Published in Eur Neurol on October 19, 2013
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Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy. Can J Cardiol (2009) 0.98
Comparison and correlates of participation in older adults without disabilities. Arch Gerontol Geriatr (2009) 0.96
Comparison of peak shoulder and elbow mechanical loads during weight-relief lifts and sitting pivot transfers among manual wheelchair users with spinal cord injury. J Rehabil Res Dev (2008) 0.96
Evaluating the integration of chronic disease prevention and management services into primary health care. BMC Health Serv Res (2013) 0.95
Life-space mobility of middle-aged and older adults at various stages of usage of power mobility devices. Arch Phys Med Rehabil (2010) 0.92
Validity of the Assessment of Life Habits in older adults. J Rehabil Med (2004) 0.92
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Electromyographic patterns of upper extremity muscles during sitting pivot transfers performed by individuals with spinal cord injury. J Electromyogr Kinesiol (2008) 0.91
Biomechanical assessment of sitting pivot transfer tasks using a newly developed instrumented transfer system among long-term wheelchair users. J Biomech (2008) 0.90
Comparison of two functional independence scales with a participation measure in post-stroke rehabilitation. Arch Gerontol Geriatr (2003) 0.90
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Quantification of reaction forces during sitting pivot transfers performed by individuals with spinal cord injury. J Rehabil Med (2008) 0.88
Participation after stroke compared to normal aging. J Rehabil Med (2005) 0.88
Effect of a home leisure education program after stroke: a randomized controlled trial. Arch Phys Med Rehabil (2007) 0.88
Daytime sleepiness and myotonic dystrophy. Curr Neurol Neurosci Rep (2013) 0.87
Validation of the Reintegration to Normal Living Index for community-dwelling persons with chronic spinal cord injury. Arch Phys Med Rehabil (2012) 0.86
Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster. Neuromuscul Disord (2008) 0.86
Social participation of older adults in Quebec. Aging Clin Exp Res (2004) 0.85
Coping strategies and social participation in older adults. Gerontology (2008) 0.85
Towards an integrative approach to the management of myotonic dystrophy type 1. J Neurol Neurosurg Psychiatry (2007) 0.85
The development of the spinal cord injury participation and quality of life (PAR-QoL) tool-kit. Disabil Rehabil (2012) 0.84
Biomechanical analysis of a posterior transfer maneuver on a level surface in individuals with high and low-level spinal cord injuries. Clin Biomech (Bristol, Avon) (2003) 0.84
Prevalence of lifestyle risk factors in myotonic dystrophy type 1. Can J Neurol Sci (2013) 0.83
A review of participation instruments based on the International Classification of Functioning, Disability and Health. Disabil Rehabil (2009) 0.82
Comparing the validity of five participation instruments in persons with spinal conditions. J Rehabil Med (2010) 0.82
Fatigue and daytime sleepiness in patients with myotonic dystrophy type 1: to lump or split? Neuromuscul Disord (2009) 0.81
Comparing the reliability of five participation instruments in persons with spinal conditions. J Rehabil Med (2010) 0.81
C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia. Arch Neurol (2012) 0.81
Domain sets and measurement instruments on participation and environmental factors in spinal cord injury research. Am J Phys Med Rehabil (2011) 0.81
Long-term changes in participation after stroke. Top Stroke Rehabil (2006) 0.80
Community needs of people living with spinal cord injury and their family. Top Spinal Cord Inj Rehabil (2012) 0.80
Life habits in myotonic dystrophy type 1. J Rehabil Med (2007) 0.79
Clinical presentation and early evolution of spastic ataxia of Charlevoix-Saguenay. Mov Disord (2013) 0.79
DOK7 mutations presenting as a proximal myopathy in French Canadians. Neuromuscul Disord (2010) 0.78
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Development and cognitive testing of the Nottwil Environmental Factors Inventory in Canada, Switzerland and the USA. J Rehabil Med (2015) 0.78
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Standardized finger-nose test validity for coordination assessment in an ataxic disorder. Can J Neurol Sci (2004) 0.77
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The potential of disease management for neuromuscular hereditary disorders. Rehabil Nurs (2009) 0.77
Anticipation in myotonic dystrophy type 1 parents with small CTG expansions. Am J Med Genet A (2015) 0.76
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Assessing interprofessional teamwork in a videoconference-based telerehabilitation setting. J Telemed Telecare (2008) 0.76
Intergenerational contraction of the CTG repeats in 2 families with myotonic dystrophy type 1. Neurology (2009) 0.76
Effect of rehabilitation length of stay on outcomes in individuals with traumatic brain injury or spinal cord injury: a systematic review protocol. Syst Rev (2013) 0.75
Role for the central motor system in fibromyalgia: pain resolution after pontine infarction. Joint Bone Spine (2009) 0.75
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Autosomal recessive spastic ataxia of Charlevoix-Saguenay: upper extremity aptitudes, functional independence and social participation. Int J Rehabil Res (2004) 0.75
POEMS Syndrome Complicated by Extensive Calciphylaxis: A Remarkable Recovery. J Cutan Med Surg (2015) 0.75
Adaptation of a seated postural control measure for adult wheelchair users. Disabil Rehabil (2005) 0.75
Lower limb muscle impairment in myotonic dystrophy type 1: the need for better guidelines. Muscle Nerve (2015) 0.75
Strength-Training Induces Skeletal Muscle Adaptations in Patients with Myotonic Dystrophy Type I: A Case Study: 2302 June 2, 3: 45 PM - 4: 00 PM. Med Sci Sports Exerc (2016) 0.75
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Reliability of the seated postural control measure for adult wheelchair users. Disabil Rehabil (2005) 0.75
Stanford Chronic Disease Self-Management Program in myotonic dystrophy: New opportunities for occupational therapists: Stanford Chronic Disease Self-Management Program dans la dystrophie myotonique : De nouvelles opportunités pour les ergothérapeutes. Can J Occup Ther (2016) 0.75
Presence of palmar xanthomas in myotonic dystrophy identifies different patterns of linkage disequilibrium between the apolipoprotein E and myotonic dystrophy protein kinase loci. Genet Med (2005) 0.75
Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population. Eur J Hum Genet (2002) 0.75