References

websites

• Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry
• Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiency.
• Morbidity and mortality in medium chain acyl coenzyme A dehydrogenase deficiency.
• Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis
• Fatty infiltration in the liver in medium chain acyl CoA dehydrogenase deficiency.
• L-Carnitine
• Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.

• Protein misfolding is the molecular mechanism underlying MCADD identified in newborn screening
• The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?

• A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causesmild MCAD deficiency: a case report
  

• Medium chain acyl-CoA dehydrogenase deficiency
• Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
• The Utilization of Fatty Acids as Fuel Requires Three Stages of Processing
• ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN; ACADM
• Medium-chain acyl-coenzyme A dehydrogenase deficiency
• The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results
  

• Disorders of mitochondrial fatty acyl-CoA b-oxidation

• Medium-Chain Acyl-CoA Dehydrogenase Deficiency

• Medium-Chain Acyl-CoA Dehydrogenase Deficiency

• Role of carnitine in hepatic ketogenesis
• Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency

• Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD)

• Detection of urinary hexanoylglycine in the diagnosis of MCAD deficiency from newborn screening

• OMCFH/Newborn Metabolic Screening - Medium-Chain acyl-CoA Dehydrogenase

• In vivo kinetic studies in inborn errors of metabolism : expanding insights in (patho)physiology

• A general overview of the major metabolic pathways
• Fatty Acid Metabolism
• Metabolisme / Stofwisseling
• Honger respons

• DNA, ons erfelijk materiaal

books

• Medium-chain Acyl-CoEnzyme A Dehydrogenase Deficiency – James N. Parker & Philip M. Parker – ISBN 0-497-11255-8 – ICON Group International
• Advanced Nutrition and Human Metabolism (5^th edition) – Sareen S. Gropper, Jack L. Smith, James L. Groff – ISBN 978-0-495-11661-5 – Wadsworth Cengage Learning
• The Chemistry of Life (4^th edition) – Steven Rose – ISBN 978-0-14-027273-4 – Penguin Books
• Fats that heal, fats that kill – Udo Erasmus – ISBN 978-0-920470-38-1 – Alive Books
• Clinical paediatric dietetics (3^rd edition) – Vanessa Shaw, Margaret Lawson – ISBN 978-1-4051-3493-4 – Blackwell Publishing