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Journal of Alzheimer'S Disease : JAD|December 16, 2010
FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosisOriane Broustal, Agnès Camuzat, Lena Guillot-Noël, et al.Brain : a Journal of Neurology|May 16, 2025
Linking polygenic risk scores to dopaminergic neuron loss using neuromelanin-sensitive imagingAymeric Lanore, Rahul Gaurav, François-Xavier Lejeune, et al.Plos One|March 20, 2012
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's diseaseJavier Simón-Sánchez, Laura L Kilarski, Michael A Nalls, et al.Brain : a Journal of Neurology|March 23, 2013
Interferon β induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in miceAlice Chort, Sandro Alves, Martina Marinello, et al.JAMA Neurology|August 21, 2013
SYNE1 mutations in autosomal recessive cerebellar ataxiaAnne Noreau, Cynthia V Bourassa, Anna Szuto, et al.Journal of Alzheimer'S Disease : JAD|August 13, 2014
A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutationClaire Boutoleau-Bretonnière, Agnès Camuzat, Isabelle Le Ber, et al.Brain : a Journal of Neurology|September 25, 2003
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studiesIsabelle Le Ber, Maria-Ceù Moreira, Sophie Rivaud-Péchoux, et al.Archives of Neurology|June 12, 2002
Association between the extended tau haplotype and frontotemporal dementiaPatrice Verpillat, Agnès Camuzat, Didier Hannequin, et al.Neurobiology of Aging|December 16, 2011
Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosisStéphanie Millecamps, Philippe Corcia, Cécile Cazeneuve, et al.Movement Disorders Clinical Practice|April 18, 2023
Detection of <i>ATXN2</i> Expansions in an Exome Dataset: An Underdiagnosed Cause of ParkinsonismFanny Casse, Thomas Courtin, Christelle Tesson, et al.Pageof 50