Paraparésies spastiques héréditai res: webneurol approche clinique et génétique = Hereditary spastic paraplegia: clinical and genetic approachCHRESTIAN, Nicolas; DUPRE, Nicolas.Neurologie.com. 2010, Vol 2, Num 8, pp 206-210, issn 2100-9511, 5 p.Article

Control of LiFePO₄ air-aging through the use of electrolyte additiveCUISINIER, Marine; DUPRE, Nicolas; GUYOMARD, Dominique et al.Electrochemistry communications. 2014, Vol 38, pp 138-141, issn 1388-2481, 4 p.Article

Adrenomyeloneuropathy : Report of a new mutation in a French Canadian femaleDIONNE, Annie; BRUNET, Denis; MCCAMPBELL, Alexander et al.Canadian journal of neurological sciences. 2005, Vol 32, Num 2, pp 261-263, issn 0317-1671, 3 p.Article

Intra-Arterial Milrinone for Reversible Cerebral Vasoconstriction SyndromeBOUCHARD, Manon; VERREAULT, Steve; GARIEPY, Jean-Luc et al.Headache. 2009, Vol 49, Num 1, pp 142-145, issn 0017-8748, 4 p.Article

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian populationDUPRE, Nicolas; BOUCHARD, Jean-Pierre; BRAIS, Bernard et al.Canadian journal of neurological sciences. 2006, Vol 33, Num 2, pp 149-157, issn 0317-1671, 9 p.Article

⁷Li and ⁵¹V MAS NMR study of the electrochemical behavior of Li_1+xV₃O₈DUPRE, Nicolas; GAUBICHER, Joel; GUYOMARD, Dominique et al.Chemistry of materials. 2004, Vol 16, Num 14, pp 2725-2733, issn 0897-4756, 9 p.Article

PROPOFOL-RELATED INFUSION SYNDROME HERALDING A MITOCHONDRIAL DISEASE: CASE REPORTSAVARD, Martin; DUPRE, Nicolas; TURGEON, Alexis F et al.Neurology. 2013, Vol 81, Num 8, pp 770-771, issn 0028-3878, 2 p.Article

Detection of surface layers using ⁷Li MAS NMRDUPRE, Nicolas; MARTIN, Jean-Frédéric; GUYOMARD, Dominique et al.Journal of material chemistry. 2008, Vol 18, Num 36, pp 4266-4273, issn 0959-9428, 8 p.Article

SPG4 founder effect in french canadians with hereditary spastic paraplegiaMEIJER, Inge. A; DUPRE, Nicolas; BRAIS, Bernard et al.Canadian journal of neurological sciences. 2007, Vol 34, Num 2, pp 211-214, issn 0317-1671, 4 p.Article

A founder mutation in french-canadian families with X-linked hereditary neuropathyDUPRE, Nicolas; COSSETTE, Louise; HAND, Collette K et al.Canadian journal of neurological sciences. 2001, Vol 28, Num 1, pp 51-55, issn 0317-1671Article

Moisture driven aging mechanism of LiFeP0₄ subjected to air exposureCUISINIER, Marine; MARTIN, Jean-Frédéric; DUPRE, Nicolas et al.Electrochemistry communications. 2010, Vol 12, Num 2, pp 238-241, issn 1388-2481, 4 p.Article

A novel TYMP mutation in a French Canadian patient with mitochondrial neurogastrointestinal encephalomyopathyLAFORCE, Robert; VALDMANIS, Paul N; DUPRE, Nicolas et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2009, Vol 111, Num 8, pp 691-694, issn 0303-8467, 4 p.Article

Characterization of interphases appearing on LiNi_0.5Mn_0.5O₂ using ⁷Li MAS NMRDUPRE, Nicolas; MARTIN, Jean-Frédéric; GUYOMARD, Dominique et al.Journal of power sources (Print). 2009, Vol 189, Num 1, pp 557-560, issn 0378-7753, 4 p.Conference Paper

Unique control of bulk reactivity by surface phenomena in a positive electrode of lithium batteryDUPRE, Nicolas; MARTIN, Jean-Frédéric; OLIVERI, Julie et al.Electrochemistry communications. 2008, Vol 10, Num 12, pp 1897-1900, issn 1388-2481, 4 p.Article

Autosomal dominant primary lateral sclerosisDUPRE, Nicolas; VALDMANIS, Paul N; BOUCHARD, Jean-Pierre et al.Neurology. 2007, Vol 68, Num 14, pp 1156-1157, issn 0028-3878, 2 p.Article

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1DUPRE, Nicolas; GROS-LOUIS, Francois; CHRESTIAN, Nicolas et al.Annals of neurology. 2007, Vol 62, Num 1, pp 93-98, issn 0364-5134, 6 p.Article

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9pVALDMANIS, Paul N; DUPRE, Nicolas; BOUCHARD, Jean-Pierre et al.Archives of neurology (Chicago). 2007, Vol 64, Num 2, pp 240-245, issn 0003-9942, 6 p.Article

Combined neutron diffraction, NMR, and electrochemical investigation of the layered-to-spinel transformation in LiMnO₂ARMSTRONG, A. Robert; DUPRE, Nicolas; PATERSON, Allan J et al.Chemistry of materials. 2004, Vol 16, Num 16, pp 3106-3118, issn 0897-4756, 13 p.Article

A mutation in the RNF170 gene causes autosomal dominant sensory ataxiaVALDMANIS, Paul N; DUPRE, Nicolas; SAMUELS, Mark E et al.Brain. 2011, Vol 134, pp 602-607, issn 0006-8950, 6 p., 2Article

Relationship between surface chemistry and electrochemical behavior of LiNi_1/2Mn_1/2O₂ positive electrode in a lithium-ion batteryDUPRE, Nicolas; MARTIN, Jean-Frederic; OLIVERI, Julie et al.Journal of power sources (Print). 2011, Vol 196, Num 10, pp 4791-4800, issn 0378-7753, 10 p.Article

Aging of the LiFeP0₄ positive electrode interface in electrolyteDUPRE, Nicolas; MARTIN, Jean-Frédéric; DEGRYSE, Jeremy et al.Journal of power sources (Print). 2010, Vol 195, Num 21, pp 7415-7425, issn 0378-7753, 11 p.Article

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxiaGROS-LOUIS, Francois; DUPRE, Nicolas; DION, Patrick et al.Nature genetics. 2007, Vol 39, Num 1, pp 80-85, issn 1061-4036, 6 p.Article

Une nouvelle forme d'ataxie récessive causée par des mutations du gène SYNE-1 = Mutations in SYNE-I lead to a newly discovered form of autosomal recessive cerebellar ataxiaDUPRE, Nicolas; BOUCHARD, Jean-Pierre; GROS-LOUIS, Francois et al.MS. Médecine sciences. 2007, Vol 23, Num 3, pp 261-262, issn 0767-0974, 2 p.Article

Hereditary motor and sensory neuropathy with agenesis of the corpus callosumDUPRE, Nicolas; HOWARD, Heidi C; MATHIEU, Jean et al.Annals of neurology. 2003, Vol 54, Num 1, pp 9-18, issn 0364-5134, 10 p.Article

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformationDUPRE, Nicolas; VERLAAN, Dominique J; ROULEAU, Guy A et al.Canadian journal of neurological sciences. 2003, Vol 30, Num 2, pp 122-128, issn 0317-1671, 7 p.Article