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5 in total

1. Sudden infant death and inherited disorders of fat oxidation.

Authors:
Journal: Lancet Date: 1986-11-08 Impact factor: 79.321

2. Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.

Authors: P Rinaldo; J J O'Shea; P M Coates; D E Hale; C A Stanley; K Tanaka
Journal: N Engl J Med Date: 1988-11-17 Impact factor: 91.245

3. Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes.

Authors: C R Roe; D S Millington; D A Maltby; P Kinnebrew
Journal: J Pediatr Date: 1986-01 Impact factor: 4.406

4. Application of high resolution fast atom bombardment and constant B/E ratio linked scanning to the identification and analysis of acylcarnitines in metabolic disease.

Authors: D S Millington; C R Roe; D A Maltby
Journal: Biomed Mass Spectrom Date: 1984-05

5. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.

Authors: P M Coates; D E Hale; C A Stanley; B E Corkey; J A Cortner
Journal: Pediatr Res Date: 1985-07 Impact factor: 3.756

5 in total

1 in total

1. Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.

Authors: M J Bennett; P M Coates; D E Hale; D S Millington; R J Pollitt; P Rinaldo; C R Roe; K Tanaka
Journal: J Inherit Metab Dis Date: 1990 Impact factor: 4.982

1 in total