Acta Neurologica Scandinavica · 2009 · 39 citations · 33 references
Life SciencesBiochemistryNeurologyCellular MetabolismEnzymologyMetabolismEnergy MetabolismEnzyme DeficienciesMetabolic DisordersMetabolic Pathway DefectsMitochondrial MetabolismOxidative PhosphorylationLeigh SyndromeOxidationOxidative Phosphorylation DefectsOxidative Phosphorylation DeficiencyOxidative Phosphorylation DysfunctionOxidative Phosphorylation ImpairmentPyruvate MetabolismPyruvate Oxidation
We studied a 17-year-old girl with subacute necrotizing encephalomyelopathy (Leigh syndrome). Lactate and pyruvate levels were increased in serum and cerebrospinal fluid. The oxidation rates of all substrates tested, i.e. pyruvate in liver, and pyruvate, malate and 2-oxoglutarate in muscle, were decreased, as was the production of adenosine triphosphate plus creatine phosphate. Cytochrome content was normal. The data imply a defect in oxidative phosphorylation, outside the cytochrome region.
33
Handbook of Clinical Neurology, vol 4.
Dwight Palmer · Archives of Internal Medicine · 1970 · 1K citations
Health Professions, Neurology, Speech-language Pathology +17
Merton Utter, D.B. Keech · Journal of Biological Chemistry · 1963 · 441 citations · Full text