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A novel mutation in a large French-Canadian family with LGMD1B.
Chrestian N, Valdmanis PN, Echahidi N, Brunet D, Bouchard JP, Gould P, Rouleau GA, Champagne J, Dupré N. Chrestian N, et al. Among authors: gould p. Can J Neurol Sci. 2008 Jul;35(3):331-4. doi: 10.1017/s031716710000891x. Can J Neurol Sci. 2008. PMID: 18714801
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: gould p. Acta Neuropathol Commun. 2015 Jan 31;3:5. doi: 10.1186/s40478-014-0181-z. Acta Neuropathol Commun. 2015. PMID: 25637145 Free PMC article.
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis.
Paré B, Lehmann M, Beaudin M, Nordström U, Saikali S, Julien JP, Gilthorpe JD, Marklund SL, Cashman NR, Andersen PM, Forsberg K, Dupré N, Gould P, Brännström T, Gros-Louis F. Paré B, et al. Among authors: gould p. Sci Rep. 2018 Sep 21;8(1):14223. doi: 10.1038/s41598-018-31773-z. Sci Rep. 2018. PMID: 30242181 Free PMC article.
298 results