Concepedia

Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism

M. Durán, P. Rovers, P.K. De Bree, C. H. Schreuder, H. Beukenhorst, L. Dorland, Rolf M.F. Berger

Journal of Inherited Metabolic Disease · 1991 · 54 citations · 7 references

DOI

Concepts

References

7

Familial deficiency of dihydropyrimidine dehydrogenase. Biochemical basis for familial pyrimidinemia and severe 5-fluorouracil-induced toxicity.

Robert B. Diasio, T L Beavers, John T. Carpenter · Journal of Clinical Investigation · 1988 · 500 citations · Full text

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Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiency

J. A. J. M. Bakkeren, Ronney A. De Abreu, R. C. A. Sengers et al. · Clinica Chimica Acta · 1984 · 101 citations

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Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism

Rolf M.F. Berger, S. A. Stoker‐de Vries, S.K. Wadman et al. · Clinica Chimica Acta · 1984 · 100 citations · Full text

, , +9

Purification and properties of 5,6‐dihydropyrimidine amidohydrolase from calf liver

Jürgen KAUTZ, Klaus D. Schnackerz · European Journal of Biochemistry · 1989 · 45 citations · Full text

, , +16

Diagnosis of inherited adenylosuccinase deficiency by thin-layer chromatography of urinary imidazoles and by automated cation exchange column chromatography of purines

P.K. De Bree, S.K. Wadman, M. Durán et al. · Clinica Chimica Acta · 1986 · 40 citations

, , +8