Gould P - Search Results

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: 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.

2

From animal models to human disease: a genetic approach for personalized medicine in ALS.

Picher-Martel V, Valdmanis PN, Gould PV, Julien JP, Dupré N. Picher-Martel V, et al. Acta Neuropathol Commun. 2016 Jul 11;4(1):70. doi: 10.1186/s40478-016-0340-5. Acta Neuropathol Commun. 2016. PMID: 27400686 Free PMC article. Review.

3

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.

4

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

5

Recent studies on oculopharyngeal muscular dystrophy in Québec.

Bouchard JP, Brais B, Brunet D, Gould PV, Rouleau GA. Bouchard JP, et al. Among authors: gould pv. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S22-9. doi: 10.1016/s0960-8966(97)00077-1. Neuromuscul Disord. 1997. PMID: 9392011

6

Intravascular lymphoma with conus medullaris syndrome followed by encephalopathy.

Savard M, Verreault S, Gould PV, Bernier V, Bouchard JP. Savard M, et al. Can J Neurol Sci. 2008 Jul;35(3):366-71. doi: 10.1017/s0317167100008982. Can J Neurol Sci. 2008. PMID: 18714808 Review.

7

A case of familial Creutzfeldt-Jakob disease presenting with dry cough.

Larue S, Verreault S, Gould P, Coulthart MB, Bergeron C, Dupré N. Larue S, et al. Among authors: gould p. Can J Neurol Sci. 2006 May;33(2):243-5. doi: 10.1017/s0317167100005072. Can J Neurol Sci. 2006. PMID: 16736740

8

Creutzfeldt-Jakob Disease-Like Periodic Sharp Wave Complexes in Voltage-Gated Potassium Channel-Complex Antibodies Encephalitis: A Case Report.

Savard M, Irani SR, Guillemette A, Gosselin-Lefebvre S, Geschwind M, Jansen GH, Gould PV, Laforce R Jr. Savard M, et al. J Clin Neurophysiol. 2016 Feb;33(1):e1-4. doi: 10.1097/WNP.0000000000000171. J Clin Neurophysiol. 2016. PMID: 26375660 Free PMC article.

9

Perforated duodenal ulcer in a pediatric patient with eosinophilic gastroenteritis.

Deslandres C, Russo P, Gould P, Hardy P. Deslandres C, et al. Among authors: gould p. Can J Gastroenterol. 1997 Apr;11(3):208-12. doi: 10.1155/1997/809363. Can J Gastroenterol. 1997. PMID: 9167027 Review.

10

Gap junctions in human glioblastomas: implications for suicide gene therapy.

Cottin S, Gould PV, Cantin L, Caruso M. Cottin S, et al. Among authors: gould pv. Cancer Gene Ther. 2011 Sep;18(9):674-81. doi: 10.1038/cgt.2011.38. Epub 2011 Jul 22. Cancer Gene Ther. 2011. PMID: 21779029

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