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Annals of Neurology|October 27, 2004
3-hydroxy-3-methylglutaryl-CoA lyase deficiency in an adult with leukoencephalopathyFelix Bischof, Thomas Nägele, Ronald J A Wanders, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2008
Characterization of the human omega-oxidation pathway for omega-hydroxy-very-long-chain fatty acidsRobert-Jan Sanders, Rob Ofman, Georges Dacremont, et al.
Frontiers in Endocrinology|December 17, 2021
Nutritional Regulation of Hepatic FGF21 by Dietary Restriction of MethionineHan Fang, Kirsten P Stone, Laura A Forney, et al.
Frontiers in Nutrition|October 14, 2022
Protein quality of soy and the effect of processing: A quantitative reviewLisa A van den Berg, Jurriaan J Mes, Marco Mensink, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Signals on proteins, intracellular targeting and inborn errors of organellar metabolismJ M Tager, J M Aerts, C van den Bogert, et al.
Physiological Reviews|August 11, 2022
The physiological functions of human peroxisomesRonald J A Wanders, Myriam Baes, Daniela Ribeiro, et al.
Annual Review of Nutrition|May 19, 2022
The Origins, Evolution, and Future of Dietary Methionine RestrictionHan Fang, Kirsten P Stone, Desiree Wanders, et al.
The Journal of Pediatrics|October 1, 2003
MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiencyUte Spiekerkoetter, Bin Sun, Thomas Zytkovicz, et al.
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