Nathalie Goemans

University of Calgary — Canada

Biochemistry, Genetics and Molecular Biology · Life Sciences

54h-index11.2kcitations290works8.82yr avg
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Research Topics

Muscle Physiology and Disorders(154), Neurogenetic and Muscular Disorders Research(93), Cardiomyopathy and Myosin Studies(40), Children's Physical and Motor Development(31), Muscle activation and electromyography studies(29)

Publications285 total

Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patients.
Scientific Reports·2025· 1 citedOpen Access
Re-evaluating acceptable risk of death from gene therapy: A threshold study among individuals with Duchenne muscular dystrophy and their caregivers in the US and UK
European Journal of Medical Genetics·2025Open Access
Longitudinal interaction between muscle impairments and gait pathology in growing children with Duchenne muscular dystrophy
Journal of NeuroEngineering and Rehabilitation·2025Open Access
Descriptive characterization of ambulatory health states in Duchenne muscular dystrophy: Motor function trajectories and times to loss of ambulation
Journal of Neuromuscular Diseases·2025Open Access
Development of the Accredited Duchenne Centers Program, a Global Program to Achieve Uniform and Up-to-date Care for All People Living with Duchenne Muscular Dystrophy
Journal of Rehabilitation Therapy·2025Open Access
Longitudinal relation between muscle impairments and gait pathology in growing boys with Duchenne muscular dystrophy
Gait & Posture·2025
Development of the accredited duchenne centers program, a global program to achieve uniform and up-to-date care for all people living with duchenne muscular dystrophy
Orphanet Journal of Rare Diseases·2025Open Access
Predicting trajectories of the north star ambulatory assessment total score in Duchenne muscular dystrophy
PLoS ONE·2025· 2 citedOpen Access
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·2025· 1 citedOpen Access
Longitudinal trajectories of muscle impairments in growing boys with Duchenne muscular dystrophy
PLoS ONE·2025· 3 citedOpen Access
Development of the Accredited Duchenne Centers Program, a global program to achieve uniform and up-to-date care for all people living with Duchenne Muscular Dystrophy
2025Open Access
Muscle weakness but also contractures contribute to the progressive gait pathology in children with DMD: a simulation study
2025· 2 citedOpen Access
Longitudinal interaction between muscle impairments and gait pathology in growing children with Duchenne muscular dystrophy
2024· 4 citedOpen Access
Evidentiary basis of the first regulatory qualification of a digital primary efficacy endpoint
Scientific Reports·2024· 17 citedOpen Access
Genotype and corticosteroid treatment are distinctively associated with gray matter characteristics in patients with Duchenne muscular dystrophy
Neuromuscular Disorders·2024· 2 citedOpen Access
Characterization of patients with Duchenne muscular dystrophy across previously developed health states
PLoS ONE·2024· 5 citedOpen Access
How do fine and gross motor skills develop in preschool boys with Duchenne Muscular Dystrophy?
Research in Developmental Disabilities·2024· 2 citedOpen Access
Longitudinal trajectories of muscle strength deficits in growing boys with Duchenne muscular dystrophy
Gait & Posture·2024
Meaningful changes in motor function in Duchenne muscular dystrophy (DMD): A multi-center study
PLoS ONE·2024· 10 citedOpen Access
Early motor, cognitive, language, behavioural and social emotional development in infants and young boys with Duchenne Muscular Dystrophy- A systematic review
European Journal of Paediatric Neurology·2024· 6 citedOpen Access
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Frequent Co-authors

Eugenio Mercuri(21), Enrico Bertini(16), Gunnar Buyse(14), Craig M. McDonald(13), Richard S. Finkel(13), Janbernd Kirschner(12), Ulrike Schara(12), M. van den Hauwe(12), Elena Mazzone(10), Laurent Servais(9), Juan J. Vílchez(8), Thomas Voït(8), Giacomo P. Comi(8), M. Tulinius(7), Susan T. Iannaccone(7), Marika Pane(7), Nicolas Deconinck(7), Giovanni Baranello(7), Francesco Muntoni(6), Thomas Sejersen(6)