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Growth assessment and weight management in paediatric neuromuscular clinics: a cross-sectional survey across Canada
McPherson AC, Amin R, McAdam L, et al.
Disability and rehabilitation, 2020
Daily activity performance in congenital and childhood forms of myotonic dystrophy type 1: a population-based study
Eriksson BM, Ekstrom AB, Peny-Dahlstrand M
Developmental medicine and child neurology, 2019
Patient-Reported Prevalence of Non-motor Symptoms Is Low in Adult Patients Suffering From 5q Spinal Muscular Atrophy
Gunther R, Wurster CD, Cordts I, et al.
Frontiers in neurology, 2019, 10, 1098
Monitoring daily physical activity of upper extremity in young and adolescent boys with Duchenne muscular dystrophy: A pilot study
van der Geest A, Essers JMN, Bergsma A, et al.
Muscle & Nerve, 2019
Use of a wearable device to assess sleep and motor function in Duchenne muscular dystrophy
Siegel BI, Cakmak A, Reinertsen E, et al.
Muscle & Nerve, 2019
Reproductive Cancer Risk Factors in Women With Myotonic Dystrophy (DM): Survey Data From the US and UK DM Registries
Higgs C, Hilbert JE, Wood L, et al.
Frontiers in neurology, 2019, 10, p 1071
Clinical and Molecular Disease Spectrum and Outcomes in Patients with Infantile-Onset Pompe Disease
Gupta N, Kazi ZB, Nampoothiri S, et al.
The Journal of pediatrics, 2019
Prevalence and Associated Factors of Depressive Symptoms in Patients with Myasthenia Gravis: A Cross-Sectional Study of Two Tertiary Hospitals in Riyadh, Saudi Arabia
Alanazy MH
Behavioural neurology, 2019
Psychosocial adjustment and parental stress in Duchenne Muscular Dystrophy
Gocheva V, Schmidt S, Orsini AL, et al.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2019
Cross-Sectional Analysis of the Myasthenia Gravis Patient Registry: Disability and Treatment
Cutter G, Xin H, Aban I, et al.
Muscle & Nerve, 2019
Patient-reported disease burden in oculopharyngeal muscular dystrophy
Kurtz NS, Côte C, Heatwole C, et al.
Muscle & Nerve, 2019
Nailfold videocapillaroscopy alterations in dermatomyositis, antisynthetase syndrome, overlap myositis, and immune-mediated necrotizing myopathy
Soubrier C, Seguier J, Di Costanzo MP, et al.
Clinical rheumatology, 2019
The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
Thangarajh M, Kaat AJ, Bibat G, et al.
Annals of clinical and translational neurology, 2019, 6, 9, p 1696
Growth and differentiation factor 15 as a biomarker for mitochondrial myopathy
Poulsen NS, Madsen KL, Hornsyld TM, et al.
Mitochondrion, 2019, 50, p 35
Muscle contractility of leg muscles in patients with mitochondrial myopathies
Poulsen NS, Poulsen NS, Dahlqvist JR, et al.
Mitochondrion, 2018
It's not just physical: a qualitative study regarding the illness experiences of people with facioscapulohumeral muscular dystrophy
Bakker M, Schipper K, Geurts AC, et al.
Disability and rehabilitation, 2017, 39, 10, p 978
Active lung volume recruitment to preserve vital capacity in Duchenne muscular dystrophy
Chiou M, Bach JR, Jethani L, et al.
Journal of rehabilitation medicine, 2017, 49, 1, p 49
Myopathie de Duchenne et constipation : une association fréquente et souvent négligée
Urtizberea JA
2016
Dystrophie musculaire de Duchenne : l'analyse quantifiée de la marche reste un outil de mesure performant
Urtizberea JA
2016
Dystrophie musculaire oculopharyngée : phénomène de fatigue et de douleur souvent négligés
Urtizberea JA
2016
