There is no generally effective therapy for mitochondrial myopathies. In this study, we measured responses to combined aerobic training and oral dichloroacetate (DCA) therapy in a 25-year-old woman with a mitochondrial myopathy caused by cytochrome oxidase deficiency. The patient trained for 14 weeks, and DCA therapy was begun after 8 weeks. Independent indices of aerobic capacity and oxidative metabolism showed substantial improvement. Venous lactate concentrations at rest, and after a constant amount of work, decreased by approximately 50% after 8 weeks of aerobic training, and by more than 70% with the combination of training and DCA treatment. Heart rate at rest and after a constant amount of submaximal work decreased progressively. Aer...
We performed a short-term, double-blind, placebo-controlled, crossover trial of sodium dichloroaceta...
Patients with mitochondrial myopathy (MM) have a reduced capacity to perform exercise due to a reduc...
In the mild subtype of inherited carnitine palmitoyltransferase II (CPTII) deficiency, muscular mito...
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...
We have previously demonstrated that patients with mitochondrial myopathies can benefit from short-t...
We studied the physiologic adaptation of patients with mitochondrial myopathies to aerobic training....
In mitochondrial myopathies with respiratory chain deficiency impairment of energy cell production m...
Aerobic training can be effective in patients with mitochondrial myopathies (MM) and McArdle's disea...
Mitochondrial myopathies with respiratory chain defects are multisystem diseases characte-rised by m...
Exercise therapy improves mitochondrial function in patients with mitochondrial myopathy (MM). We un...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
Background: A high-fat diet has been recommended for the treatment of patients with mitochondrial my...
We performed a short-term, double-blind, placebo-controlled, crossover trial of sodium dichloroaceta...
Patients with mitochondrial myopathy (MM) have a reduced capacity to perform exercise due to a reduc...
In the mild subtype of inherited carnitine palmitoyltransferase II (CPTII) deficiency, muscular mito...
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...
We have previously demonstrated that patients with mitochondrial myopathies can benefit from short-t...
We studied the physiologic adaptation of patients with mitochondrial myopathies to aerobic training....
In mitochondrial myopathies with respiratory chain deficiency impairment of energy cell production m...
Aerobic training can be effective in patients with mitochondrial myopathies (MM) and McArdle's disea...
Mitochondrial myopathies with respiratory chain defects are multisystem diseases characte-rised by m...
Exercise therapy improves mitochondrial function in patients with mitochondrial myopathy (MM). We un...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
Myotonic Dystrophy type 1 (DM1) is a dominantly inherited disease comprehending multiple features. F...
Background: A high-fat diet has been recommended for the treatment of patients with mitochondrial my...
We performed a short-term, double-blind, placebo-controlled, crossover trial of sodium dichloroaceta...
Patients with mitochondrial myopathy (MM) have a reduced capacity to perform exercise due to a reduc...
In the mild subtype of inherited carnitine palmitoyltransferase II (CPTII) deficiency, muscular mito...