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| 1 | Identification of novel point mutations in the dihydropyrimidine dehydrogenase gene显示文摘 | Vreken P Van Kuilenburg ABP Meinsma R | 1997 | J Inher Metab Dis1997，20，： | 1 |
| 2 | Genotype and phenotype in patients with dihydropyfimidine dehydrogenase deficiency 显示文摘 | Van Kuilenburg AB Vreken P Abeling NG | 1999 | Hum Genet1999，104，： | 1 |
| 3 | Identification of a four-base deletion (del TCAT296-299) in the dihydropyrimidine dehydrogenase gene with variable clinical expression显示文摘 | Vreken P Van Kuilenburg ABP Meinsma R | 1997 | Hum Genet1997，100，： | 1 |
| 4 | A New Generation of 'DELUX' Flourescent Lamps:An Efficiency of 80 Lumens/W or More a Color Rendering Index of Approximately 85显示文摘 | Verstegen J M P J Radielovic D Vreken L E | 1974 | J Electrochem Soc1974，121，12： | 1 |
| 5 | Characterization of calcium phosphate cements modified by addition of amorphous calcium phosphate 显示文摘 | Natasja M F Van den Vreken Ilse Y | 2010 | Acta Biomaterialia2010，2，6： | 1 |
| 6 | Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency显示文摘 | Van Kuilenburg ABP Vreken P Abeling NGGM | 1999 | Hum Genet1999，104，： | 1 |
| 7 | Significantly reduced docosahexaenoic and docosapentaenoic acid concentrations in erythrocyte membranes from schizophrenic patients compared with a carefully matched control group显示文摘 | Assies J Lieverse R Vreken P | 2001 | Biol Psychiatry2001，49，6： | 1 |
| 8 | Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency 显示文摘 | VAN KUILENBURG A B VREKEN P ABELING N G | 1999 | Hum Genet1999，104，1： | 1 |
| 9 | Dihydropyrimidine dehydrogenase(DPD) deficiency:identification and expression of missense mutations C29R,R886H and R235W显示文摘 | Vreken P A Meinsma R | 1997 | Hum Genet1997，101，3： | 1 |
| 10 | Genotype and phenotype in patients with dihydropyrimidine dehydrogenase defieiency显示文摘 | van Kuilenburg AB Vreken P AbeIing N(-} eta| | 1999 | Hum Genet1999，104，1： | 1 |
| 11 | Nomenclature for human DPYD alleles 显示文摘 | Mcleod HL Collie-Duguid ESR Vreken P | 1998 | Pharmaeogenetics1998，8，6： | 1 |
| 12 | Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases 显示文摘 | WANDERS R J VREKEN P FERDINANDUSSE S | 2001 | Biochem Soc Trans2001，29，2： | 1 |
| 13 | Isolation, proliferation and differ entiation of osteoblastic cells to study cellfoiomaterial interactions:comparison of different isolation techniques and source 显示文摘 | Heidi Declercq Natasja Van den Vreken Ema De Maeyer | 2004 | Biomaterials2004，25，5： | 1 |
| 14 | Peroxisomal fatty acid alpha-and beta-oxidation in humans : enzymology, peroxisomal metabolite transpor- ters and peroxisomal diseases 显示文摘 | Wanders R J Vreken P Ferdinandusse S | 2001 | Biochem Soc Trans2001，29，： | 1 |
| 15 | Isolation,proliferation and differ entiation of osteoblastic cells to study cell/biomaterial interactions:comparison of different isolation techniques and source显示文摘 | Declercq H Van den Vreken N De Maeyer E | 2004 | Biomaterials2004，25，5： | 1 |
| 16 | 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 |
| 17 | Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome 显示文摘 | Vreken P Valianpour F Nijtmans LG | 2000 | Biochem Biophys Res Commun2000，279，2： | 1 |
| 18 | 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 |
| 19 | Nomenclature for human DPYD alleles 显示文摘 | MCLEOD HL COLLIE-DUGUID ES VREKEN P | 1998 | Pharmacogenetics1998，8，6： | 1 |
| 20 | Evaluation of tRNA Intergenic length polymorphism (tDNA-PCR) for the differentiation of the members of the Burkholderia cepacia complex显示文摘 | Storms V Vreken N Vandemme P | 2002 | Systematic and Applied Microbiology2002，25，： | 1 |
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