17 results
P.043 Developing a brief clinical dataset for Duchenne Muscular Dystrophy
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- Canadian Journal of Neurological Sciences / Volume 51 / Issue s1 / June 2024
- Published online by Cambridge University Press:
- 24 May 2024, p. S27
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P.058 Neuromuscular neurologists’ experience in recognizing, diagnosing, and treating Long-chain fatty acid disorders (LC-FAOD): a national survey
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- Canadian Journal of Neurological Sciences / Volume 51 / Issue s1 / June 2024
- Published online by Cambridge University Press:
- 24 May 2024, p. S32
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P.046 Real-world survival effectiveness of edaravone in amyotrophic lateral sclerosis: a propensity score weighted, registry-based, Canada-wide cohort study
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- Canadian Journal of Neurological Sciences / Volume 50 / Issue s2 / June 2023
- Published online by Cambridge University Press:
- 05 June 2023, p. S70
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P.084 The Canadian Neuromuscular Disease Registry: a national spinal muscular atrophy registry for real world evidence
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- Canadian Journal of Neurological Sciences / Volume 50 / Issue s2 / June 2023
- Published online by Cambridge University Press:
- 05 June 2023, p. S81
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P.073 Mapping a national Duchenne muscular dystrophy registry to the International Classification of Functioning, Disability, and Health
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- Canadian Journal of Neurological Sciences / Volume 50 / Issue s2 / June 2023
- Published online by Cambridge University Press:
- 05 June 2023, p. S78
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P.036 Are there sex differences in the treatment of myasthenia gravis? a single centre cohort study
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- Canadian Journal of Neurological Sciences / Volume 50 / Issue s2 / June 2023
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- 05 June 2023, p. S67
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P.084 5q spinal muscular atrophy Canadian Paediatric Surveillance Program – 2020-2021 results
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- Canadian Journal of Neurological Sciences / Volume 49 / Issue s1 / June 2022
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- 24 June 2022, pp. S29-S30
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P.047 Implications of Gold Coast Criteria in diagnosis of amyotrophic lateral sclerosis in a large subspecialty clinic
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- Canadian Journal of Neurological Sciences / Volume 49 / Issue s1 / June 2022
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- 24 June 2022, p. S20
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GP.3 Measurement of decremental response is repeatable in amyotrophic lateral sclerosis
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- Canadian Journal of Neurological Sciences / Volume 49 / Issue s1 / June 2022
- Published online by Cambridge University Press:
- 24 June 2022, p. S1
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P.112 5q Spinal Muscular Atrophy Canadian Paediatric Surveillance Program - 2020 Results
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- Canadian Journal of Neurological Sciences / Volume 48 / Issue s3 / November 2021
- Published online by Cambridge University Press:
- 05 January 2022, pp. S50-S51
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Response to Provincial Governments’ Decisions Regarding Monitoring for Adults with Spinal Muscular Atrophy
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- Canadian Journal of Neurological Sciences / Volume 48 / Issue 2 / March 2021
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- 27 July 2020, pp. 201-203
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A National Spinal Muscular Atrophy Registry for Real-World Evidence
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- Canadian Journal of Neurological Sciences / Volume 47 / Issue 6 / November 2020
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- 04 June 2020, pp. 810-815
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Provincial Differences in the Diagnosis and Care of Amyotrophic Lateral Sclerosis
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- Canadian Journal of Neurological Sciences / Volume 45 / Issue 6 / November 2018
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- 15 November 2018, pp. 652-659
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P.071 Novel mutations in SPG7 identified from patients with late-onset spasticity
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- Canadian Journal of Neurological Sciences / Volume 45 / Issue s2 / June 2018
- Published online by Cambridge University Press:
- 27 June 2018, p. S35
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Pompe Disease: Diagnosis and Management. Evidence-Based Guidelines from a Canadian Expert Panel
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- Canadian Journal of Neurological Sciences / Volume 43 / Issue 4 / July 2016
- Published online by Cambridge University Press:
- 08 April 2016, pp. 472-485
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The CNDR: Collaborating to Translate New Therapies for Canadians
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- Canadian Journal of Neurological Sciences / Volume 40 / Issue 5 / September 2013
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- 23 September 2014, pp. 698-704
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Establishing a Canadian Registry of Patients with Amyotrophic Lateral Sclerosis
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- Canadian Journal of Neurological Sciences / Volume 40 / Issue 1 / January 2013
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- 23 September 2014, pp. 29-35
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