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Back to Archived Journals Research and Reports in Neonatology Volume 6 Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives Authors Soler-Alfonso C, Bennett M, Ficicioglu C Received 3 June 2015 Accepted for publication 16 September 2015 Published 18 January 2016 Volume 2016:6 Pages 110 DOI Checked for plagiarism Yes Review by Single anonymous peer review Peer reviewer comments 5 Editor who approved publication: Dr Robert Schelonka Claudia Soler-Alfonso, 1 Michael J Bennett, 2 Can Ficicioglu 1 1 Department of Pediatrics, Section of Metabolic Disease, 2 Department of Pathology and Laboratory Medicine, The Childrens Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA Abstract: Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common disorder associated with fatty acid oxidation

psychotic symptoms of individuals with amphetamine psychosis may be due exclusively to heavy use of the drug or heavy use of the drug may exacerbate an underlying vulnerability to schizophrenia

As seen previously, proteins are the nutrients that burn the most fat

This reprogramming of energy metabolism (the Warburg effect) not only overturns conventional theories of the cellular energy supply but also highlights the central role of metabolic dysregulation in tumorigenesis and progression [5]