Responsiveness of gait analysis parameters in a cohort of 71 CMT subjects
暂无分享,去创建一个
Maurizio Ferrarin | Davide Pareyson | Isabella Moroni | Emanuela Pagliano | Gabriele Bovi | Marco Rabuffetti | Luca Padua | Enrica Di Sipio | Tiziana Lencioni | Angelo Schenone | M. Ferrarin | M. Rabuffetti | L. Padua | D. Pareyson | A. Schenone | T. Lencioni | M. Diverio | E. D. Sipio | G. Bovi | E. Pagliano | I. Moroni | Giuseppe Piscosquito | Manuela Diverio | G. Piscosquito
[1] M P Kadaba,et al. Measurement of lower extremity kinematics during level walking , 1990, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[2] Maurizio Ferrarin,et al. Changes of gait pattern in children with Charcot-Marie-Tooth disease type 1A: a 18 months follow-up study , 2013, Journal of NeuroEngineering and Rehabilitation.
[3] Rory O'Sullivan,et al. The characteristics of gait in Charcot-Marie-Tooth disease types I and II. , 2007, Gait & posture.
[4] D. Pareyson,et al. Psychometrics evaluation of Charcot‐Marie‐Tooth Neuropathy Score (CMTNSv2) second version, using Rasch analysis , 2014, Journal of the peripheral nervous system : JPNS.
[5] Jacob Cohen. Statistical Power Analysis for the Behavioral Sciences , 1969, The SAGE Encyclopedia of Research Design.
[6] M Rabuffetti,et al. Gait pattern classification in children with Charcot-Marie-Tooth disease type 1A. , 2012, Gait & posture.
[7] J. McGinley,et al. Gait in children and adolescents with Charcot‐Marie‐Tooth disease: a systematic review , 2016, Journal of the peripheral nervous system : JPNS.
[8] Jun Yu Li,et al. Reliability and validity of the CMT neuropathy score as a measure of disability , 2005, Neurology.
[9] C. McDonald,et al. Clinical approach to the diagnostic evaluation of hereditary and acquired neuromuscular diseases. , 2012, Physical medicine and rehabilitation clinics of North America.
[10] R. Riener,et al. Stair ascent and descent at different inclinations. , 2002, Gait & posture.
[11] V. Scaioli,et al. Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease , 2007, NeuroMolecular Medicine.
[12] M. Mcdermott,et al. Reliability of the CMT neuropathy score (second version) in Charcot‐Marie‐Tooth disease , 2011, Journal of the peripheral nervous system : JPNS.
[13] D. Cornblath,et al. Does ability to walk reflect general functionality in inflammatory neuropathies? , 2016, Journal of the peripheral nervous system : JPNS.
[14] R. D. de Haan,et al. The natural history of Charcot-Marie-Tooth type 1A in adults: a 5-year follow-up study. , 2009, Brain : a journal of neurology.
[15] O. Combarros,et al. The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type I , 1989, Muscle & nerve.
[16] F. Muntoni,et al. 168th ENMC International Workshop: Outcome measures and clinical trials in Charcot–Marie–Tooth disease (CMT) , 2010, Neuromuscular Disorders.
[17] Mariano Serrao,et al. Foot drop and plantar flexion failure determine different gait strategies in Charcot-Marie-Tooth patients. , 2007, Clinical biomechanics.
[18] M. Shy,et al. Charcot‐marie‐tooth disease subtypes and genetic testing strategies , 2011, Annals of neurology.
[19] M. Mcdermott,et al. Neuropathy progression in Charcot-Marie-Tooth disease type 1A , 2008, Neurology.
[20] M. Ferrarin,et al. Reliability of instrumented movement analysis as outcome measure in Charcot–Marie–Tooth disease: Results from a multitask locomotor protocol , 2011, Gait & posture.
[21] L. Padua,et al. Efficacy of focal mechanic vibration treatment on balance in Charcot-Marie-Tooth 1A disease: a pilot study , 2016, Journal of Neurology.
[22] D. Pareyson,et al. Ascorbic acid for the treatment of Charcot-Marie-Tooth disease. , 2015, The Cochrane database of systematic reviews.
[23] Davide Pareyson,et al. Diagnosis, natural history, and management of Charcot–Marie–Tooth disease , 2009, The Lancet Neurology.
[24] M. Shy,et al. Determinants of reduced health-related quality of life in pediatric inherited neuropathies , 2010, Neurology.
[25] A. Thompson,et al. Effect sizes can be misleading: is it time to change the way we measure change? , 2010, Journal of Neurology, Neurosurgery & Psychiatry.
[26] O. Blin,et al. Effect of ascorbic acid in patients with Charcot–Marie–Tooth disease type 1A: a multicentre, randomised, double-blind, placebo-controlled trial , 2009, The Lancet Neurology.
[27] D. Herrmann,et al. Quality-of-life in Charcot–Marie–Tooth disease: The patient’s perspective , 2014, Neuromuscular Disorders.
[28] D. Gladman,et al. Methods for assessing responsiveness: a critical review and recommendations. , 2000, Journal of clinical epidemiology.
[29] C. Fornusek,et al. Relationship between physical performance and quality of life in Charcot‐Marie‐Tooth disease: a pilot study , 2016, Journal of the peripheral nervous system : JPNS.
[30] T. Yousry,et al. MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study , 2016, The Lancet Neurology.
[31] T. Beißbarth,et al. Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients , 2014, Neuromuscular Disorders.
[32] D. Radice,et al. Responsiveness of clinical outcome measures in Charcot−Marie−Tooth disease , 2015, European journal of neurology.
[33] R. Lewis,et al. High-dosage ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A: results of a randomized, double-masked, controlled trial. , 2013, JAMA neurology.
[34] H. Houlden,et al. Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing , 2012, Journal of Neurology, Neurosurgery & Psychiatry.
[35] D. Radice,et al. Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial , 2011, The Lancet Neurology.
[36] M. Ferrarin,et al. Postural stabilization and balance assessment in Charcot–Marie–Tooth 1A subjects , 2014, Gait & posture.
[37] Gyula Acsadi,et al. A comprehensive evaluation of the variation in ankle function during gait in children and youth with Charcot-Marie-Tooth disease. , 2013, Gait & posture.
[38] M. Ferrarin,et al. The influence of somatosensory and muscular deficits on postural stabilization: Insights from an instrumented analysis of subjects affected by different types of Charcot–Marie–Tooth disease , 2015, Neuromuscular Disorders.