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THE 6-minute walk test and other endpoints in Duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study

Muscle & nerve, 2013-09, Vol.48 (3), p.343-356

2013

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The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: Reliability, concurrent validity, and minimal clinically important differences from a multicenter study

Muscle & nerve, 2013-09, Vol.48 (3), p.357-368

2013

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The 6-minute walk test as a new outcome measure in Duchenne muscular dystrophy

Muscle & nerve, 2010-04, Vol.41 (4), p.500-510

2010

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Use of step activity monitoring for continuous physical activity assessment in boys with Duchenne muscular dystrophy

Archives of physical medicine and rehabilitation, 2005-04, Vol.86 (4), p.802-808

2005

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Utility of a step activity monitor for the measurement of daily ambulatory activity in children

Archives of physical medicine and rehabilitation, 2005-04, Vol.86 (4), p.793-801

2005

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Exercise in neuromuscular diseases

Physical medicine and rehabilitation clinics of North America, 2012-08, Vol.23 (3), p.653

2012

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(−)‐Epicatechin induces mitochondrial biogenesis and markers of muscle regeneration in adults with Becker muscular dystrophy

Muscle & nerve, 2021-02, Vol.63 (2), p.239-249

2021

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The cooperative international neuromuscular research group Duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures

Muscle & nerve, 2013-07, Vol.48 (1), p.55-67

2013

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The cooperative international neuromuscular research group duchenne natural history study-a longitudinal investigation in the era of glucocorticoid therapy: Design of protocol and the methods used

Muscle & nerve, 2013-07, Vol.48 (1), p.32-54

2013

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Pulmonary Endpoints in Duchenne Muscular Dystrophy. A Workshop Summary

American journal of respiratory and critical care medicine, 2017-08, Vol.196 (4), p.512-519

2017

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Rehabilitation management of neuromuscular disease: the role of exercise training

Journal of clinical neuromuscular disease, 2009-09, Vol.11 (1), p.7

2009

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Physical therapy evaluation and management in neuromuscular diseases

Physical medicine and rehabilitation clinics of North America, 2012-08, Vol.23 (3), p.633

2012

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The 6-minute walk test in Duchenne/Becker muscular dystrophy: Longitudinal observations

Muscle & nerve, 2010-12, Vol.42 (6), p.966-974

2010

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Quality-of-Life Measures in Children With Neurological Conditions: Pediatric Neuro-QOL

Neurorehabilitation and neural repair, 2012-01, Vol.26 (1), p.36-47

2012

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Validity, Reliability, and Sensitivity of a 3D Vision Sensor-based Upper Extremity Reachable Workspace Evaluation in Neuromuscular Diseases

PLoS currents, 2013-12, Vol.5

2013

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Validity and reliability of smartphone magnetometer-based goniometer evaluation of shoulder abduction – A pilot study

Manual therapy, 2015-12, Vol.20 (6), p.777-782

2015

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Electromyographic studies in mdx and wild-type C57 mice

Muscle & nerve, 2006-02, Vol.33 (2), p.208-214

2006

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Effectiveness of an Upper Extremity Exercise Device Integrated With Computer Gaming for Aerobic Training in Adolescents With Spinal Cord Dysfunction

The journal of spinal cord medicine, 2006-01, Vol.29 (4), p.363-370

2006

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Disease burden in neuromuscular disease: the role of chronic pain

Physical medicine and rehabilitation clinics of North America, 2012-08, Vol.23 (3), p.719

2012

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Respiratory abdominal muscle recruitment and chest wall motion in myotonic muscular dystrophy

Journal of applied physiology (1985), 2001-07, Vol.91 (1), p.395-407

2001

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mHealth application for upper extremity range of motion and reachable workspace

Studies in health technology and informatics, 2013, Vol.184, p.478

2013

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Modafinil to treat fatigue in amyotrophic lateral sclerosis: An open label pilot study

American journal of hospice & palliative medicine, 2005-01, Vol.22 (1), p.55-59

2005

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Altered body composition affects resting energy expenditure and interpretation of body mass index in children with spinal cord injury

The journal of spinal cord medicine, 2004, Vol.27 Suppl 1, p.S24-S28

2004

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The Importance of Assessing Quality of Life in Patients with Neuromuscular Disorders

American journal of hospice & palliative medicine, 2007-12, Vol.23 (6), p.493-497

2007

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LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy

Annals of neurology, 2013-04, Vol.73 (4), p.481-488

2013

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THE 6-minute walk test and other endpoints in Duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study

The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: Reliability, concurrent validity, and minimal clinically important differences from a multicenter study

The 6-minute walk test as a new outcome measure in Duchenne muscular dystrophy

Use of step activity monitoring for continuous physical activity assessment in boys with Duchenne muscular dystrophy

Utility of a step activity monitor for the measurement of daily ambulatory activity in children

Exercise in neuromuscular diseases

(−)‐Epicatechin induces mitochondrial biogenesis and markers of muscle regeneration in adults with Becker muscular dystrophy

The cooperative international neuromuscular research group duchenne natural history study-a longitudinal investigation in the era of glucocorticoid therapy: Design of protocol and the methods used

Pulmonary Endpoints in Duchenne Muscular Dystrophy. A Workshop Summary

Rehabilitation management of neuromuscular disease: the role of exercise training

Physical therapy evaluation and management in neuromuscular diseases

The 6-minute walk test in Duchenne/Becker muscular dystrophy: Longitudinal observations

Quality-of-Life Measures in Children With Neurological Conditions: Pediatric Neuro-QOL

Validity, Reliability, and Sensitivity of a 3D Vision Sensor-based Upper Extremity Reachable Workspace Evaluation in Neuromuscular Diseases

Validity and reliability of smartphone magnetometer-based goniometer evaluation of shoulder abduction – A pilot study

Electromyographic studies in mdx and wild-type C57 mice

Effectiveness of an Upper Extremity Exercise Device Integrated With Computer Gaming for Aerobic Training in Adolescents With Spinal Cord Dysfunction

Disease burden in neuromuscular disease: the role of chronic pain

Respiratory abdominal muscle recruitment and chest wall motion in myotonic muscular dystrophy

mHealth application for upper extremity range of motion and reachable workspace

Modafinil to treat fatigue in amyotrophic lateral sclerosis: An open label pilot study

Altered body composition affects resting energy expenditure and interpretation of body mass index in children with spinal cord injury

The Importance of Assessing Quality of Life in Patients with Neuromuscular Disorders

LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy

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