Results
1 -
6 of
6Generalised Dicarboxylic Aciduria: A Common Finding in Neonates, Journal of Inherited Metabolic Disease Organic acids in aqueous humour and plasma: Post mortem study in infants and diagnosis of enzymopathies, Journal of Inherited Metabolic Disease 3-Hydroxydicarboxylic aciduria: A distinctive type of intermittent dicarboxylic aciduria of possible diagnostic significance, Journal of Inherited Metabolic Disease Generalised Dicarboxylic Aciduria: A Common Finding in Neonates, Studies in Inherited Metabolic Disease Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment, European Journal of Pediatrics