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Antoine Duquette
Antoine Duquette
Professeur agrégé de clinique, Université de Montréal
在 umontreal.ca 的电子邮件经过验证
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引用次数
引用次数
年份
Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy
A Duquette, K Roddier, J McNabb‐Baltar, I Gosselin, A St‐Denis, ...
Annals of neurology 57 (3), 408-414, 2005
1432005
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
D Pellerin, MC Danzi, C Wilke, M Renaud, S Fazal, MJ Dicaire, CK Scriba, ...
New England Journal of Medicine 388 (2), 128-141, 2023
1202023
Safety and efficacy of tilavonemab in progressive supranuclear palsy: a phase 2, randomised, placebo-controlled trial
GU Höglinger, I Litvan, N Mendonca, D Wang, H Zheng, ...
The Lancet Neurology 20 (3), 182-192, 2021
1152021
Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene
E Stumpf, H Masson, A Duquette, F Berthelet, J McNabb, A Lortie, ...
Archives of neurology 60 (9), 1307-1312, 2003
1152003
Clinical presentation and early evolution of spastic ataxia of Charlevoix‐Saguenay
A Duquette, B Brais, JP Bouchard, J Mathieu
Movement Disorders 28 (14), 2011-2014, 2013
662013
Diversity of ARSACS mutations in French-Canadians
I Thiffault, MJ Dicaire, M Tetreault, KN Huang, J Demers-Lamarche, ...
Canadian journal of neurological sciences 40 (1), 61-66, 2013
662013
Tau secretion: good and bad for neurons
C Pernègre, A Duquette, N Leclerc
Frontiers in neuroscience 13, 649, 2019
572019
Best practices in the clinical management of progressive supranuclear palsy and corticobasal syndrome: a consensus statement of the CurePSP Centers of Care
B Bluett, AY Pantelyat, I Litvan, F Ali, D Apetauerova, D Bega, L Bloom, ...
Frontiers in Neurology 12, 694872, 2021
502021
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21
M Tetreault, A Duquette, I Thiffault, C Bherer, J Jarry, L Loisel, B Banwell, ...
Brain 129 (8), 2077-2084, 2006
392006
Natural history of Friedreich ataxia: heterogeneity of neurologic progression and consequences for clinical trial design
C Rummey, LA Corben, M Delatycki, G Wilmot, SH Subramony, M Corti, ...
Neurology 99 (14), e1499-e1510, 2022
322022
Similarities and differences in the pattern of tau hyperphosphorylation in physiological and pathological conditions: impacts on the elaboration of therapies to prevent tau …
A Duquette, C Pernègre, A Veilleux Carpentier, N Leclerc
Frontiers in Neurology 11, 607680, 2021
302021
Familial congenital mirror movements: report of a large 4-generation family
M Srour, M Philibert, MH Dion, A Duquette, F Richer, GA Rouleau, ...
Neurology 73 (9), 729-731, 2009
252009
Tominersen in adults with manifest Huntington's disease
P McColgan, A Thobhani, L Boak, SA Schobel, A Nicotra, G Palermo, ...
The New England journal of medicine 389 (23), 2203-2205, 2023
242023
Worldwide barriers to genetic testing for movement disorders
EM Gatto, RH Walker, C Gonzalez, M Cesarini, G Cossu, CD Stephen, ...
European journal of neurology 28 (6), 1901-1909, 2021
222021
Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation
SA Nahas, A Duquette, K Roddier, RA Gatti, B Brais
Neuromuscular Disorders 17 (11-12), 968-969, 2007
172007
Clinical management guidelines for Friedreich ataxia: best practice in rare diseases
LA Corben, V Collins, S Milne, J Farmer, A Musheno, D Lynch, ...
Orphanet journal of rare diseases 17 (1), 415, 2022
162022
Scoliosis in Friedreich's ataxia: longitudinal characterization in a large heterogeneous cohort
C Rummey, JM Flynn, LA Corben, MB Delatycki, G Wilmot, ...
Annals of clinical and translational neurology 8 (6), 1239-1250, 2021
132021
Estimated prevalence of Niemann–Pick type C disease in Quebec
M Labrecque, L Touma, C Bhérer, A Duquette, M Tétreault
Scientific reports 11 (1), 22621, 2021
92021
Whipple's disease presenting with segmental myoclonus and hypersomnia
C Xia, A Duquette, S Frucht, AL Lafontaine
Movement disorders 27 (10), 1216-1217, 2012
82012
The neurophysiological brain-fingerprint of Parkinson’s disease
J da Silva Castanheira, AI Wiesman, JY Hansen, B Misic, S Baillet, ...
EBioMedicine 105, 2024
52024
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