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Biochimica Et Biophysica Acta|April 27, 2016
The impact of altered carnitine availability on acylcarnitine metabolism, energy expenditure and glucose tolerance in diet-induced obese miceMarieke G Schooneman, Riekelt H Houtkooper, Carla E M Hollak, et al.Journal of Inherited Metabolic Disease|February 22, 2012
Clinical variability of isovaleric acidemia in a genetically homogeneous populationM Dercksen, M Duran, L Ijlst, et al.Journal of Lipid Research|October 4, 2006
Metabolism of phytol to phytanic acid in the mouse, and the role of PPARalpha in its regulationJ Gloerich, D M van den Brink, J P N Ruiter, et al.Pediatrics|February 4, 2003
Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrumViola Prietsch, Ertan Mayatepek, Hermann Krastel, et al.Acta Paediatrica (Oslo, Norway : 1992)|August 7, 2002
Long-chain 3-hydroxyacylCoA dehydrogenase deficiency: a new case presenting with liver dysfunction, cholestasis and fibrosisM H Odievre, C Sevin, J Laurent, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 26, 2008
Increased intramyocellular lipid content but normal skeletal muscle mitochondrial oxidative capacity throughout the pathogenesis of type 2 diabetesHenk M De Feyter, Ellen Lenaers, Sander M Houten, et al.Journal of Inherited Metabolic Disease|June 10, 2006
Carnitine supplementation induces long-chain acylcarnitine production--studies in the VLCAD-deficient mouseM Liebig, M Gyenes, G Brauers, et al.Molecular Genetics and Metabolism|April 20, 2006
High incidence of hyperoxaluria in generalized peroxisomal disordersChristiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.Biochimica Et Biophysica Acta|July 16, 2013
Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficientSara Violante, Lodewijk Ijlst, Heleen Te Brinke, et al.Annals of Neurology|August 10, 2010
Mutations in PEX10 are a cause of autosomal recessive ataxiaLuc Régal, Merel S Ebberink, Nathalie Goemans, et al.Pageof 48