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183 results

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Page 1
Association of intronic variants of the BTBD9 gene with Tourette syndrome.
Rivière JB, Xiong L, Levchenko A, St-Onge J, Gaspar C, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Rouleau GA; Montreal Tourette Study Group. Rivière JB, et al. Among authors: chouinard s. Arch Neurol. 2009 Oct;66(10):1267-72. doi: 10.1001/archneurol.2009.213. Arch Neurol. 2009. PMID: 19822783
Genome-wide TDT analysis in French-Canadian families with Tourette syndrome.
Rivière JB, St-Onge J, Gaspar C, Diab S, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Dubé MP, Rouleau GA; Montreal Tourette Study Group. Rivière JB, et al. Among authors: chouinard s. Can J Neurol Sci. 2010 Jan;37(1):110-2. doi: 10.1017/s0317167100009744. Can J Neurol Sci. 2010. PMID: 20169783 No abstract available.
LINGO1 variants in the French-Canadian population.
Bourassa CV, Rivière JB, Dion PA, Bernard G, Diab S, Panisset M, Chouinard S, Dupré N, Fournier H, Raelson J, Belouchi M, Rouleau GA. Bourassa CV, et al. Among authors: chouinard s. PLoS One. 2011 Jan 11;6(1):e16254. doi: 10.1371/journal.pone.0016254. PLoS One. 2011. PMID: 21264305 Free PMC article.
Association between 7q31 markers and Tourette syndrome.
Díaz-Anzaldúa A, Joober R, Rivière JB, Dion Y, Lespérance P, Chouinard S, Richer F, Rouleau GA; Montreal Tourette Syndrome Study Group. Díaz-Anzaldúa A, et al. Among authors: chouinard s. Am J Med Genet A. 2004 May 15;127A(1):17-20. doi: 10.1002/ajmg.a.20631. Am J Med Genet A. 2004. PMID: 15103711
Restless legs in Tourette syndrome.
Lespérance P, Djerroud N, Diaz Anzaldua A, Rouleau GA, Chouinard S, Richer F; Montréal Tourette Study Group. Lespérance P, et al. Among authors: chouinard s. Mov Disord. 2004 Sep;19(9):1084-7. doi: 10.1002/mds.20100. Mov Disord. 2004. PMID: 15372602
Glucocerebrosidase mutations in a French-Canadian Parkinson's disease cohort.
Noreau A, Rivière JB, Diab S, Dion PA, Panisset M, Soland V, Jodoin N, Langlois M, Chouinard S, Dupré N, Rouleau GA. Noreau A, et al. Among authors: chouinard s. Can J Neurol Sci. 2011 Sep;38(5):772-3. doi: 10.1017/s0317167100012300. Can J Neurol Sci. 2011. PMID: 21856586 No abstract available.
Mutations in DCC cause congenital mirror movements.
Srour M, Rivière JB, Pham JM, Dubé MP, Girard S, Morin S, Dion PA, Asselin G, Rochefort D, Hince P, Diab S, Sharafaddinzadeh N, Chouinard S, Théoret H, Charron F, Rouleau GA. Srour M, et al. Among authors: chouinard s. Science. 2010 Apr 30;328(5978):592. doi: 10.1126/science.1186463. Science. 2010. PMID: 20431009
183 results