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Diagnosis of inherited adenylosuccinase deficiency by thin-layer chromatography of urinary imidazoles and by automated cation exchange column chromatography of purinesDE BREE, P. K; WADMAN, S. K; DURAN, M et al.Clinica chimica acta. 1986, Vol 156, Num 3, pp 279-287, issn 0009-8981Article

O-Phosphohydroxylysinuria : a new inborn error of metabolism ?DORLAND, L; DURAN, M; DE BREE, P. K et al.Clinica chimica acta. 1990, Vol 188, Num 3, pp 221-226, issn 0009-8981, 6 p.Article

Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolismBERGER, R; STOKER-DE VRIES, S. A; WADMAN, S. K et al.Clinica chimica acta. 1984, Vol 141, Num 2-3, pp 227-234, issn 0009-8981Article

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 dietKAMERLING, J. P; WADMAN, S. K; DURAN, M et al.Journal of chromatography. 1983, Vol 277, pp 41-51, issn 0021-9673Article