Interventions for increasing ankle range of motion in patients with neuromuscular disease.
暂无分享,去创建一个
K. North | J. Burns | K. Rose | D. Wheeler
[1] A. Scheinberg,et al. Randomized trial of botulinum toxin to prevent pes cavus progression in pediatric charcot–marie–tooth disease type 1A , 2010, Muscle & nerve.
[2] A. Kornberg,et al. Ascorbic acid for Charcot–Marie–Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trial , 2009, The Lancet Neurology.
[3] M. Ryan,et al. Evolution of foot and ankle manifestations in children with CMT1A , 2009, Muscle & nerve.
[4] A. Redmond,et al. Factors that influence health-related quality of life in Australian adults with Charcot–Marie–Tooth disease , 2008, Neuromuscular Disorders.
[5] C. Lynch,et al. Functional Electrical Stimulation , 2008, IEEE Control Systems.
[6] A. Manzur,et al. Glucocorticoid corticosteroids for Duchenne muscular dystrophy. , 2008, The Cochrane database of systematic reviews.
[8] 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.
[9] Rory O'Sullivan,et al. The characteristics of gait in Charcot-Marie-Tooth disease types I and II. , 2007, Gait & posture.
[10] M. Main,et al. Serial casting of the ankles in Duchenne muscular dystrophy: can it be an alternative to surgery? , 2007, Neuromuscular Disorders.
[11] Francesco Muntoni,et al. Muscle MRI in inherited neuromuscular disorders: Past, present, and future , 2007, Journal of magnetic resonance imaging : JMRI.
[12] G. Guyton. Current Concepts Review: Orthopaedic Aspects of Charcot-Marie-Tooth Disease , 2006, Foot & ankle international.
[13] S. Kilbreath,et al. Do voluntary strength, proprioception, range of motion, or postural sway predict occurrence of lateral ankle sprain? , 2006, British Journal of Sports Medicine.
[14] J. Patrick,et al. The Use of Stock Orthoses to Assist Gait in Neuromuscular Disorders: A Pilot Study , 2006, Prosthetics and orthotics international.
[15] H. Dawes,et al. A pilot randomised controlled trial of a home-based exercise programme aimed at improving endurance and function in adults with neuromuscular disorders , 2006, Journal of Neurology, Neurosurgery & Psychiatry.
[16] O. Combarros,et al. Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles. , 2006, Brain : a journal of neurology.
[17] Malcolm Kohler,et al. Quality of life, physical disability, and respiratory impairment in Duchenne muscular dystrophy. , 2005, American journal of respiratory and critical care medicine.
[18] Robert D Herbert,et al. Passive stretching does not enhance outcomes in patients with plantarflexion contracture after cast immobilization for ankle fracture: a randomized controlled trial. , 2005, Archives of physical medicine and rehabilitation.
[19] T. Yan,et al. Functional Electrical Stimulation Improves Motor Recovery of the Lower Extremity and Walking Ability of Subjects With First Acute Stroke: A Randomized Placebo-Controlled Trial , 2005, Stroke.
[20] R. Griggs,et al. Report on the 124th ENMC International Workshop. Treatment of Duchenne muscular dystrophy; defining the gold standards of management in the use of corticosteroids 2–4 April 2004, Naarden, The Netherlands , 2004, Neuromuscular Disorders.
[21] R. Whalen,et al. Effect of heat modalities on hamstring length: a comparison of pneumatherm, moist heat pack, and a control. , 2004, The Journal of orthopaedic and sports physical therapy.
[22] D. Altman,et al. Measuring inconsistency in meta-analyses , 2003, BMJ : British Medical Journal.
[23] M. Eagle. Report on the Muscular Dystrophy Campaign workshop: Exercise in neuromuscular diseases Newcastle, January 2002 , 2002, Neuromuscular Disorders.
[24] S. Mubarak,et al. Surgical Prevention of Foot Deformity in Patients With Duchenne Muscular Dystrophy , 2002, Journal of pediatric orthopedics.
[25] K. Kunze,et al. Disability and quality of life in Charcot-Marie-Tooth disease type 1 , 2001, Journal of neurology, neurosurgery, and psychiatry.
[26] R. Gajdosik,et al. Passive extensibility of skeletal muscle: review of the literature with clinical implications. , 2001, Clinical biomechanics.
[27] M. J. Muêller,et al. Effect of plantar flexor muscle stiffness on selected gait characteristics. , 2000, Gait & posture.
[28] U. Werlauff,et al. A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy , 2000, Neuromuscular Disorders.
[29] N. Latronico. [Nervous system diseases]. , 2000, Minerva pediatrica.
[30] J. Forst,et al. Lower limb surgery in Duchenne muscular dystrophy , 1999, Neuromuscular Disorders.
[31] A. Kroksmark. Physiotherapy in muscular dystrophy. , 1998, Scandinavian journal of rehabilitation medicine. Supplement.
[32] B. Cusick. Serial Casts: Their Use in the Management of Spasticity Induced Foot Deformity , 1998 .
[33] C. McDonald,et al. Limb contractures in progressive neuromuscular disease and the role of stretching, orthotics, and surgery. , 1998, Physical medicine and rehabilitation clinics of North America.
[34] B. Katirji,et al. Evaluation of a Program for Long-Term Treatment of Duchenne Muscular Dystrophy. Experience at the University Hospitals of Cleveland* , 1996, The Journal of bone and joint surgery. American volume.
[35] William M. Fowler,et al. Duchenne muscular dystrophy , 1995 .
[36] S. Siegler,et al. Quantitative identification of ankle equinus with applications for treatment assessment , 1995 .
[37] G. Fenichel,et al. Prolongation of Ambulation in Children with Duchenne Muscular Dystrophy by Subcutaneous Lower Limb Tenotomy , 1993, Journal of pediatric orthopedics.
[38] G. Bentley,et al. A randomized controlled trial of early surgery in duchenne muscular dystrophy , 1992, Neuromuscular Disorders.
[39] A. Emery. Population frequencies of inherited neuromuscular diseases—A world survey , 1991, Neuromuscular Disorders.
[40] V. Dubowitz. Prednisone in Duchenne dystrophy , 1991, Neuromuscular Disorders.
[41] A. Pestronk,et al. Long‐term benefit from prednisone therapy in Duchenne muscular dystrophy , 1991, Neurology.
[42] A. Pestronk,et al. A comparison of daily and alternate-day prednisone therapy in the treatment of Duchenne muscular dystrophy. , 1991, Archives of neurology.
[43] A. Pestronk,et al. Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy Group. , 1991, Archives of neurology.
[44] G. Vrbóva,et al. Therapeutic possibilities of chronic low frequency electrical stimulation in children with Duchenne muscular dystrophy , 1990, Journal of the Neurological Sciences.
[45] J. Miller,et al. Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy. , 1989, The New England journal of medicine.
[46] Michael A. Hutson,et al. Orthopaedic Physical Assessment , 1987 .
[47] G. Vrbóva,et al. Responses of muscles of patients with Duchenne muscular dystrophy to chronic electrical stimulation. , 1986, Journal of neurology, neurosurgery, and psychiatry.
[48] Seeger Br,et al. Progression of equinus deformity in Duchenne muscular dystrophy. , 1985 .
[49] Paul J. Vignos,et al. Physical models of rehabilitation in neuromuscular disease , 1983, Muscle & nerve.
[50] J. Miller,et al. Clinical investigation in duchenne dystrophy: 2. Determination of the “power” of therapeutic trials based on the natural history , 1983, Muscle & nerve.
[51] V. Dubowitz,et al. Prolongation of ambulation in Duchenne muscular dystrophy by appropriate orthoses. , 1982, Physiotherapy.
[52] V. Dubowitz,et al. Prevention of deformity in Duchenne muscular dystrophy. A prospective study of passive stretching and splintage. , 1981, Physiotherapy.
[53] V. Dubowitz,et al. Effect of exercise in Duchenne muscular dystrophy. , 1981, Physiotherapy.
[54] I. Siegel. A clinical review , 1978 .
[55] Siegel Im. Equinocavovarus in muscular dystrophy: treatment by percutaneous tarsal medullostomy and soft tissue release. , 1977 .
[56] C. Reich. Double-blind studies. , 1972, Canadian Medical Association journal.
[57] P. Vignos,et al. Management of progressive muscular dystrophy in childhood. , 1963, JAMA.
[58] Roger E. Kirk,et al. Simple Random Sample , 2011, International Encyclopedia of Statistical Science.
[59] K. Refshauge,et al. Serial night casting increases ankle dorsiflexion range in children and young adults with Charcot-Marie-Tooth disease: a randomised trial. , 2010, Journal of physiotherapy.
[60] K. Refshauge,et al. Night splinting does not increase ankle range of motion in people with Charcot-Marie-Tooth disease: a randomised, cross-over trial. , 2006, The Australian journal of physiotherapy.
[61] Jack Crosbie,et al. Development and validation of a novel rating system for scoring standing foot posture: the Foot Posture Index. , 2006, Clinical biomechanics.
[62] L. Harvey,et al. Does 12 weeks of regular standing prevent loss of ankle mobility and bone mineral density in people with recent spinal cord injuries? , 2005, The Australian journal of physiotherapy.
[63] J. Forst,et al. Importance of lower limb surgery in Duchenne muscular dystrophy , 2004, Archives of Orthopaedic and Trauma Surgery.
[64] E. Sobel,et al. Problems and management of the rearfoot in neuromuscular disease. A report of ten cases. , 1999, Journal of the American Podiatric Medical Association.
[65] R Adams,et al. Measurement of passive ankle dorsiflexion: Procedure and reliability. , 1991, The Australian journal of physiotherapy.
[66] I. Siegel. Prolongation of ambulation through early percutaneous tenotomy and bracing with plastic orthoses. , 1977, Israel journal of medical sciences.
[67] Siegel Im. Orthopedic correction of musculoskeletal deformity in muscular dystrophy. , 1977 .