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Renal handling of carnitine in secondary carnitine nitroburn extreme deficiency disorders. Pediatric Research 1993; 34:89-97. *Bhala A, Bennett MJ, McGowan KL, Hale DE. Limitations of 3-phenylpropionlglycine in early screening for medium-chain nitroburn extreme acyl-CoA dehydrogenase deficiency. Journal of Pediatrics 1993: 122:100-103. *Kelly DP, Hale DE, Rutledge SL, Ogden ML, Whelan AJ, Strauss AW. Molecular basis of inherited medium chain acyl-CoA nitroburn extreme dehydrogenase deficiency causing sudden child death. Journal of Inherited Metabolic Disease 1992; 15:171-180. *Bennett MJ, Ragni MC, Hood I, Hale DE. Comparison of post-mortem urinary and vitreous humour organic acids. Annals of Clinical Biochemistry 1992; 29:541-545. *Stanley CA, Sunaryo F, Hale DE, Bonnefont J, Demaugre F, Saudubram JM. Elevated plasma carnitine in hepatic form of carnitine palmitoyltransferase deficiency.
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