Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency
Mary Anne D. Chiong(University of the Philippines Manila), John Christodoulou(The University of Melbourne), William J. Rhead(Children's Hospital of Wisconsin), Keow Giak Sim(Children's Hospital at Westmead), Kevin Carpenter(The University of Sydney), Rikke Katrine Jentoft Olsen(Aarhus University Hospital), Gladys Ho(The University of Sydney)
Cited by 49
Related Papers
Survival after Treatment with Phenylacetate and Benzoate for Urea-Cycle Disorders
|New England Journal of Medicine|2007|357
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
|Proceedings of the National Academy of Sciences|1998|254
‘Classical’ organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: Long‐term outcome and effects of expanded newborn screening using tandem mass spectrometry
|Journal of Inherited Metabolic Disease|2006|247
Australian children living with rare diseases: experiences of diagnosis and perceived consequences of diagnostic delays
|Orphanet Journal of Rare Diseases|2017|232
Phenylketonuria in adulthood: A collaborative study
|Journal of Inherited Metabolic Disease|2002|215