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 > MYOBASE > BIOLOGIE > biologie par appareil > appareil locomoteur > physiologie locomotrice > motricité
motricitéSynonyme(s)motor activity ;motoricity ;motricity ;activité motrice ;fonction motrice motor functionVoir aussi |
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Recombinant human insulin-like growth factor-1 (rhIGF-1) therapy for six months improves growth but not motor function in boys with Duchenne Muscular Dystrophy
Rutter MM, Wong BL, Collins JJ, et al.
Muscle & Nerve, 2020
Scoliosis Surgery Significantly Impacts Motor Abilities in Higher-functioning Individuals with Spinal Muscular Atrophy
Dunaway-Young S, Montes J, Salazar R, et al.
Journal of Neuromuscular Diseases, 2020
A Case Study With Symbihand: An sEMG-Controlled Electrohydraulic Hand Orthosis for Individuals With Duchenne Muscular Dystrophy
Bos RA, Nizamis K, Koopman BFJM, et al.
IEEE Transactions on neural systems and rehabilitation engineering, 2020, 28, 1, p 258
Evaluation of the cognitive-motor performance of adults with Duchenne Muscular Dystrophy in a hand-related task
Nizamis K, Schutte W, Grutters JJ, et al.
PLoS ONE, 2020, 15, 1
Evaluation of speed-accuracy trade-off in a computer task to identify motor difficulties in individuals with Duchenne Muscular Dystrophy - A cross-sectional study
da Silva TD, Ribeiro-Papa DC, Coe S, et al.
Research in developmental disabilities, 2020, 96
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
Measuring walking-related performance fatigability in clinical practice: a systematic review
Van Geel F, Moumdjian L, Lamers I, et al.
European journal of physical and rehabilitation medicine, 2019
Effect of Combination l-Citrulline and Metformin Treatment on Motor Function in Patients With Duchenne Muscular Dystrophy: A Randomized Clinical Trial
Hafner P, Bonati U, Klein A, et al.
JAMA network open, 2019, 2, 10
Motor activity and Becker's muscular dystrophy: lights and shadows
Lanza G, Pino M, Fisicaro F, et al.
The Physician and sportsmedicine, 2019
Categorising trajectories and individual item changes of the North Star Ambulatory Assessment in patients with Duchenne muscular dystrophy
Muntoni F, Domingos J, Manzur AY, et al.
PLoS ONE, 2019, 14, 9
Home-Based Monitor for Gait and Activity Analysis
Lilien C, Gasnier E, Gidaro T, et al.
Journal of visualized experiments : JoVE, 2019, n 150
Motor learning from virtual reality to natural environments in individuals with Duchenne muscular dystrophy
Quadrado VH, Silva TDD, Favero FM, et al.
Disability and rehabilitation. Assistive technology, 2019, 14, 1, p 12
Long-term follow-up of 17 patients with childhood Pompe disease treated with enzyme replacement therapy
van der Meijden JC, Kruijshaar ME, Harlaar L, et al.
Journal of inherited metabolic disease, 2018
Functional outcome measures for infantile Charcot-Marie-Tooth disease: a systematic review
Mandarakas MR, Rose KJ, Sanmaneechai O, et al.
Journal of the peripheral nervous system : JPNS, 2018
Severe cognitive impairment in a patient with CMT2A
Tomaselli PJ, Kapoor M, Cortese A, et al.
Journal of the peripheral nervous system : JPNS, 2018
Membre supérieur : Ne Baissez pas les bras sur les aides techniques
Robert-Géraude A, Fattal C
Faire face, 2018, 754, p. 12-14
Myopathie de Duchenne association gagnante L-citrulline et metformine : La recherche En bref
Dupuy-Maury F
VLM. Vaincre les myopathies, 2018, 184, p. 26
