Subject
Pediatrics, Perinatology and Child Health
Reference7 articles.
1. Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of non-ketotic hypoglycemia;Hale, D.E.; Batshaw, M.L.; Coates, P.M.;Pediatr Res,1985
2. Riboflavin-responsive ethymalonic-adipic aciduria;Green, A.; Marshall, T.G.; Bennett, M.J.; Grey, R.G.F.; Pollitt, R.J.;J Inher Metab Dis,1985
3. General (mediumchain) acyl-CoA dehydrogenase deficiency (non-ketoic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant metabolites in 3 cases;Gregersen, N.; K0lvraa, S.; Rasmussen, K.;Clin Chim Acta,1983
4. Dicarboxylic aciduria and medium chain triglyceride supplemented milk;Henderson, M.J.; Dear, P.R.F.;Arch Dis Child,1986
5. Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes;Roe, C.R.; Millington, D.S.; Maltby, D.A.; Kinnebrew, P.;J Pediatr,1986
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