Clinical, biochemical and genetic findings in two siblings with a dihydropyrimidinase deficiency-Reference-Cited by-同舟云学术

Clinical, biochemical and genetic findings in two siblings with a dihydropyrimidinase deficiency

Published:2007-06 Issue:2 Volume:91 Page:157-164
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

van Kuilenburg André B.P.,Meijer Judith,Dobritzsch Doreen,Meinsma Rutger,Duran Marinus,Lohkamp Bernhard,Zoetekouw Lida,Abeling Nico G.G.M.,van Tinteren Herman L.G.,Bosch Annet M.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference31 articles.

1. Dihydropyrimidine dehydrogenase and the efficacy and toxicity of 5-fluorouracil;van Kuilenburg;Eur. J. Cancer,2004

2. Familial pyrimidinemia and pyrimidinuria associated with severe fluorouracil toxicity;Tuchman;N. Engl. J. Med.,1985

3. Familial deficiency of dihydropyrimidine dehydrogenase. Biochemical basis for familial pyrimidinemia and severe 5-fluorouracil-induced toxicity;Diasio;J. Clin. Invest.,1988

4. Population and family studies of dihydropyrimidinuria: prevalence, inheritance mode, and risk of fluorouracil toxicity;Sumi;Am. J. Med. Genet.,1998

5. Dihydropyrimidinase deficiency and severe 5-fluorouracil toxicity;van Kuilenburg;Clin. Cancer Res.,2003

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