Purine nucleoside phosphorylase deficiency associated with selective cellular immunodeficiency
Stoop, J W, Zegers, B J, Hendrickx, G F, van Heukelom, L H, Staal, G E, de Bree, P K, Wadman, S K, Ballieux, R E
Published in The New England journal of medicine (24.03.1977)
Published in The New England journal of medicine (24.03.1977)
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Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism
Duran, M, Rovers, P, de Bree, P K, Schreuder, C H, Beukenhorst, H, Dorland, L, Berger, R
Published in Journal of inherited metabolic disease (01.05.1991)
Published in Journal of inherited metabolic disease (01.05.1991)
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Dihydropyrimidinuria
Duran, M, Rovers, P, de Bree, P K, Schreuder, C H, Beukenhorst, H, Dorland, L, Berger, R
Published in The Lancet (British edition) (29.09.1990)
Published in The Lancet (British edition) (29.09.1990)
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Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?
Duran, M, Beemer, F A, van de Heiden, C, Korteland, J, de Bree, P K, Brink, M, Wadman, S K, Lombeck, I
Published in Journal of inherited metabolic disease (01.12.1978)
Published in Journal of inherited metabolic disease (01.12.1978)
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Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism
Berger, R., Vries, S.A.Stoker-de, Wadman, S.K., Duran, M., Beemer, F.A., de Bree, P.K., Weits-Binnerts, J.J., Penders, T.J., van der Woude, J.K.
Published in Clinica chimica acta (31.08.1984)
Published in Clinica chimica acta (31.08.1984)
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Diagnosis of inherited adenylosuccinase deficiency by thin-layer chromatography of urinary imidazoles and by automated cation exchange column chromatography of purines
de Bree, P.K., Wadman, S.K., Duran, M., de Jonge, H.Fabery
Published in Clinica chimica acta (15.05.1986)
Published in Clinica chimica acta (15.05.1986)
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O-Phosphohydroxylysinuria: a new inborn error of metabolism?
Dorland, L., Duran, M., De Bree, P.K., Smith, G.R., Horvath, A., Tibosch, A.S., Wadman, S.K.
Published in Clinica chimica acta (01.05.1990)
Published in Clinica chimica acta (01.05.1990)
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Azetidine-2-carboxylic acid contaminated dietary proline as a cause of urinary excretion of 4-amino-2-(S-cysteinyl)butyric acid in patients on oral treatment with a synthetic diet
Kamerling, J.P., Wadman, S.K., Duran, M., de Bree, P.K., Vliegenthart, J.F.G., Przyrembel, H., Bremer, H.J.
Published in Journal of chromatography (01.01.1983)
Published in Journal of chromatography (01.01.1983)
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Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism
Wadman, S K, Berger, R, Duran, M, de Bree, P K, Stoker-de Vries, S A, Beemer, F A, Weits-Binnerts, J J, Penders, T J, van der Woude, J K
Published in Journal of inherited metabolic disease (1985)
Published in Journal of inherited metabolic disease (1985)
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Linear relationship between the R- and S-enantiomers of β-aminoisobutyric acid in human urine
van Gennip, A.H., Kamerling, J.P., de Bree, P.K., Wadman, S.K.
Published in Clinica chimica acta (11.11.1981)
Published in Clinica chimica acta (11.11.1981)
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New defects of pyrimidine metabolism
Wadman, S K, Beemer, F A, de Bree, P K, Duran, M, van Gennip, A H, Ketting, D, van Sprang, F J
Published in Advances in experimental medicine and biology (1984)
Published in Advances in experimental medicine and biology (1984)
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Nϵ-(carboxymethyd)lysine, a constituent of human urine
Wadman, S.K., De Bree, P.K., Van Sprang, F.J., Kamerling, J.P., Haverkamp, J., Vliegenthart, J.F.G.
Published in Clinica chimica acta (24.03.1975)
Published in Clinica chimica acta (24.03.1975)
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