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Psychometric Characteristics of the Motor Function Measure in Neuromuscular Diseases: A Systematic Review<sup>1</sup>.
- Published in:
- Journal of Neuromuscular Diseases, 2023, v. 10, n. 3, p. 301, doi. 10.3233/JND-230001
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- Article
E-Health & Innovation to Overcome Barriers in Neuromuscular Diseases. Report from the 1st eNMD Congress: Nice, France, March 22-23, 2019.
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- Journal of Neuromuscular Diseases, 2021, v. 8, n. 4, p. 743, doi. 10.3233/JND-210655
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- Article
Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA study.
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- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0201004
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- Article
Understanding the relationship between the 32-item motor function measure and daily activities from an individual with spinal muscular atrophy and their caregivers' perspective: a two-part study.
- Published in:
- 2021
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- Publication type:
- journal article
Natural history of Type 2 and 3 spinal muscular atrophy: 2‐year NatHis‐SMA study.
- Published in:
- Annals of Clinical & Translational Neurology, 2021, v. 8, n. 2, p. 359, doi. 10.1002/acn3.51281
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- Article
Correction to: Two‑year efficacy and safety of risdiplam in patients with type 2 or non‑ambulant type 3 spinal muscular atrophy (SMA).
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- 2023
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- Correction Notice
Two-year efficacy and safety of risdiplam in patients with type 2 or non-ambulant type 3 spinal muscular atrophy (SMA).
- Published in:
- Journal of Neurology, 2023, v. 270, n. 5, p. 2531, doi. 10.1007/s00415-023-11560-1
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- Article
Correction to: Use of MFM-20 to monitor SMA types 1 and 2 patients treated with nusinersen.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Use of MFM-20 to monitor SMA types 1 and 2 patients treated with nusinersen.
- Published in:
- Neurological Sciences, 2023, v. 44, n. 1, p. 329, doi. 10.1007/s10072-022-06403-2
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- Article
Assessment of the validity and reliability of the 32-item Motor Function Measure in individuals with Type 2 or non-ambulant Type 3 spinal muscular atrophy.
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- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0238786
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- Article
Perceived impact of lockdown on daily life in children with physical disabilities and their families during the COVID‐19 pandemic.
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- Child: Care, Health & Development, 2022, v. 48, n. 6, p. 942, doi. 10.1111/cch.12952
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- Article
Confirmatory validation of the french version of the Duchenne Muscular Dystrophy module of the pediatric quality of life inventory (PedsQL<sup>TM</sup>3.0DMDfv).
- Published in:
- BMC Pediatrics, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12887-023-04153-4
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- Article
Muscle Activation during Gait in Children with Duchenne Muscular Dystrophy.
- Published in:
- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0161938
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- Article
Respiratory management of spinal muscular atrophy type 1 patients treated with Nusinersen.
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- Pediatric Pulmonology, 2022, v. 57, n. 6, p. 1505, doi. 10.1002/ppul.25899
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- Publication type:
- Article
Validity and Reliability of the 32-Item Motor Function Measure in 2- to 5-Year-Olds with Neuromuscular Disorders and 2- to 25-Year-Olds with Spinal Muscular Atrophy.
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- Neurology & Therapy, 2020, v. 9, n. 2, p. 575, doi. 10.1007/s40120-020-00206-3
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- Article
ADEQUATE TRANSITION OF HEALTH CARE FROM CHILD TO ADULT FOR PATIENTS WITH MOTOR DISABILITY: ENVIRONMENTAL, MEDICAL AND SOCIAL CHALLENGES.
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- Journal of Rehabilitation Medicine (Stiftelsen Rehabiliteringsinformation), 2015, v. 47, n. 8, p. 769
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- Article
SMA: Des échelles d'évaluation motrice pour le public francophone.
- Published in:
- Médecine Sciences, 2019, v. 35, p. 24, doi. 10.1051/medsci/2019189
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- Publication type:
- Article
SMA: Des échelles d’évaluation motrice pour le public francophone.
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- Médecine Sciences, 2019, v. 35, p. 24, doi. 10.1051/medsci/2019189
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- Article
Critères de jugement pour les essais cliniques dans les maladies neuromusculaires.
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- Médecine Sciences, 2018, v. 34, p. 49, doi. 10.1051/medsci/201834s216
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- Article
La juste mesure pour un meilleur accompagnement.
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- Médecine Sciences, 2017, v. 33, p. 5, doi. 10.1051/medsci/201733s101
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- Article
Elementary visuospatial perception deficit in children with neurodevelopmental disorders.
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- Developmental Medicine & Child Neurology, 2021, v. 63, n. 4, p. 457, doi. 10.1111/dmcn.14743
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- Publication type:
- Article
Corticosteroids in Duchenne muscular dystrophy: impact on the motor function measure sensitivity to change and implications for clinical trials.
- Published in:
- 2018
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- Publication type:
- journal article
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure.
- Published in:
- Developmental Medicine & Child Neurology, 2010, v. 52, n. 1, p. 60, doi. 10.1111/j.1469-8749.2009.03316.x
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- Publication type:
- Article
Correction to: Understanding the relationship between the 32-item motor function measure and daily activities from an individual with spinal muscular atrophy and their caregivers' perspective: a two-part study.
- Published in:
- 2021
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- Publication type:
- corrected article
Understanding the relationship between the 32-item motor function measure and daily activities from an individual with spinal muscular atrophy and their caregivers' perspective: a two-part study.
- Published in:
- BMC Neurology, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12883-021-02166-z
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- Publication type:
- Article
Understanding the relationship between the 32-item motor function measure and daily activities from an individual with spinal muscular atrophy and their caregivers' perspective: a two-part study.
- Published in:
- BMC Neurology, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12883-021-02166-z
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- Publication type:
- Article
Effects of nusinersen after one year of treatment in 123 children with SMA type 1 or 2: a French real-life observational study.
- Published in:
- 2020
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- Publication type:
- journal article
Motor function performance in individuals with RYR1-related myopathies.
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- 2019
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- Publication type:
- journal article
Mathematical Disease Progression Modeling in Type 2/3 Spinal Muscular Atrophy.
- Published in:
- 2018
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- Publication type:
- journal article
Electrical impedance myography in individuals with collagen 6 and laminin α-2 congenital muscular dystrophy: a cross-sectional and 2-year analysis.
- Published in:
- 2018
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- Publication type:
- journal article
A Patient-Centered Evaluation of Meaningful Change on the 32-Item Motor Function Measure in Spinal Muscular Atrophy Using Qualitative and Quantitative Data.
- Published in:
- Frontiers in Neurology, 2022, p. 1, doi. 10.3389/fneur.2021.770423
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- Publication type:
- Article
Risdiplam in types 2 and 3 spinal muscular atrophy: A randomised, placebo‐controlled, dose‐finding trial followed by 24 months of treatment.
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- European Journal of Neurology, 2023, v. 30, n. 7, p. 1945, doi. 10.1111/ene.15499
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- Publication type:
- Article
Early Intensive Bimanual Stimulation Program (BB-Bim) for Infants at Risk of Unilateral Cerebral Palsy: A Randomized, Multiple-Baseline, Single-Case Study.
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- American Journal of Occupational Therapy, 2023, v. 77, n. 6, p. 1, doi. 10.5014/ajot.2023.050232
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- Article