First prenatal diagnosis of acyl‐CoA oxidase deficiency
- 1 May 1990
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (3), 371-374
- https://doi.org/10.1007/bf01799398
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
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- Very long chain fatty acids in amniotic fluid from a fetus affected with Zellweger syndromeEuropean Journal of Pediatrics, 1989
- Prenatal and perinatal diagnosis of peroxisomal disordersJournal of Inherited Metabolic Disease, 1989
- Prenatal diagnosis of Zellweger syndrome by determination of trihydroxycoprostanic acid in amniotic fluidEuropean Journal of Pediatrics, 1988
- A NEW PEROXISOMAL DISORDER WITH ENLARGED PEROXISOMES AND A SPECIFIC DEFICIENCY OF ACYL-COA OXIDASE (PSEUDO NEONATAL ADRENOLEUKODYSTROPHY)1988
- Neonatal adrenoleukodystrophy: New cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromesAmerican Journal of Medical Genetics, 1986
- A fatty acyl-CoA oxidizing system in rat liver peroxisomes; enhancement by clofibrate, a hypolipidemic drug.Proceedings of the National Academy of Sciences, 1976