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American Journal of Surgery|November 1, 1994
A prospective longitudinal study on radiation-induced hearing lossL J Anteunis, S L Wanders, J J Hendriks, et al.JIMD Reports|February 23, 2013
Zellweger Spectrum Disorder with Mild Phenotype Caused by PEX2 Gene MutationsAndrea Mignarri, Claudia Vinciguerra, Antonio Giorgio, et al.Journal of Inherited Metabolic Disease|December 15, 2022
Genetic defects in peroxisome morphogenesis (Pex11β, dynamin-like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid-phospholipid metabolismYuichi Abe, Ronald J A Wanders, Hans R Waterham, et al.Acta Biologica Et Medica Germanica|January 1, 1981
Control mechanisms of energy-dependent metabolic pathways in hepatocytesJ M Tager, R J Wanders, A K Groen, et al.Journal of Inherited Metabolic Disease|November 8, 2003
Stereoselective analysis of 2-hydroxysebacic acid in urine of patients with Zellweger syndrome and of premature infants fed with medium-chain triglyceridesA Muth, A Mosandl, R J A Wanders, et al.FEBS Letters|May 9, 2006
Identification and characterization of human cardiolipin synthaseRiekelt H Houtkooper, Hana Akbari, Henk van Lenthe, et al.The Journal of Pediatrics|July 25, 2006
Pitfalls of neonatal screening for very-long-chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometryIna Schymik, Michaela Liebig, Martina Mueller, et al.Molecular Genetics and Metabolism|December 14, 2007
Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidationMalika Chegary, Heleen Te Brinke, Mirjam Doolaard, et al.FEBS Letters|March 21, 2006
Peroxisomal trans-2-enoyl-CoA reductase is involved in phytol degradationJ Gloerich, J P N Ruiter, D M van den Brink, et al.Placenta|November 23, 2005
L-carnitine is synthesized in the human fetal-placental unit: potential roles in placental and fetal metabolismN A Oey, N van Vlies, F A Wijburg, et al.Pageof 132