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Acta Neuropathologica|June 21, 2005
Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a familyO Martinaud, A Laquerrière, L Guyant-Maréchal, et al.Neurology|March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patientsG Stevanin, A Camuzat, S E Holmes, et al.Human Molecular Genetics|September 16, 1998
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonismC Dumanchin, A Camuzat, D Campion, et al.Neurology|November 30, 2006
Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystoniaI Le Ber, F Clot, L Vercueil, et al.European Journal of Human Genetics : EJHG|September 12, 2000
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French populationL Zurutuza, P Verpillat, G Raux, et al.Annals of Neurology|February 24, 2001
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian familyH Fujigasaki, I C Verma, A Camuzat, et al.Nature Genetics|December 1, 1996
Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosisI Perrault, J M Rozet, P Calvas, et al.American Journal of Human Genetics|August 12, 1999
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrumD Campion, C Dumanchin, D Hannequin, et al.Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.Neurology|May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseI Le Ber, A Camuzat, E Berger, et al.Pageof 2