeral Muscular DystrophyFabien Labombarda, Maxime Maurice, Jean-Philippe Simon, et al.Pediatric Radiology|June 22, 2018
Morphological features in juvenile Huntington disease associated with cerebellar atrophy - magnetic resonance imaging morphometric analysisAbderrahmane Hedjoudje, Gaël Nicolas, Alice Goldenberg, et al.Brain : a Journal of Neurology|September 9, 2006
Phenotype associated with APP duplication in five familiesLucie Cabrejo, Lucie Guyant-Maréchal, Annie Laquerrière, et al.Neurobiology of Aging|July 15, 2018
Novel VCP mutations expand the mutational spectrum of frontotemporal dementiaDario Saracino, Fabienne Clot, Agnès Camuzat, et al.Pageof 3