Jean-Pierre Bouchard

418 529-9141 # 6250

Médical doctor interested in hereditary ataxias, muscular dystrophies and neurological diseases.

Full Professor,Physician and CIRRIS Researcher Department of Medicine (Neurology) Faculty of Medicine Université Laval

Articles in scientific journals (peer-reviewed)

Bayat, V., Thiffault, I., Jaiswal, M., Tétreault, M., Donti, T., Sasarman, F., . . . Bouchard, J.-P. (2012). Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans. PLoS Biology, 10, e1001288. doi: 10.1371/journal.pbio.1001288

Belzil, V. V., André-Guimont, C., Atallah, M.-R., Daoud, H., Dupré, N., Bouchard, J.-P., . . . Rouleau, G. A. (2012). Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis. Neurobiology of Aging, 33(8), 1847-1849. doi: 10.1016/j.neurobiolaging.2012.01.011

Daoud, H., Suhail, H., Szuto, A., Camu, W., Salachas, F., Meininger, V., Bouchard, J.-P., Dupré, N., Dion, P. A. & Rouleau, G. A. (2012). UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis. Neurobiology of Aging, 33(9), 2230.e1–2230.e5.

Puymirat, J., Bouchard, J.-P. & Mathieu, J. (2012). Efficacy and Tolerability of a 20-mg Dose of Methylphenidate for the Treatment of Daytime Sleepiness in Adult Patients With Myotonic Dystrophy Type 1: A 2-Center, Randomized, Double-Blind, Placebo-Controlled, 3-Week Crossover Trial. Clinical Therapeutics, 34(5), 1103–11.

Belzil, V. V., Daoud, H., Desjarlais, A., Bouchard, J.-P., Dupré, N., Camu, W., Dion, P. A., Rouleau, G. A. (2010). Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis. Neurobiology of Aging, 32(3), 555.e13–555.e14.

Books, book chapters and contributions to collective works

Dionne, A., Bouchard, J.-P. (2011). Oculopharyngeal Muscular Dystrophy. In N. Tawil & S. Venance (Eds.) Neuromuscular Disorders. (pp. 87-90). ?:Wiley-Blackwell

CIUSSS-CN Université Laval Alliance santé Québec