Browsing by Subject "Duchenne muscular dystrophy"
Now showing items 1-10 of 14
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Achievement of Virtual and Real Objects Using a Short-Term Motor Learning Protocol in People with Duchenne Muscular Dystrophy: A Crossover Randomized Controlled Trial
(Mary Ann Liebert, Inc, 2018)Objective: To evaluate whether people with Duchenne muscular dystrophy (DMD) practicing a task in a virtual environment could improve performance given a similar task in a real environment, as well as distinguishing whether ...
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Boys With Duchenne Muscular Dystrophy: 1-Year Locomotor Changes in Relation to a Control Group
(Sage Publications Inc, 2018)We compared the timed performance and compensatory movements of 32 boys (mean age = 10.0 years) with Duchenne muscular dystrophy (DMD) and 38 healthy boys (mean age = 9.2 years) on 10-meter walking and four-step stair work ...
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Caracterização da modulação autonômica e do perfil funcional de pessoas com Distrofia Muscular de Duchenne
(Universidade Federal de São Paulo (UNIFESP), 2016-10-17)Among Muscular Dystrophies, Duchenne muscular dystrophy (DMD) is the most common genetic neuromuscular disease. Abnormal autonomic signaling is increasingly recognized as an important symptom in neuromuscular diseases, ...
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Computer task performance by subjects with Duchenne muscular dystrophy
(Dove Medical Press Ltd, 2016)Aims: Two specific objectives were established to quantify computer task performance among people with Duchenne muscular dystrophy (DMD). First, we compared simple computational task performance between subjects with DMD ...
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Computer task performance by subjects with Duchenne muscular dystrophy
(Dove Medical Press Ltd, 2016)Aims: Two specific objectives were established to quantify computer task performance among people with Duchenne muscular dystrophy (DMD). First, we compared simple computational task performance between subjects with DMD ...
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Cyclooxygenase-2 expression in skeletal muscle of knockout mice suffering Duchenne muscular dystrophy
(Springer, 2013-05-01)The purpose of the present study was to investigate the role of cyclooxygenase-2 (COX-2) expression in fibrotic lesion in mdx mice. A total of six male C57BL/10 mice and six C57BL/10-DMD/mdx were distributed into two groups: ...
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Duchenne muscular dystrophy: alpha-dystroglycan immunoexpression in skeletal muscle and cognitive performance
(Academia Brasileira de Neurologia - ABNEURO, 2005-12-01)The Duchenne muscular systrophy (DMD) is a muscular dystrophy with cognitive impairment present in 20-30% of the cases. In the present study, in order to study the relationship between the alpha-dystroglycan (alpha-DG) ...
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Heart Rate Variability and Cardiopulmonary Dysfunction in Patients with Duchenne Muscular Dystrophy: A Systematic Review
(Springer, 2018)Duchenne muscular dystrophy (DMD) is a genetic recessive disorder with progressive muscle weakness. Despite the general muscle wasting, degeneration and necrosis of cardiomyocytes have been the main causes of morbidity and ...
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Impact of corticotherapy, nutrition, and sleep disorder on quality of life of patients with Duchenne muscular dystrophy
(Elsevier Science Inc, 2016)Duchenne muscular dystrophy (DMD) is the second most common hereditary genetic disease in humans and has elevated mortality. DMD is an X-linked, life-limiting progressive muscle-wasting disease found predominantly in boys ...
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Patients with Duchenne and Becker muscular dystrophies are not more asymmetrical than healthy controls on timed performance of upper limb tasks
(Assoc Bras Divulg Cientifica, 2017)This study aimed to investigate possible asymmetries and relationships between performance of dominant and non-dominant upper limbs (UL) in patients with Duchenne and Becker muscular dystrophies (DMD/BMD), to compare UL ...