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G.H. van Lenthe
G.H. van Lenthe
University of Amsterdam
Dihydropyrimidine dehydrogenase
Fluorouracil
Biochemistry
Point mutation
Loss of heterozygosity
4
Papers
160
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Detection of beta-ureidopropionase deficiency with HPLC-electrospray tandem mass spectrometry and confirmation of the defect at the enzyme level.
2001
Journal of Inherited Metabolic Disease
A. B. P. van Kuilenburg
G.H. van Lenthe
B. Assmann
Gudrun Göhlich-Ratmann
Georg F. Hoffmann
Christa Bräutigam
R.A. Wevers
A. H. van Gennip
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Citations (17)
Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity.
1998
Advances in Experimental Medicine and Biology
A. B. P. van Kuilenburg
Peter Vreken
Louk V. A. M. Beex
Rutger Meinsma
G.H. van Lenthe
R.A. de Abreu
A. H. van Gennip
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Citations (10)
Dihydropyrimidinase deficiency: Confirmation of the enzyme defect in dihydropyrimidinuria
1997
Journal of Inherited Metabolic Disease
A. H. van Gennip
R.A. de Abreu
G.H. van Lenthe
J. A. J. M. Bakkeren
Jan J. Rotteveel
Peter Vreken
A. B. P. van Kuilenburg
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Citations (31)
Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity
1997
European Journal of Cancer
A. B. P. van Kuilenburg
Peter Vreken
Louk V. A. M. Beex
Rutger Meinsma
G.H. van Lenthe
R.A. de Abreu
A. H. van Gennip
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Citations (102)
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