Reliability of home-based, motor function measure in hereditary neuromuscular diseases
نویسندگان
چکیده
منابع مشابه
Reliability of home-based, motor function measure in hereditary neuromuscular diseases
Objective To evaluate the reliability of the motor function measure (MFM) scale in the assessment of disease severity and progression when administered at home and clinic and assess its correlation with the Paediatric Outcomes Data Collection Instrument (PODCI). Methods In this prospective study, two assessors rated children with hereditary neuromuscular diseases (HNMDs) using the MFM at the cl...
متن کاملResponsiveness of the motor function measure in neuromuscular diseases.
OBJECTIVES To study the responsiveness (sensitivity to change) of the Motor Function Measure (MFM) in detecting change in neuromuscular disease patients with the intent of using this measure in future clinical trials. DESIGN Prospective cohort observational study. SETTING Inpatient and outpatient facilities for follow-up and treatment of neuromuscular diseases. PARTICIPANTS Patients (N=15...
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OBJECTIVE To validate a useful version of the Motor Function Measure (MFM) in children with neuromuscular diseases aged <7 years old. DESIGN Two prospective cohort studies that documented the MFM completion of children aged between 2 and 7 years old. SETTING French-speaking rehabilitation departments from France, Belgium, and Switzerland. PARTICIPANTS Healthy children (n=194) and children...
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A new scale for motor function measurement has been developed for neuromuscular diseases. The validation study included 303 patients, aged 6–62 years. Seventy-two patients had Duchenne muscular dystrophy, 32 Becker muscular dystrophy, 30 limb-girdle muscular dystrophy, 39 facio-scapulo-humeral dystrophy, 29 myotonic dystrophy, 21 congenital myopathy, 10 congenital muscular dystrophy, 35 spinal ...
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ژورنال
عنوان ژورنال: Journal of International Medical Research
سال: 2017
ISSN: 0300-0605,1473-2300
DOI: 10.1177/0300060516674608