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5 in total

1. Acquired deficiency of long-chain acyl-CoA dehydrogenase in liver: a cautionary tale.

Authors: F Allison; M J Bennett; R J Pollitt; S Variend
Journal: J Inherit Metab Dis Date: 1990 Impact factor: 4.982

2. Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients.

Authors: T Aoyama; M Souri; S Ushikubo; T Kamijo; S Yamaguchi; R I Kelley; W J Rhead; K Uetake; K Tanaka; T Hashimoto
Journal: J Clin Invest Date: 1995-06 Impact factor: 14.808

3. Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.

Authors: I Tein; D C De Vivo; D Ranucci; S DiMauro
Journal: J Inherit Metab Dis Date: 1993 Impact factor: 4.982

4. Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.

Authors: M J Bennett; R J Pollitt; S I Goodman; D E Hale; J Vamecq
Journal: J Inherit Metab Dis Date: 1991 Impact factor: 4.982

Review 5. New developments in the diagnosis and investigation of mitochondrial fatty acid oxidation disorders.

Authors: P M Coates
Journal: Eur J Pediatr Date: 1994 Impact factor: 3.183

5 in total