31P-nuclear magnetic resonance spectroscopy was used to investigate in vivo the energy metabolism of the calf muscle in a 10-year-old patient with adenylosuccinate lyase deficiency and severe psychomotor retardation. The patient showed a markedly reduced PCr/P(i) molar ratio, known to well represent the cytosolic phosphorylation potential, due to low PCr and high P(i) content in resting muscle. Moreover, intracellular ATP concentration was significantly lower than in the control group both at rest and at the end of post-exercise recovery. The rate of patient's PCr recovery after an exercise in ischaemic conditions was also out of the reference range, suggesting a reduced ability of mitochondria to respond to metabolic needs
The pattern of cytosolic ADP recovery after exercise has not been fully characterized in human skele...
Debranching enzyme deficiency (Glycogen storage disease (GSD) type III) causes progressive muscle wa...
Genetic therapy has changed the prognosis of hereditary proximal spinal muscular atrophy, although t...
Abstract31P-nuclear magnetic resonance spectroscopy was used to investigate in vivo the energy metab...
The muscle energy metabolism in a patient with inherited adenylosuccinate lyase deficiency has been ...
1991-1994, 1985.-In muscle phosphorylase deficiency (Mc-Ardle’s disease) there is an abnormally rapi...
Impairment of muscle glycogenolysis in McArdle's disease (myophosphorylase deficiency) leads to exer...
BACKGROUND: Patients with respiratory failure have early fatiguability which may be due to limitatio...
Objective - To distinguish between the effects of reduced oxidative capacity and reduced metabolic e...
AbstractObjective: Decreased oxygen supply is generally accepted as the primary cause of muscle dysf...
AbstractBioenergetic sufficiency can be quantitatively assayed by nuclear magnetic resonance spectro...
National audienceAbstract: Phosphorus nuclear magnetic resonance spectroscopy enables the energy met...
In this study we assessed ΔG'(ATP) hydrolysis, cytosolic [ADP], and the rate of phosphocreatine reco...
Twenty-four patients with exercise intolerance of undetermined origin were examined by muscle phosph...
P31 NMR spectroscopy is useful for the diagnosis of some myopathies and it is necessary to further s...
The pattern of cytosolic ADP recovery after exercise has not been fully characterized in human skele...
Debranching enzyme deficiency (Glycogen storage disease (GSD) type III) causes progressive muscle wa...
Genetic therapy has changed the prognosis of hereditary proximal spinal muscular atrophy, although t...
Abstract31P-nuclear magnetic resonance spectroscopy was used to investigate in vivo the energy metab...
The muscle energy metabolism in a patient with inherited adenylosuccinate lyase deficiency has been ...
1991-1994, 1985.-In muscle phosphorylase deficiency (Mc-Ardle’s disease) there is an abnormally rapi...
Impairment of muscle glycogenolysis in McArdle's disease (myophosphorylase deficiency) leads to exer...
BACKGROUND: Patients with respiratory failure have early fatiguability which may be due to limitatio...
Objective - To distinguish between the effects of reduced oxidative capacity and reduced metabolic e...
AbstractObjective: Decreased oxygen supply is generally accepted as the primary cause of muscle dysf...
AbstractBioenergetic sufficiency can be quantitatively assayed by nuclear magnetic resonance spectro...
National audienceAbstract: Phosphorus nuclear magnetic resonance spectroscopy enables the energy met...
In this study we assessed ΔG'(ATP) hydrolysis, cytosolic [ADP], and the rate of phosphocreatine reco...
Twenty-four patients with exercise intolerance of undetermined origin were examined by muscle phosph...
P31 NMR spectroscopy is useful for the diagnosis of some myopathies and it is necessary to further s...
The pattern of cytosolic ADP recovery after exercise has not been fully characterized in human skele...
Debranching enzyme deficiency (Glycogen storage disease (GSD) type III) causes progressive muscle wa...
Genetic therapy has changed the prognosis of hereditary proximal spinal muscular atrophy, although t...