Pyrimidine degradation defects and severe 5-fluorouracil toxicity (Q35967209)

11 August 2017

1 reference

title

Pyrimidine degradation defects and severe 5-fluorouracil toxicity (English)

1 reference

11 August 2017

1 reference

van Kuilenburg AB

1

1 reference

11 August 2017

Meinsma R

series ordinal

2

1 reference

11 August 2017

van Gennip AH

series ordinal

3

1 reference

11 August 2017

language of work or name

1 reference

1 October 2004

1 reference

Nucleosides, Nucleotides & Nucleic Acids

11 August 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

11 August 2017

volume

23

1 reference

11 August 2017

issue

8-9

1 reference

11 August 2017

page(s)

1371-1375

1 reference

Pharmacogenetic and clinical aspects of dihydropyrimidine dehydrogenase deficiency

11 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

Reduced 5-FU clearance in a patient with low DPD activity due to heterozygosity for a mutant allele of the DPYD gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

Increased risk of grade IV neutropenia after administration of 5-fluorouracil due to a dihydropyrimidine dehydrogenase deficiency: high prevalence of the IVS14+1g>a mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

Dihydropyrimidine dehydrogenase deficiency and fluorouracil-related toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

High prevalence of the IVS14 + 1G>A mutation in the dihydropyrimidine dehydrogenase gene of patients with severe 5-fluorouracil-associated toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

Population and family studies of dihydropyrimidinuria: prevalence, inheritance mode, and risk of fluorouracil toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

Dihydropyrimidinase deficiency: structural organization, chromosomal localization, and mutation analysis of the human dihydropyrimidinase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FNCN-200027624

21 January 2018

Identifiers

DOI

10.1081/NCN-200027624

1 reference

11 August 2017

1 reference