A. Camuzat

<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Stéphanie Millecamps, François Salachas, C. Cazeneuve et al. · Journal of Medical Genetics · 2010 · 292 citations · Full text

Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism

Cécile Dumanchin, A. Camuzat, Dominique Campion et al. · Human Molecular Genetics · 1998 · 246 citations · Full text

Are interrupted <i>SCA2</i> CAG repeat expansions responsible for parkinsonism?

Perrine Charles, A. Camuzat, N. Benammar et al. · Neurology · 2007 · 164 citations

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

F. Clot, David Grabli, C. Cazeneuve et al. · Brain · 2009 · 144 citations

Exhaustive Analysis, Mendelian Disorder, Genetic Disorder +14

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

Hiroto Fujigasaki, Ishwar C. Verma, A. Camuzat et al. · Annals of Neurology · 2001 · 103 citations