P. A. W. Mooyer

A Lethal Defect of Mitochondrial and Peroxisomal Fission

Hans R. Waterham, Janet Koster, Carlo W.T. van Roermund et al. · New England Journal of Medicine · 2007 · 743 citations

Life Sciences, Genetics, Neuroscience +17

Autosomal Recessive HEM/Greenberg Skeletal Dysplasia Is Caused by 3β-Hydroxysterol Δ14-Reductase Deficiency Due to Mutations in the Lamin B Receptor Gene

Hans R. Waterham, Janet Koster, P. A. W. Mooyer et al. · The American Journal of Human Genetics · 2003 · 214 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Clinical and biochemical spectrum of D‐bifunctional protein deficiency

Sacha Ferdinandusse, Simone Denis, P. A. W. Mooyer et al. · Annals of Neurology · 2005 · 195 citations

Life Sciences, Biochemistry, Pediatrics +17

ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism

Sacha Ferdinandusse, Kim D. Falkenberg, Janet Koster et al. · Journal of Medical Genetics · 2016 · 120 citations · Full text

Life Sciences, Biochemistry, Genetics +17

Plasmalogens participate in very-long-chain fatty acid-induced pathology

Pedro Brites, P. A. W. Mooyer, L. el Mrabet et al. · Brain · 2008 · 111 citations · Full text

Life Sciences, Biochemistry, Cell Biology +17