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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
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2011 9
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2016 2
2017 1
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Page 1
Molecular aspects of hereditary spastic paraplegia.
Noreau A, Dion PA, Rouleau GA. Noreau A, et al. Exp Cell Res. 2014 Jul 1;325(1):18-26. doi: 10.1016/j.yexcr.2014.02.021. Epub 2014 Mar 11. Exp Cell Res. 2014. PMID: 24631291 Review.
Therapies for ataxias.
Martineau L, Noreau A, Dupré N. Martineau L, et al. Among authors: noreau a. Curr Treat Options Neurol. 2014 Jul;16(7):300. doi: 10.1007/s11940-014-0300-y. Curr Treat Options Neurol. 2014. PMID: 24832479
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals.
Girard SL, Bourassa CV, Lemieux Perreault LP, Legault MA, Barhdadi A, Ambalavanan A, Brendgen M, Vitaro F, Noreau A, Dionne G, Tremblay RE, Dion PA, Boivin M, Dubé MP, Rouleau GA. Girard SL, et al. Among authors: noreau a. PLoS One. 2016 Oct 10;11(10):e0164212. doi: 10.1371/journal.pone.0164212. eCollection 2016. PLoS One. 2016. PMID: 27723766 Free PMC article.
Exome sequencing identifies FUS mutations as a cause of essential tremor.
Merner ND, Girard SL, Catoire H, Bourassa CV, Belzil VV, Rivière JB, Hince P, Levert A, Dionne-Laporte A, Spiegelman D, Noreau A, Diab S, Szuto A, Fournier H, Raelson J, Belouchi M, Panisset M, Cossette P, Dupré N, Bernard G, Chouinard S, Dion PA, Rouleau GA. Merner ND, et al. Among authors: noreau a. Am J Hum Genet. 2012 Aug 10;91(2):313-9. doi: 10.1016/j.ajhg.2012.07.002. Epub 2012 Aug 2. Am J Hum Genet. 2012. PMID: 22863194 Free PMC article.
Exome sequencing reveals SPG11 mutations causing juvenile ALS.
Daoud H, Zhou S, Noreau A, Sabbagh M, Belzil V, Dionne-Laporte A, Tranchant C, Dion P, Rouleau GA. Daoud H, et al. Among authors: noreau a. Neurobiol Aging. 2012 Apr;33(4):839.e5-9. doi: 10.1016/j.neurobiolaging.2011.11.012. Epub 2011 Dec 10. Neurobiol Aging. 2012. PMID: 22154821
35 results