We studied the physiologic adaptation of patients with mitochondrial myopathies to aerobic training. Ten patients underwent individually supervised, moderate-intensity aerobic training on a treadmill for 8 weeks. Biochemical and functional measures improved with training. Estimated aerobic capacity increased by 30%. Blood lactate concentrations at rest and after exercise decreased by 30%. Muscle phosphorus magnetic resonance spectroscopy measurements of adenosine diphosphate recovery after exercise improved by more than 60%. Fatigue and tolerance to daily activities also improved. Although the improvement in exercise tolerance may be due in part to reversal of the effects of secondary deconditioning, this uncontrolled clinical trial suggest...
Exercise and exercise training induces several physiological adaptations that increase the oxidative...
Common impairments experienced by patients with myopathy include muscle weakness, reduced endurance ...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
We studied the physiologic adaptation of patients with mitochondrial myopathies to aerobic training....
We have previously demonstrated that patients with mitochondrial myopathies can benefit from short-t...
Exercise therapy improves mitochondrial function in patients with mitochondrial myopathy (MM). We un...
In mitochondrial myopathies with respiratory chain deficiency impairment of energy cell production m...
Mitochondrial myopathies with respiratory chain defects are multisystem diseases characte-rised by m...
Aerobic training can be effective in patients with mitochondrial myopathies (MM) and McArdle's disea...
There is no generally effective therapy for mitochondrial myopathies. In this study, we measured res...
Patients with mitochondrial myopathies characteristically exhibit pronounced exercise intolerance, o...
Patients with mitochondrial myopathy (MM) have a reduced capacity to perform exercise due to a reduc...
Mitochondrial myopathies are a heterogeneous group of disorders characterized by genetically determi...
Fatigue and exercise intolerance are symptoms in children with metabolic myopathy. Frequently this i...
Impaired skeletal muscle oxidative phosphorylation in patients with severe mitochondrial respiratory...
Exercise and exercise training induces several physiological adaptations that increase the oxidative...
Common impairments experienced by patients with myopathy include muscle weakness, reduced endurance ...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
We studied the physiologic adaptation of patients with mitochondrial myopathies to aerobic training....
We have previously demonstrated that patients with mitochondrial myopathies can benefit from short-t...
Exercise therapy improves mitochondrial function in patients with mitochondrial myopathy (MM). We un...
In mitochondrial myopathies with respiratory chain deficiency impairment of energy cell production m...
Mitochondrial myopathies with respiratory chain defects are multisystem diseases characte-rised by m...
Aerobic training can be effective in patients with mitochondrial myopathies (MM) and McArdle's disea...
There is no generally effective therapy for mitochondrial myopathies. In this study, we measured res...
Patients with mitochondrial myopathies characteristically exhibit pronounced exercise intolerance, o...
Patients with mitochondrial myopathy (MM) have a reduced capacity to perform exercise due to a reduc...
Mitochondrial myopathies are a heterogeneous group of disorders characterized by genetically determi...
Fatigue and exercise intolerance are symptoms in children with metabolic myopathy. Frequently this i...
Impaired skeletal muscle oxidative phosphorylation in patients with severe mitochondrial respiratory...
Exercise and exercise training induces several physiological adaptations that increase the oxidative...
Common impairments experienced by patients with myopathy include muscle weakness, reduced endurance ...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...