Detalhe da pesquisa
1.
A Study on the Incidence and Prevalence of 5q Spinal Muscular Atrophy in Canada Using Multiple Data Sources.
Can J Neurol Sci
; : 1-12, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38178730
2.
Motor cortex functional connectivity is associated with underlying neurochemistry in ALS.
J Neurol Neurosurg Psychiatry
; 94(3): 193-200, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36379713
3.
Distinct patterns of progressive gray and white matter degeneration in amyotrophic lateral sclerosis.
Hum Brain Mapp
; 43(5): 1519-1534, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34908212
4.
Gold Coast criteria expand clinical trial eligibility in amyotrophic lateral sclerosis.
Muscle Nerve
; 66(4): 397-403, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35673968
5.
Randomized phase 2 study of ACE-083, a muscle-promoting agent, in facioscapulohumeral muscular dystrophy.
Muscle Nerve
; 66(1): 50-62, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35428982
6.
Utility of Neuropathy Screening for Wild-Type Transthyretin Amyloidosis Patients.
Can J Neurol Sci
; 48(5): 607-615, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33342448
7.
A National Spinal Muscular Atrophy Registry for Real-World Evidence.
Can J Neurol Sci
; 47(6): 810-815, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32493524
8.
High diagnostic yield and novel variants in very late-onset spasticity.
J Neurogenet
; 33(1): 27-32, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30747022
9.
Provincial Differences in the Diagnosis and Care of Amyotrophic Lateral Sclerosis.
Can J Neurol Sci
; 45(6): 652-659, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30430962
10.
The Canadian Neuromuscular Disease Registry: Connecting patients to national and international research opportunities.
Paediatr Child Health
; 23(1): 20-26, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29479275
11.
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change.
Muscle Nerve
; 66(6): E34-E35, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36116127
12.
A Systematic Review and Meta-analysis on the Epidemiology of the Muscular Dystrophies.
Can J Neurol Sci
; 43(1): 163-77, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26786644
13.
Pompe Disease: Diagnosis and Management. Evidence-Based Guidelines from a Canadian Expert Panel.
Can J Neurol Sci
; 43(4): 472-85, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27055517
14.
Response to Provincial Governments' Decisions Regarding Monitoring for Adults with Spinal Muscular Atrophy.
Can J Neurol Sci
; 48(2): 201-203, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32713403
15.
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
Hum Mutat
; 36(4): 395-402, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25604253
16.
Profile of patients with amyotrophic lateral sclerosis across continuum of care.
Can J Neurol Sci
; 41(2): 246-52, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24534038
17.
Mismatch between clinically defined classification of ALS stage and the burden of cerebral pathology.
J Neurol
; 271(5): 2547-2559, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38282082
18.
The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia.
Hum Mutat
; 34(11): 1449-57, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23913485
19.
Perspectives on neurological patient registries: a literature review and focus group study.
BMC Med Res Methodol
; 13: 135, 2013 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-24209392
20.
Response to the Canadian Agency for Drugs and Technologies in Health and Institut national d'excellence en santé et en services sociaux decision regarding nusinersen for Spinal Muscular Atrophy.
Can J Neurol Sci
; 45(5): 516-517, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30039778