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Detection of Spinal Muscular Atrophy Carriers in a Sample of the Brazilian Population
(Karger, 2011-01-01)
Background: Spinal muscular atrophy is a common autosomal recessive neuromuscular disorder caused by mutations in the SMN1 gene. Identification of spinal muscular atrophy carriers has important implications for individuals ...
Exercise training prevents hyperinsulinemia, muscular glycogen loss and muscle atrophy induced by dexamethasone treatment
(Springer, 2010-03-01)
This study investigated whether exercise training could prevent the negative side effects of dexamethasone. Rats underwent a training period and were either submitted to a running protocol (60% physical capacity, 5 days/week ...
Exercise training prevents hyperinsulinemia, muscular glycogen loss and muscle atrophy induced by dexamethasone treatment
(Springer, 2010-03-01)
This study investigated whether exercise training could prevent the negative side effects of dexamethasone. Rats underwent a training period and were either submitted to a running protocol (60% physical capacity, 5 days/week ...
Neuronal involvement in muscular atrophy
(FRONTIERS RESEARCH FOUNDATION, 2014)
Number of muscular fibers by microscopic field: A simple and efficient method to study denervation
(1989-12-01)
An experimental research was performed in dogs to evaluate the changes in gracilis muscle fibers when this muscle is submitted to denervation sectioning its motor nerve. Two experimental groups of six dogs each were used. ...
Combined therapies for Duchenne muscular dystrophy to optimize treatment efficacy
(Frontiers Media, 2018-04)
Duchene Muscular Dystrophy (DMD) is the most frequent muscular dystrophy and one of the most severe due to the absence of the dystrophin protein. Typical pathological features include muscle weakness, muscle wasting, ...