Antoine Duquette - Publications

Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States 
Neurogenetics, neurodegenerative disorders, Parkinson's disease, hereditary ataxias

9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Bernier A, Dorais J, Gagnon B, Lepage C, Jodoin N, Soland V, Panisset M, Chouinard S, Duquette A. Enteral Feeding Using Levodopa-Carbidopa Intestinal Gel Percutaneous Endoscopic Gastrostomy Tube. Movement Disorders Clinical Practice. 4: 787-788. PMID 30838290 DOI: 10.1002/mdc3.12490  0.36
2013 Duquette A, Brais B, Bouchard JP, Mathieu J. Clinical presentation and early evolution of spastic ataxia of Charlevoix-Saguenay. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 2011-4. PMID 23913799 DOI: 10.1002/mds.25604  0.52
2013 Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, et al. Diversity of ARSACS mutations in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 61-6. PMID 23250129  0.52
2012 Xia C, Duquette A, Frucht S, Lafontaine AL. Whipple's disease presenting with segmental myoclonus and hypersomnia. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1216-7. PMID 22976777 DOI: 10.1002/mds.24039  0.52
2009 Srour M, Philibert M, Dion MH, Duquette A, Richer F, Rouleau GA, Chouinard S. Familial congenital mirror movements: report of a large 4-generation family. Neurology. 73: 729-31. PMID 19720981 DOI: 10.1212/WNL.0b013e3181b59bda  0.36
2007 Nahas SA, Duquette A, Roddier K, Gatti RA, Brais B. Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation. Neuromuscular Disorders : Nmd. 17: 968-9. PMID 17720498 DOI: 10.1016/j.nmd.2007.06.464  0.52
2006 Tétreault M, Duquette A, Thiffault I, Bherer C, Jarry J, Loisel L, Banwell B, D'Anjou G, Mathieu J, Robitaille Y, Vanasse M, Brais B. A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21. Brain : a Journal of Neurology. 129: 2077-84. PMID 16760198 DOI: 10.1093/brain/awl146  0.52
2005 Duquette A, Roddier K, McNabb-Baltar J, Gosselin I, St-Denis A, Dicaire MJ, Loisel L, Labuda D, Marchand L, Mathieu J, Bouchard JP, Brais B. Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy. Annals of Neurology. 57: 408-14. PMID 15732101 DOI: 10.1002/ana.20408  0.52
2003 Stumpf E, Masson H, Duquette A, Berthelet F, McNabb J, Lortie A, Lesage J, Montplaisir J, Brais B, Cossette P. Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene. Archives of Neurology. 60: 1307-12. PMID 12975300 DOI: 10.1001/archneur.60.9.1307  0.52
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