| 14. Pre-symptomatic detection of cytoplasmic TDP-43 accumulation using tissue-engineered skin model derived from C9ORF72-FALS patients B Paré, L Touzel-Deschênes, R Lamontagne, MS Lamarre, FD Scott, ... Canadian Journal of Neurological Sciences 42 (S2), S6-S6, 2015 | | 2015 |
| 50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral … WJ Broom, M Greenway, G Sadri-Vakili, C Russ, KE Auwarter, KE Glajch, ... Amyotrophic Lateral Sclerosis 9 (4), 229-237, 2008 | 39 | 2008 |
| A Beilinson-Bernstein Theorem for Analytic Quantum Groups. I N Dupré p-Adic Numbers, Ultrametric Analysis and Applications 13 (1), 44-82, 2021 | 2 | 2021 |
| A Beilinson-Bernstein Theorem for Analytic Quantum Groups. II N Dupré p-Adic Numbers, Ultrametric Analysis and Applications 13 (2), 83-116, 2021 | | 2021 |
| A Broad Phenotype Related to a New POLG1 Mutation (P01. 121) N Chrestian, N Dupre Neurology 80 (7_supplement), P01. 121-P01. 121, 2013 | | 2013 |
| A case of familial Creutzfeldt-Jakob disease presenting with dry cough S Larue, S Verreault, P Gould, MB Coulthart, C Bergeron, N Dupré Canadian journal of neurological sciences 33 (2), 243-245, 2006 | 6 | 2006 |
| A coding VPS13C haplotype is associated with reduced risk for Parkinson disease U Rudakou, J Ruskey, L Krohn, S Laurent, D Spiegelman, L Greenbaum, ... MOVEMENT DISORDERS 34, S191-S192, 2019 | | 2019 |
| A family with anAutosomal dominant phenotype consistent with primary lateral sclerosis N Dupre, P Valdmanis, JP Bouchard, G Rouleau NEUROLOGY 68 (12), A246-A247, 2007 | | 2007 |
| A founder French-Canadian GBA mutation, p. W378G, as a cause for synucleinopathies and Gaucher disease Z Gan-Or, J Ruskey, S Zhou, L Ronciere, A Alam, D Spiegelman, ... MOVEMENT DISORDERS 33, S633-S633, 2018 | | 2018 |
| A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada PN Valdmanis, D Brunet, J St-Onge, L Weston, GA Rouleau, N Dupre Neurology 67 (12), 2239-2242, 2006 | 11 | 2006 |
| A founder mutation in French-Canadian families with X-linked hereditary neuropathy N Dupré, L Cossette, CK Hand, JP Bouchard, GA Rouleau, J Puymirat Canadian journal of neurological sciences 28 (1), 51-55, 2001 | 6 | 2001 |
| A French-Canadian family with typical essential tremor does not map to any of the known ETM loci DJ Verlaan, J St-Onge, GA Rouleau, N Dupre ANNALS OF NEUROLOGY 58, S24-S24, 2005 | | 2005 |
| A locus for primary lateral sclerosis on chromosome 4ptel-4p16. 1 PN Valdmanis, N Dupré, GA Rouleau Archives of neurology 65 (3), 383-386, 2008 | 18 | 2008 |
| A mew motor neuron disease maps to chromosome 4ptel-4p16. 1 N Dupre, P Valdmanis, G Rouleau NEUROLOGY 70 (11), A144-A144, 2008 | | 2008 |
| A mutation in the RNF170 gene causes autosomal dominant sensory ataxia PN Valdmanis, N Dupre, M Lachance, SJ Stochmanski, VV Belzil, ... Brain 134 (2), 602-607, 2011 | 40 | 2011 |
| A Mutation in the RNF170 Gene Causes Autosomal Dominant Sensory Ataxia (P05.014) N Dupre, P Valdmanis, S Stochmanski, V Belzil, P Dion, I Thiffault, B Brais, ... Neurology 78 (1_supplement), P05. 014-P05. 014, 2012 | | 2012 |
| A national spinal muscular atrophy registry for real-world evidence VL Hodgkinson, M Oskoui, J Lounsberry, S M’Dahoma, E Butler, ... Canadian Journal of Neurological Sciences 47 (6), 810-815, 2020 | 12 | 2020 |
| A novel duplication confirms the involvement of 5q23. 2 in autosomal dominant leukodystrophy IA Meijer, AA Simoes-Lopes, S Laurent, T Katz, J St-Onge, DJ Verlaan, ... Archives of neurology 65 (11), 1496-1501, 2008 | 51 | 2008 |
| A novel founder SCN4A mutation causes painful cold-induced myotonia in French-Canadians E Rossignol, J Mathieu, I Thiffault, M Tetreault, MJ Dicaire, N Chrestian, ... Neurology 69 (20), 1937-1941, 2007 | 25 | 2007 |
| A novel mutation in a large French-Canadian family with LGMD1B N Chrestian, PN Valdmanis, N Echahidi, D Brunet, JP Bouchard, P Gould, ... Canadian journal of neurological sciences 35 (3), 331-334, 2008 | 16 | 2008 |
Guy RouleauMontreal Neurological Institute-Hospital, McGill UniversityVerified email at mcgill.ca