(Q43693774)

English

Simple gas chromatographic-mass spectrometric procedure for diagnosing pyrimidine degradation defects for prevention of severe anticancer side effects

scientific article published in July 2001

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 November 2017

Simple gas chromatographic-mass spectrometric procedure for diagnosing pyrimidine degradation defects for prevention of severe anticancer side effects (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

author name string

Kuhara T

1

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Europe PubMed Central

PubMed publication ID

25 November 2017

Ohdoi C

2

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Europe PubMed Central

PubMed publication ID

25 November 2017

Ohse M

3

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Europe PubMed Central

PubMed publication ID

25 November 2017

publication date

1 July 2001

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Europe PubMed Central

PubMed publication ID

25 November 2017

Journal of Chromatography B: Biomedical Sciences and Applications

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Europe PubMed Central

PubMed publication ID

25 November 2017

758

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Europe PubMed Central

PubMed publication ID

25 November 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

61-74

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Inborn errors of pyrimidine degradation: Clinical, biochemical and molecular aspects

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

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7 January 2021

based on heuristic

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Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0378-4347%2801%2900143-8

7 January 2021

based on heuristic

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Dihydropyrimidinase deficiency presenting in infancy with severe developmental delay.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-4347%2801%2900143-8

7 January 2021

based on heuristic

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Dihydropyrimidinuria: The First Case in Japan

1 reference

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7 January 2021

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

1 reference

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7 January 2021

based on heuristic

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Molecular basis of the human dihydropyrimidine dehydrogenase deficiency and 5-fluorouracil toxicity

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Comparative study of thymine and uracil metabolism in healthy persons and in a patient with dihydropyrimidine dehydrogenase deficiency

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Automated determination of orotic acid, uracil and pseudouridine in urine by high-performance liquid chromatography with column switching

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Two-dimensional thin-layer chromatography for the screening of disorders of purine and pyrimidine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0378-4347%2801%2900143-8

7 January 2021

based on heuristic

inferred from DOI database lookup

New defects of pyrimidine metabolism

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

A new chemical diagnostic method for inborn errors of metabolism by mass spectrometry-rapid, practical, and simultaneous urinary metabolites analysis

1 reference

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Automated screening of urine samples for carbohydrates, organic and amino acids after treatment with urease

1 reference

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based on heuristic

inferred from DOI database lookup

Automated screening system for purine and pyrimidine metabolism disorders using high-performance liquid chromatography

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Pilot study of gas chromatographic-mass spectrometric screening of newborn urine for inborn errors of metabolism after treatment with urease

1 reference

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Urine screening of five-day-old newborns: metabolic profiling of neonatal galactosuria

1 reference

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7 January 2021

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Differential diagnosis of homocystinuria by urease treatment, isotope dilution and gas chromatography-mass spectrometry

1 reference

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7 January 2021

based on heuristic

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Hyper-beta-alaninemia associated with beta-aminoaciduria and gamma-aminobutyricaciduaia, somnolence and seizures

1 reference

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7 January 2021

based on heuristic

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Pyridoxine-responsive hyper-beta-alaninemia associated with Cohen's syndrome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Deficiency of d-β-aminoisobutyrate: Pyruvate aminotransferase in the liver of genetic high excretors of d-β-aminosobutyrate

1 reference

https://api.crossref.org/works/10.1016%2FS0378-4347%2801%2900143-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Urinary uracil concentrations are a useful guide to genetic disorders associated with neurological deficits and abnormal pyrimidine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0378-4347%2801%2900143-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0378-4347(01)00143-8

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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