M. E. J. den Boer

Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency: Clinical Presentation and Follow-Up of 50 Patients

M. E. J. den Boer, Ronald J. A. Wanders, Andrew A. M. Morris et al. · PEDIATRICS · 2002 · 189 citations

Long-Chain Fatty Acid Oxidation during Early Human Development

Nadia A. Oey, M. E. J. den Boer, Frits A. Wijburg et al. · Pediatric Research · 2005 · 98 citations · Full text

Metabolic Syndrome, Developmental Biology, Omega-3 Fatty Acid +7

Mitochondrial trifunctional protein deficiency: A severe fatty acid oxidation disorder with cardiac and neurologic involvement

M. E. J. den Boer, Carlo Dionisi‐Vici, Anupam Chakrapani et al. · The Journal of Pediatrics · 2003 · 90 citations

Mitochondrial Myopathy, Metabolic Syndrome, Cardiomyopathy +9

High activity of fatty acid oxidation enzymes in human placenta: Implications for fetal‐maternal disease

Nadia A. Oey, M. E. J. den Boer, Jos P.N. Ruiter et al. · Journal of Inherited Metabolic Disease · 2003 · 63 citations

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