A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment
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Thomas Voit | David Vissière | Jean-Yves Hogrel | Eric Dorveaux | Laurent Servais | D. Vissière | L. Servais | J. Hogrel | T. Voit | A. Le Moing | Amélie Moraux | Erwan Gasnier | Anne-Gaëlle Le Moing | Andreea Mihaela Seferian | Mélanie Annoussamy | M. Annoussamy | A. Moraux | A. Seferian | K. Kajitani | E. Gasnier | T. Matsushita | E. Dorveaux | Ikumi Higashijima | Hideaki Fukumori | Kosuke Kaneko | Daewoong Kim | Laurent Servais | Thomas Voit | Anne-Gaëlle Le Moing | Mélanie Annoussamy | Erwan Gasnier
[1] A. Emery. Population frequencies of inherited neuromuscular diseases—A world survey , 1991, Neuromuscular Disorders.
[2] Elske Ammenwerth,et al. Measurement and quantification of generalized tonic–clonic seizures in epilepsy patients by means of accelerometry—An explorative study , 2011, Epilepsy Research.
[3] C. McDonald. Physical activity, health impairments, and disability in neuromuscular disease. , 2002, American journal of physical medicine & rehabilitation.
[4] Fabiana Luisa Mattar,et al. Hand weakness in Duchenne muscular dystrophy and its relation to physical disability , 2008, Neuromuscular Disorders.
[5] M. Grootenhuis,et al. Living with muscular dystrophy: health related quality of life consequences for children and adults , 2007, Health and quality of life outcomes.
[6] R. Carson,et al. Upper vs lower extremity functional loss in neuromuscular disease. , 1987, Archives of physical medicine and rehabilitation.
[7] V. Ricotti,et al. Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory, randomised, placebo-controlled phase 2 study , 2014, The Lancet Neurology.
[8] Nicolas Petit,et al. Iterative calibration method for inertial and magnetic sensors , 2009, Proceedings of the 48h IEEE Conference on Decision and Control (CDC) held jointly with 2009 28th Chinese Control Conference.
[9] John L. Crassidis,et al. Survey of nonlinear attitude estimation methods , 2007 .
[10] Pierre J. M. Cluitmans,et al. Detection of Subtle Nocturnal Motor Activity From 3-D Accelerometry Recordings in Epilepsy Patients , 2007, IEEE Transactions on Biomedical Engineering.
[11] F. Horak,et al. Assessing mobility at home in people with early Parkinson's disease using an instrumented Timed Up and Go test. , 2011, Parkinsonism & related disorders.
[12] Ilaria Carpinella,et al. Quantitative assessment of upper limb motor function in Multiple Sclerosis using an instrumented Action Research Arm Test , 2014, Journal of NeuroEngineering and Rehabilitation.
[13] P. Zimetbaum,et al. Ambulatory arrhythmia monitoring: choosing the right device. , 2010, Circulation.
[14] Brian W. Timmons,et al. Accelerometry: A Feasible Method to Quantify Physical Activity in Ambulatory and Nonambulatory Adolescents with Cerebral Palsy , 2012, International journal of pediatrics.
[15] Ruzena Bajcsy,et al. Validity, Reliability, and Sensitivity of a 3D Vision Sensor-based Upper Extremity Reachable Workspace Evaluation in Neuromuscular Diseases , 2013, PLoS currents.
[16] L. Servais,et al. Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy , 2016, Neurology.
[17] Vincent Bonnet,et al. Estimate of lower trunk angles in pathological gaits using gyroscope data. , 2013, Gait & posture.
[18] Philippe Kahane,et al. Classification of epileptic motor manifestations using inertial and magnetic sensors , 2011, Comput. Biol. Medicine.
[19] Roslyn N. Boyd,et al. Validity of accelerometry in ambulatory children and adolescents with cerebral palsy , 2011, European Journal of Applied Physiology.
[20] J. Fermanian,et al. [A motor function measurement scale for neuromuscular diseases - description and validation study]. , 2006, Revue neurologique.
[21] R. Abresch,et al. Utility of a step activity monitor for the measurement of daily ambulatory activity in children. , 2005, Archives of physical medicine and rehabilitation.
[22] Kun-Chan Lan,et al. On Calibrating the Sensor Errors of a PDR-Based Indoor Localization System , 2013, Sensors.
[23] L. Hiller,et al. Upper extremity functional assessment scales in children with Duchenne muscular dystrophy: a comparison. , 1992, Archives of physical medicine and rehabilitation.
[24] Carole Bérard,et al. La mesure de fonction motrice, outil d’évaluation clinique des maladies neuromusculaires. Étude de validation , 2006 .
[25] D. Escolar,et al. Clinical evaluator reliability for quantitative and manual muscle testing measures of strength in children , 2001, Muscle & nerve.
[26] J. Mendell,et al. Eteplirsen for the treatment of Duchenne muscular dystrophy , 2013, Annals of neurology.
[27] Sean Pearson,et al. Continuous Monitoring of Turning in Patients with Movement Disability , 2013, Sensors.
[28] C. Vandelanotte,et al. Socio-demographic factors and neighbourhood social cohesion influence adults’ willingness to grant children greater independent mobility: A cross-sectional study , 2015, BMC Public Health.
[29] R. Motl,et al. Real-life walking impairment in multiple sclerosis: preliminary comparison of four methods for processing accelerometry data , 2010, Multiple sclerosis.
[30] G. van Ommen,et al. Systemic administration of PRO051 in Duchenne's muscular dystrophy. , 2011, The New England journal of medicine.
[31] Domenico Formica,et al. A New Calibration Methodology for Thorax and Upper Limbs Motion Capture in Children Using Magneto and Inertial Sensors , 2014, Sensors.
[32] Kamiar Aminian,et al. Gait Assessment in Children With Duchenne Muscular Dystrophy During Long-Distance Walking , 2012, Journal of child neurology.
[33] R. Finkel,et al. The Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): Test development and reliability , 2010, Neuromuscular Disorders.
[34] Nathalie Jette,et al. A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy , 2014, Neuromuscular Disorders.
[35] Ruzena Bajcsy,et al. Development and Application of Stereo Camera-Based Upper Extremity Workspace Evaluation in Patients with Neuromuscular Diseases , 2012, PloS one.
[36] E. Mazzone,et al. A critical review of functional assessment tools for upper limbs in Duchenne muscular dystrophy , 2012, Developmental medicine and child neurology.
[37] M. Brooke,et al. Clinical trial in duchenne dystrophy. I. The design of the protocol , 1981, Muscle & nerve.
[38] Susanne Fuchs-Winkelmann,et al. Objective assessment, repeatability, and agreement of shoulder ROM with a 3D gyroscope , 2013, BMC Musculoskeletal Disorders.
[39] Robert E. Mahony,et al. Attitude estimation on SO[3] based on direct inertial measurements , 2006, Proceedings 2006 IEEE International Conference on Robotics and Automation, 2006. ICRA 2006..
[40] J. Mendell,et al. Reliability and validity of active‐seated: An outcome in dystrophinopathy , 2015, Muscle & nerve.
[41] J. Bourke,et al. Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study , 2011, The Lancet.
[42] F. Horak,et al. Trunk accelerometry reveals postural instability in untreated Parkinson's disease. , 2011, Parkinsonism & related disorders.
[43] J. Vissing,et al. Decreased Variability of the 6-Minute Walk Test by Heart Rate Correction in Patients with Neuromuscular Disease , 2014, PloS one.
[44] V. Mathiowetz,et al. Adult norms for the Box and Block Test of manual dexterity. , 1985, The American journal of occupational therapy : official publication of the American Occupational Therapy Association.
[45] Elizabeth Vroom,et al. Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy , 2013, Developmental medicine and child neurology.
[46] G. V. Ommen,et al. Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophy , 2002, Neuromuscular Disorders.
[47] L. Andersen,et al. Health‐related aspects of objectively measured daily physical activity in children , 2008, Clinical physiology and functional imaging.
[48] J. Thonnard,et al. ABILHAND: a Rasch-built measure of manual ability. , 1998, Archives of physical medicine and rehabilitation.
[49] J. Miller,et al. Outcome reliability in non‐Ambulatory Boys/Men with duchenne muscular dystrophy , 2015, Muscle & nerve.
[50] Henk J Stam,et al. Excellent test-retest and inter-rater reliability for Tardieu Scale measurements with inertial sensors in elbow flexors of stroke patients. , 2011, Gait & posture.
[51] Kamiar Aminian,et al. Continuous monitoring and quantification of multiple parameters of daily physical activity in ambulatory Duchenne muscular dystrophy patients. , 2011, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
[52] M. Main,et al. The Hammersmith functional motor scale for children with spinal muscular atrophy: a scale to test ability and monitor progress in children with limited ambulation. , 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
[53] Fendy Santoso,et al. Indoor location-aware medical systems for smart homecare and telehealth monitoring: state-of-the-art , 2015, Physiological measurement.
[54] H. Stam,et al. Upper limb function in adults with Duchenne muscular dystrophy. , 2011, Journal of rehabilitation medicine.
[55] T. Voit,et al. Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients , 2013, Neuromuscular Disorders.
[56] G. Wahba. A Least Squares Estimate of Satellite Attitude , 1965 .
[57] L. Servais,et al. Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial , 2015, PloS one.
[58] Fabrizio Taffoni,et al. A technological approach to studying motor planning ability in children at high risk for ASD , 2014, 2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.
[59] M G Wardle,et al. Use of the Minnesota Rate of Manipulation Test for Disability Evaluation , 1982, Perceptual and motor skills.
[60] Jay J. Han,et al. The 6‐minute walk test as a new outcome measure in Duchenne muscular dystrophy , 2010, Muscle & nerve.
[61] J. Téllez-Zenteno,et al. Ambulatory EEG: a cost-effective alternative to inpatient video-EEG in adult patients , 2012, Epileptic disorders : international epilepsy journal with videotape.
[62] Don C Des Jarlais,et al. Improving the reporting quality of nonrandomized evaluations of behavioral and public health interventions: the TREND statement. , 2004, American journal of public health.
[63] G.H. Elkaim,et al. Extension of a two-step calibration methodology to include nonorthogonal sensor axes , 2008, IEEE Transactions on Aerospace and Electronic Systems.
[64] M. Rose,et al. Construction and validation of a quality of life questionnaire for neuromuscular disease (INQoL) , 2007, Neurology.
[65] A. Emery,et al. The muscular dystrophies , 2002, The Lancet.
[66] Nicolas Petit,et al. Using magnetic disturbances to improve IMU-based position estimation , 2007, 2007 European Control Conference (ECC).
[67] Francesco Muntoni,et al. Dystrophin and mutations: one gene, several proteins, multiple phenotypes , 2003, The Lancet Neurology.
[68] Sabine Van Huffel,et al. Long-term home monitoring of hypermotor seizures by patient-worn accelerometers , 2013, Epilepsy & Behavior.
[69] Ronald M. Aarts,et al. Time-Frequency Analysis of Accelerometry Data for Detection of Myoclonic Seizures , 2010, IEEE Transactions on Information Technology in Biomedicine.
[70] L. Servais,et al. Upper Limb Evaluation and One-Year Follow Up of Non-Ambulant Patients with Spinal Muscular Atrophy: An Observational Multicenter Trial , 2015, PloS one.