ArticleFrontiers in human neuroscience2022
Longitudinal Alterations in Gait Features in Growing Children With Duchenne Muscular Dystrophy.
Article in Frontiers in human neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 21 citations in OpenAlex.
- Wearable sensors for trunk posture monitoring in Duchenne muscular dystrophy: a case study.Medical & biological engineering & computing · 2026Article
- Gait analysis reveals new outcome measures for monitoring disease progression in individuals with late-onset Pompe disease.Journal of neuroengineering and rehabilitation · 2026Article
- Compensation for balance disorders: analysis of this multifactorial process.European journal of translational myology · 2025Article
- Longitudinal interaction between muscle impairments and gait pathology in growing children with Duchenne muscular dystrophy.Journal of neuroengineering and rehabilitation · 2025Observational
- Spinal Sagittal Alignment Assessment and Hip Range of Motion in Ambulatory Boys with Duchenne Muscular Dystrophy: Reliability, Diagnosis and Implications for Physiotherapy Management.Healthcare (Basel, Switzerland) · 2025Article
- Muscle weakness but also contractures contribute to the progressive gait pathology in children with Duchenne muscular dystrophy: a simulation study.Journal of neuroengineering and rehabilitation · 2025Article
- Longitudinal trajectories of muscle impairments in growing boys with Duchenne muscular dystrophy.PloS one · 2025Article
- Gait classification for growing children with Duchenne muscular dystrophy.Scientific reports · 2024Article
- Population longitudinal analysis of Gait Profile Score and North Star Ambulatory Assessment in children with Duchenne muscular dystrophy.CPT: pharmacometrics & systems pharmacology · 2024Article
- Gait asymmetry in children with Duchenne muscular dystrophy: evaluated through kinematic synergies and muscle synergies of lower limbs.Biomedical engineering online · 2023Article
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Authors and funding
12 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Prolonging ambulation is an important treatment goal in children with Duchenne muscular dystrophy (DMD). Three-dimensional gait analysis (3DGA) could provide sensitive parameters to study the efficacy of clinical trials aiming to preserve ambulation. However, quantitative descriptions of the natural history of gait features in DMD are first required. The overall goal was to provide a full delineation of the progressive gait pathology in children with DMD, covering the entire period of ambulation, by performing a so-called mixed cross-sectional longitudinal study. Firstly, to make our results comparable with previous literature, we aimed to cross-sectionally compare 31 predefined gait features between children with DMD and a typically developing (TD) database (1). Secondly, we aimed to explore the longitudinal changes in the 31 predefined gait features in growing boys with DMD using follow-up 3DGA sessions (2). 3DGA-sessions (
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