Désiré Magloire Bourneville and french anticlericalism during the Third RepublicBRAIS, B.Clio medica. 1993, Vol 23, pp 107-139, issn 0045-7183Article

Jean Martin Charcot and aphasia : treading the line between experimental physiology and pathological anatomyBRAIS, B.Brain and language (Print). 1993, Vol 45, Num 4, pp 511-530, issn 0093-934XArticle

Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to sporadic inclusion body myositisMEZEI, M. M; MANKODI, A; BRAIS, B et al.Neurology. 1999, Vol 52, Num 3, pp 669-670, issn 0028-3878Article

The gene responsible for Clouston hidrotic ectodermal dysplasia maps for the pericentromeric region of chromosome 13qKIBAR, Z; DER KALOUSTIAN, V. M; BRAIS, B et al.Human molecular genetics (Print). 1996, Vol 5, Num 4, pp 543-547, issn 0964-6906Article

Founder Mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian ClusterTETREAULT, M; SROUR, M; ALLYSON, J et al.Canadian journal of neurological sciences. 2011, Vol 38, Num 5, pp 747-752, issn 0317-1671, 6 p.Article

A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to IIpI3-pI2JARRY, J; RIOUX, M. F; BOLDUC, V et al.Brain. 2007, Vol 130, pp 368-380, issn 0006-8950, 13 p., 2Article

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 geneBLUMEN, S. C; KORCZYN, A. D; TOME, F. M. S et al.Neurology. 2000, Vol 55, Num 9, pp 1267-1270, issn 0028-3878Article

Diversity of ARSACS Mutations in French-CanadiansTHIFFAULT, I; DICAIRE, M. J; MCPHERSON, P. S et al.Canadian journal of neurological sciences. 2013, Vol 40, Num 1, pp 61-66, issn 0317-1671, 6 p.Article

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34THIFLAULT, I; RIOUX, M. F; BOUCHARD, J. P et al.Brain. 2006, Vol 129, pp 2332-2340, issn 0006-8950, 9 p., 9Article

A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21TETREAULT, M; DUQUETTE, A; VANASSE, M et al.Brain. 2006, Vol 129, pp 2077-2084, issn 0006-8950, 8 p., 8Article

Population history and its impact on medical genetics in QuebecLABERGE, A.-M; MICHAUD, J; RICHTER, A et al.Clinical genetics. 2005, Vol 68, Num 4, pp 287-301, issn 0009-9163, 15 p.Article

Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotesBLUMEN, S. C; BOUCHARD, J.-P; BRAIS, B et al.Neurology. 2009, Vol 73, Num 8, pp 596-601, issn 0028-3878, 6 p.Article

A novel founder SCN4A mutation causes painful cold-induced myotonia in French-CanadiansROSSIGNOL, E; MATHIEU, J; THIFFAULT, I et al.Neurology. 2007, Vol 69, Num 20, pp 1937-1941, issn 0028-3878, 5 p.Article

CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulationGASPAR, C; JANNATIPOUR, M; DION, P et al.Human molecular genetics (Print). 2000, Vol 9, Num 13, pp 1957-1966, issn 0964-6906Article

Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the diseaseBLUMEN, S. C; BRAIS, B; TOME, F. M. S et al.Annals of neurology. 1999, Vol 46, Num 1, pp 115-118, issn 0364-5134Article

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyBRAIS, B; BOUCHARD, J.-P; BLUMEN, S et al.Nature genetics. 1998, Vol 18, Num 2, pp 164-167, issn 1061-4036Article