Publications
Résultats 431 à 440 sur 558 Publications
| Titre | Auteurs | Année | Revue |
|---|---|---|---|
| The GBA p Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies | Ruskey, J.A., Zhou, S., Santiago, R., Franche, L.A., Alam, A., Ronciere, L., Spiegelman, D., Fon, E.A., Trempe, J.F., Kalia, L.V., Postuma, R.B., Dupre, N., Rivard, G.E., Assouline, S., Amato, D., & Gan-Or, Z. | 2018 | Clinical Genetics |
| The Canadian Dementia Imaging Protocol: Harmonizing national cohorts | Duchesne, S., Chouinard, I., Potvin, O., Fonov, V.S., Khademi, A., Bartha, R., Bellec, P., Collins, D.L., Descoteaux, M., Hoge, R., McCreary, C.R., Ramirez, J., Scott, C.J.M., Smith, E.E., Strother, S.C., Black, S.E. | 2018 | Journal of Magnetic Resonance Imaging |
| APP21 transgenic rats develop age-dependent cognitive impairment and microglia accumulation within white matter tracts | Weishaupt, N., Liu, Q., Shin, S., Singh, R., Agca, Y., Agca, C., Hachinski, V., & Whitehead, S.N. | 2018 | Journal of Neuroinflammation |
| In vivo quantification of neurofibrillary tangles with [(18)F]MK-6240 | Pascoal, T. A., Shin, M., Kang, M. S., Chamoun, M., Chartrand, D., Mathotaarachchi, S., Bennacef, I., Therriault, J., Ng, K. P., Hopewell, R., Bouhachi, R., Hsiao, H. H., Benedet, A. L., Soucy, J. P., Massarweh, G., Gauthier, S., & Rosa-Neto, P. | 2018 | Alzheimer's Research and Therapy |
| Frequency of loss of function variants in LRRK2 in Parkinson Disease | Blauwendraat, C., Reed, X., Kia, D.A., Gan-Or, Z., Lesage, S., Pihlstrom, L., Guerreiro, R., Gibbs, J.R., Sabir M., Ahmed, S., Ding, J., Alcalay, R.N., Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. Hassin-Baer, S., Pittma,n A.M., Brooks, J., Edsall, C., Hernandez, D.G., Chung, S.J., Goldwurm, S., Toft, M., Schulte, C., Bras, J., Wood, N.W., Brice, A., Morris, H.R., Scholz, S.W., Nalls, M.A., Singleton, A.B., Cookson, M.R., for the COURAGE-PD Consortium, the French Parkinson's Disease Consortium, & the International Parkinson's Disease Genomics Consortium. | 2018 | JAMA Neurology |
| Consent recommendations for research and international data sharing involving persons with dementia | Thorogood, A., Mäki-Petäjä-Leinonen, A., Brodaty, H., Dalpé, G., Gastmans, C., Gauthier, S., Gove, D., Harding, R., Knoppers, B. M., Rossor, M., & Bobrow, M. | 2018 | Alzheimer's & Dementia |
| Patient engagement in research related to dementia: a scoping review | Bethell, J., Commisso, E., Rostad, H.M., Puts, M., Babineau, J., Grinbergs-Saull, A., Wighton, M.B., Hammel, J., Doyle, E., Nadeau, S. & McGilton K.S. | In press | Dementia |
| Full sequencing and haplotype analysis of MAPT in Parkinson’s disease and rapid eye movement sleep behavior disorder | Li, J., Ruskey, J.A., Arnulf, I., Dauvilliers, Y., Hu, M.T.M., Hogl, B., Leblond, C.S., Zhou, S., Ambalavanan, A., Ross, J.P., Bourassa, C.V., Spiegelman, D., Laurent, S.B., Stefani, A., Charley Monaca, C., Cochen De Cock, V., Boivin, M., Ferini-Strambi, L., Plazzi, G., Antelmi, E., Young, P., Heidbreder, A., Labbe, C., Ferman, T.J., Dion, P.A., Fan, D., Desautels, A., Gagnon, J.F., Dupre, N., Fon, E.A., Montplaisir, J.Y., Boeve, B.F., Postuma, R.B., Rouleau, G.A., Ross, O.A., & Gan-Or, Z. | 2018 | Movement Disorders |
| Care of community-dwelling older adults with dementia and their caregivers | Warrick, N., Prorok, J. C., & Seitz, D. | 2018 | Canadian Medical Association Journal |
| LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder | Ouled, A.B.B., Ruskey, J.A., Arnulf, I., Dauvilliers, Y., Monaca, C.C., De Cock, V.C., Gagnon, J.F., Spiegelman, D., Hu, M.T.M., Hogl, B., Stefani, A., Ferini-Strambi, L., Plazzi, G., Antelmi, E., Young, P., Heidbreder, A., Mollenhauer, B., Sixel-Doring, F., Trenkwalder, C., Oertel, W., Montplaisir, J.Y., Postuma, R.B., Rouleau, G.A., & Gan-Or, Z. | 2018 | Parkinsonism and Related Disorders |
Résultats 431 à 440 sur 558 Publications