P. Vreken
Amsterdam UMC Location University of Amsterdam(NL)Emma Kinderziekenhuis(NL)University of Amsterdam(NL)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Biochemical and Molecular Research, Peroxisome Proliferator-Activated Receptors, Neonatal Health and Biochemistry, Mitochondrial Function and Pathology
Most-Cited Works
- → Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth Syndrome(2000)372 cited
- Clinical implications of dihydropyrimidine dehydrogenase (DPD) deficiency in patients with severe 5-fluorouracil-associated toxicity: identification of new mutations in the DPD gene.(2000)
- → Mutations in the 3β-Hydroxysterol Δ24-Reductase Gene Cause Desmosterolosis, an Autosomal Recessive Disorder of Cholesterol Biosynthesis(2001)353 cited
- → Smith-Lemli-Opitz Syndrome Is Caused by Mutations in the 7-Dehydrocholesterol Reductase Gene(1998)294 cited
- → Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency(1999)282 cited
- → Disorders of mitochondrial fatty acyl‐CoA β‐oxidation(1999)261 cited
- → Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy(2000)252 cited