Regional variation in brain lactate in leigh syndrome by localized1H magnetic resonance spectroscopy
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference15 articles.
1. Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: Clues to pathogenesis of Leigh disease
2. Cytochromec oxidase deficiency in leigh syndrome
3. Complex I (reduced nicotinamide-adenine dinucleotide-coenzyme Q reductase) deficiency in two patients with probable Leigh syndrome
4. Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia
5. Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver
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