Prenatal diagnosis of disorders of fatty acid transport and mitochondrial oxidation
- 31 January 2001
- journal article
- review article
- Published by Wiley in Prenatal Diagnosis
- Vol. 21 (1) , 52-54
- https://doi.org/10.1002/1097-0223(200101)21:1<52::aid-pd973>3.0.co;2-h
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- The HELLP syndrome associated with fetal medium‐chain acyl‐CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 2000
- Inborn Errors of Mitochondrial Fatty Acid OxidationCritical Reviews in Clinical Laboratory Sciences, 2000
- Carnitine Palmitoyltransferase DeficienciesMolecular Genetics and Metabolism, 1999
- Recent Developments in the Investigation of Inherited Metabolic Disorders Using Cultured Human CellsMolecular Genetics and Metabolism, 1999
- A Fetal Fatty-Acid Oxidation Disorder as a Cause of Liver Disease in Pregnant WomenNew England Journal of Medicine, 1999
- DNA-based prenatal diagnosis for very-long- chain acyl-CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1999
- Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal deathThe Journal of Pediatrics, 1997
- Sudden neonatal death in carnitine transporter deficiencyThe Journal of Pediatrics, 1997
- PRENATAL DIAGNOSIS OF MITOCHONDRIAL FATTY ACID OXIDATION DEFECTSPrenatal Diagnosis, 1996
- Prenatal diagnosis of medium‐chain acyl‐coenzyme A dehydrogenase deficiencyPrenatal Diagnosis, 1987