Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life
Open Access
- 1 June 1998
- journal article
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 132 (6), 924-933
- https://doi.org/10.1016/s0022-3476(98)70385-3
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Pathology of Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Caused by the G1528C MutationPediatric Pathology & Laboratory Medicine, 1997
- Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?European Journal of Pediatrics, 1995
- Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysisEuropean Journal of Pediatrics, 1994
- Medium–chain acyl-coenzyme A dehydrogenase deficiency: Clinical course in 120 affected childrenThe Journal of Pediatrics, 1994
- The frequency of a disease‐causing point mutation in the gene coding for medium‐chain acyl‐CoA dehydrogenase in sudden infant death syndromeActa Paediatrica, 1993
- Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndromeThe Journal of Pediatrics, 1993
- Fatty acid oxidation disorders: A new class of metabolic diseasesThe Journal of Pediatrics, 1992
- Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptakeAnnals of Neurology, 1991
- Molecular basis of inherited medium‐chain acyl‐CoA dehydrogenase deficiency causing sudden child deathJournal of Inherited Metabolic Disease, 1991
- Evidence of duration and type of illness in children found unexpectedly dead.Archives of Disease in Childhood, 1976