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Page 1
Early detection of structural abnormalities and cytoplasmic accumulation of TDP-43 in tissue-engineered skins derived from ALS patients.
Paré B, Touzel-Deschênes L, Lamontagne R, Lamarre MS, Scott FD, Khuong HT, Dion PA, Bouchard JP, Gould P, Rouleau GA, Dupré N, Berthod F, Gros-Louis F. Paré B, et al. Among authors: bouchard jp. Acta Neuropathol Commun. 2015 Jan 31;3:5. doi: 10.1186/s40478-014-0181-z. Acta Neuropathol Commun. 2015. PMID: 25637145 Free PMC article.
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, Vande Velde C, Bouchard JP, Lacomblez L, Pochigaeva K, Salachas F, Pradat PF, Camu W, Meininger V, Dupre N, Rouleau GA. Kabashi E, et al. Among authors: bouchard jp. Nat Genet. 2008 May;40(5):572-4. doi: 10.1038/ng.132. Epub 2008 Mar 30. Nat Genet. 2008. PMID: 18372902
Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.
Gros-Louis F, Andersen PM, Dupre N, Urushitani M, Dion P, Souchon F, D'Amour M, Camu W, Meininger V, Bouchard JP, Rouleau GA, Julien JP. Gros-Louis F, et al. Among authors: bouchard jp. Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21777-82. doi: 10.1073/pnas.0902174106. Epub 2009 Dec 9. Proc Natl Acad Sci U S A. 2009. PMID: 20007371 Free PMC article.
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis.
Belzil VV, Daoud H, Desjarlais A, Bouchard JP, Dupré N, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: bouchard jp. Neurobiol Aging. 2011 Mar;32(3):555.e13-4. doi: 10.1016/j.neurobiolaging.2010.10.001. Epub 2010 Nov 11. Neurobiol Aging. 2011. PMID: 21074290
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.
Leblond CS, Gan-Or Z, Spiegelman D, Laurent SB, Szuto A, Hodgkinson A, Dionne-Laporte A, Provencher P, de Carvalho M, Orrù S, Brunet D, Bouchard JP, Awadalla P, Dupré N, Dion PA, Rouleau GA. Leblond CS, et al. Among authors: bouchard jp. Neurobiol Aging. 2016 Jan;37:209.e17-209.e21. doi: 10.1016/j.neurobiolaging.2015.09.013. Epub 2015 Sep 28. Neurobiol Aging. 2016. PMID: 26493020
Autosomal dominant primary lateral sclerosis.
Dupré N, Valdmanis PN, Bouchard JP, Rouleau GA. Dupré N, et al. Among authors: bouchard jp. Neurology. 2007 Apr 3;68(14):1156-7. doi: 10.1212/01.wnl.0000258678.58808.86. Neurology. 2007. PMID: 17404201 No abstract available.
Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.
Belzil VV, Daoud H, St-Onge J, Desjarlais A, Bouchard JP, Dupre N, Lacomblez L, Salachas F, Pradat PF, Meininger V, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: bouchard jp. Amyotroph Lateral Scler. 2011 Mar;12(2):113-7. doi: 10.3109/17482968.2010.536840. Epub 2011 Jan 24. Amyotroph Lateral Scler. 2011. PMID: 21261515
Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.
Belzil VV, André-Guimont C, Atallah MR, Daoud H, Dupré N, Bouchard JP, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: bouchard jp. Neurobiol Aging. 2012 Aug;33(8):1845.e7-9. doi: 10.1016/j.neurobiolaging.2012.01.011. Epub 2012 Feb 22. Neurobiol Aging. 2012. PMID: 22361451
281 results