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| 1 | Peroxisomes, lipid metabolism, and peroxisomal disorders 显示文摘 | Wanders RJ | 2004 | Mol Genet Metab2004，83，12： | 1 |
| 2 | Phytanic acid metabolism inhealth and disease显示文摘 | Wanders RJ Komen J Ferdinandusse S | 2011 | Biochim Biophys Acta2011，1811，9： | 1 |
| 3 | Disorders of mitochondrial fatty acyl-CoA beta-oxidation 显示文摘 | Wanders RJ Yreken P denoer ME | 1999 | J Inherit Metab Dis1999，22，4： | 1 |
| 4 | X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy显示文摘 | Geel BM Assies J Wanders RJ | 1997 | Journal of Neurology Neurosurgery and Psychiatry1997，63，1： | 1 |
| 5 | CelluLar and molecular effects of sirtuins in health and disease显示文摘 | Wanders RJ Komen J Ferdinandusse S | | 0，，09： | 1 |
| 6 | Cerebral palsy and pyruvate dehydrogenase deficiency:identification of two new mutations in the E1alpha,gene显示文摘 | Lissens W,Vreken P,Barth PG,Wijburg FA,Ruitenbeek W,Wanders RJ, | 1999 | Eur J1999，15，10： | 1 |
| 7 | Disorders of mitochondrial fatty acyl-CoA b-oxidation显示文摘 | Wanders RJ Vreken P den Boer ME | 1999 | J Inherit Metab Dis1999，22，： | 1 |
| 8 | Molecularbasisoflongchain3-hydroxyacyl-CoA dehydrogenase deficiency:identification of the major disease-causing mutation in the alpha-subunit of the mito-chondrial trifunctional protein显示文摘 | Ijlst L Wanders RJ Ushikubo S | 1994 | Biochim Biophys Acta1994，1215，： | 1 |
| 9 | A case of methemoglobinemia type Ⅱ due to NADH-cytochrome b5 reductase deficiency:determination of the molecular basis显示文摘 | Aalfs CM Salieb-Beugelaar GB Wanders RJ | 2000 | Hum Mutat2000，16，1： | 1 |
| 10 | acephalopathy显示文摘 | Bischof F Nagele T Wanders RJ 3-hydroxy-3- methylglutaryl-CoA lyase deficiency in an adult with leukoe | 2004 | Ann Neurol2004，56，5： | 1 |
| 11 | Disorders of mitochondrial fatty acyl- CoA beta- oxidation显示文摘 | Wanders RJ Vreken P Wijburg FA | 1999 | J Inherit Metab Dis1999，22，： | 1 |
| 12 | The Secret life of NAD + : an old metabolite controlling new metabolic signaling path- ways显示文摘 | Houtkooper RH Canto C Wanders RJ | 2010 | Endocrine Rev2010，31，2： | 1 |
| 13 | Carnitine biosynthesis in mammals显示文摘 | Vaz FM Wanders RJ | 2002 | Bio- chem J2002，361，3： | 1 |
| 14 | Molecular basis of Refsum disease:sequence variations in phytanoyl-CoA hydroxylase (PHYH) and the PTS2 receptor(PEX7)显示文摘 | Jansen GA Waterham HR Wanders RJ | 2004 | Hum Mutat2004，23，3： | 1 |
| 15 | X-linked adrenoleukodystrophy:clinical presentation,diagnosis and theray显示文摘 | Geel BM Asaies J Wanders RJ | 1997 | Neurol Neurosurg Psychiatry1997，63，1： | 1 |
| 16 | Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy显示文摘 | Linnebank M Kemp S Wanders RJ | | 0，，03： | 1 |
| 17 | Molecular basis of Refsum disease: sequence variations in phytanoyl-CoA hydroxylase (PHYH) and the PTS2 receptor (PEXT) 显示文摘 | Jansen GA Waterham HR Wanders RJ | 2004 | Hum Mutat2004，23，3： | 1 |
| 18 | The secret life of NAD+:an old metaholite controlling new metabolic signaling pathways显示文摘 | Houtkooper RH Cantó C Wanders RJ | | 0，，： | 1 |
| 19 | Peroxisomes, lipid metabolism and lipotoxicity显示文摘 | Wanders RJ Ferdinandusse S Brites P | 2010 | Biochim Biophys Acta2010，1801，3： | 1 |
| 20 | Mammalian peroxisomal ABC transporters:from endogenous substrates to pathology and clinical significance显示文摘 | Kemp S Theodoulou FL Wanders RJ | 2011 | Br J Pharmacol2011，164，7： | 1 |
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