W. Oostheim

Alkyl-Dihydroxyacetonephosphate Synthase

Edwin C.J.M. de Vet, Lodewijk IJlst, W. Oostheim et al. · Journal of Biological Chemistry · 1998 · 120 citations · Full text

Molecular basis of hepatic carnitine palmitoyltransferase I deficiency.

Lodewijk IJlst, Hanna Mandel, W. Oostheim et al. · Journal of Clinical Investigation · 1998 · 94 citations · Full text

Genetics, Molecular Biology, Hepatic Carnitine Palmitoyltransferase +17

Mutational Spectrum of d-Bifunctional Protein Deficiency and Structure-Based Genotype-Phenotype Analysis

Sacha Ferdinandusse, Mari S. Ylianttila, Jolein Gloerich et al. · The American Journal of Human Genetics · 2005 · 93 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +7

Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low

M. E. J. den Boer, Lodewijk IJlst, Frits A. Wijburg et al. · Pediatric Research · 2000 · 59 citations · Full text

Common Lchad Mutation, Mendelian Disorder, Genetic Disorder +6

Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities

Edwin C.J.M. de Vet, Lodewijk IJlst, W. Oostheim et al. · Journal of Lipid Research · 1999 · 53 citations · Full text