Simple method for the quantitative analysis of dihydropyrimidines and N-carbamyl-beta-amino acids in urine.

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作者信息

van Gennip A H, Busch S, Scholten E G, Stroomer L E, Abeling N G

机构信息

Dept. of Pediatrics, University Hospital AMC, Amsterdam, The Netherlands.

出版信息

Adv Exp Med Biol. 1991;309B:15-9. doi: 10.1007/978-1-4615-7703-4_4.

DOI:10.1007/978-1-4615-7703-4_4

PMID:1781359

Abstract

摘要

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Simple method for the quantitative analysis of dihydropyrimidines and N-carbamyl-beta-amino acids in urine.

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引用本文的文献

1H NMR spectroscopy of body fluids in patients with inborn errors of purine and pyrimidine metabolism.

J Inherit Metab Dis. 1997 Jul;20(3):345-50. doi: 10.1023/a:1005313524869.

Screening for defects of dihydropyrimidine degradation by analysis of amino acids in urine before and after acid hydrolysis.

J Inherit Metab Dis. 1992;15(3):413-5. doi: 10.1007/BF02435991.

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相似文献

Simple method for the quantitative analysis of dihydropyrimidines and N-carbamyl-beta-amino acids in urine.

Adv Exp Med Biol. 1991;309B:15-9. doi: 10.1007/978-1-4615-7703-4_4.

Clinical and biochemical aspects of dihydropyrimidinase deficiency.

Adv Exp Med Biol. 1998;431:125-8. doi: 10.1007/978-1-4615-5381-6_24.

Screening and diagnosis of beta-ureidopropionase deficiency by gas chromatographic/mass spectrometric analysis of urine.

J Mass Spectrom. 2002 Sep;37(9):954-62. doi: 10.1002/jms.354.

Dihydropyrimidinuria: the first case in Japan.

Adv Exp Med Biol. 1994;370:383-6. doi: 10.1007/978-1-4615-2584-4_83.

Screening for defects of dihydropyrimidine degradation by analysis of amino acids in urine before and after acid hydrolysis.

J Inherit Metab Dis. 1992;15(3):413-5. doi: 10.1007/BF02435991.

New defects of pyrimidine metabolism.

Adv Exp Med Biol. 1984;165 Pt A:109-14. doi: 10.1007/978-1-4684-4553-4_19.

Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiency.

Medicine (Baltimore). 2019 Jan;98(1):e14021. doi: 10.1097/MD.0000000000014021.

Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism.

J Inherit Metab Dis. 1991;14(3):367-70. doi: 10.1007/BF01811705.

Urinary excretion of purine and pyrimidine metabolites in the neonate.

Pediatr Res. 1993 Dec;34(6):762-6. doi: 10.1203/00006450-199312000-00012.

Clinical and biochemical findings in six patients with pyrimidine degradation defects.

J Inherit Metab Dis. 1994;17(1):130-2. doi: 10.1007/BF00735416.

引用本文的文献

1H NMR spectroscopy of body fluids in patients with inborn errors of purine and pyrimidine metabolism.

J Inherit Metab Dis. 1997 Jul;20(3):345-50. doi: 10.1023/a:1005313524869.

Screening for defects of dihydropyrimidine degradation by analysis of amino acids in urine before and after acid hydrolysis.

J Inherit Metab Dis. 1992;15(3):413-5. doi: 10.1007/BF02435991.