1. Medium-chain acylCoA dehydrogenase (M-CAD) deficiency in children with non-ketotic hypoglycemia and low carnitine levels;Stanley, C.A.; Hale, D.E.; Coates, P.M.;Pediatr Res,1983
2. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency;Stanley, C.A.;Adv Pediatr,1987
3. Acyl-coA dehydrogenase deficiencies;Roe, C.R.; Coates, P.M.,1989
4. Suberylglycine excretion in the urine from a patient with dicarboxylic acidura;Gregersen, N.; Lauritzen, R.; Rasmussen, K.;Clin Chim Acta,1976
5. Non-ketotic C6-C10 dicarboxylic aciduria: biochemical investigation of two cases;Gregersen, N.; Rosleff, F.; Kolvraa, S.; Hobolth, N.; Rasmussen, K.; Lauritzen, R.;Clin Chim Acta,1980