Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes

Tandem Mass Spectrometry

Fred W. McLafferty · 2008 · 648 citations

Biochemistry, Clinical Mass Spectrometry, Mass Spectrometry +7

Carnitine metabolism in the fasting rat.

Eric P. Brass, Charles L. Hoppel · Journal of Biological Chemistry · 1978 · 301 citations · Full text

Animal Physiology, Carnitine Metabolism, Energy Metabolism +13

Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Children with Non-Ketotic Hypoglycemia and Low Carnitine Levels

Charles A. Stanley, Daniel E. Hale, Paul M. Coates et al. · Pediatric Research · 1983 · 197 citations · Full text

Nutrition, Metabolic Syndrome, Metabolic Disorder +8

Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria

Niels Gregersen, Runa Lauritzen, Karsten Boye Rasmussen · Clinica Chimica Acta · 1976 · 132 citations

Suberylglycine Excretion, Dicarboxylic Aciduria, Urology +4

Diagnostic and Therapeutic Implications of Medium-Chain Acylcarnitines in the Medium-Chain Acyl-CoA Dehydrogenase Deficiency

Charles R. Roe, David S. Millington, David Maltby et al. · Pediatric Research · 1985 · 128 citations · Full text

Biosynthesis, Aldo-keto Reductase, Aldehyde Dehydrogenase +9