Medium-chain acyl-CoA dehydrogenase deficiency presenting in the neonatal period: The first Italian case
- 1 November 1995
- journal article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 154 (11) , 940-941
- https://doi.org/10.1007/bf01957515
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- The enzymes of mitochondrial fatty acid oxidationClinica Chimica Acta; International Journal of Clinical Chemistry, 1994
- Medium–chain acyl-coenzyme A dehydrogenase deficiency: Clinical course in 120 affected childrenThe Journal of Pediatrics, 1994
- Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiency.Archives of Disease in Childhood, 1993
- Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency: The Prevalent Mutation G985 (K304E) Is Subject to a Strong Founder Effect from Northwestern EuropeHuman Heredity, 1993
- Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: Report of two siblingsEuropean Journal of Pediatrics, 1990