Dihydropyrimidinuria without clinical symptoms

Journal of Inherited Metabolic Disease

Volumn 19, Issue 5, 1996, Pages 701-702

  Sumi, S ^a  

^a Nagoya City Child Welfare Center   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DIHYDROPYRIDINE;

ADULT; AMINO ACID ANALYSIS; ARTICLE; CONTROLLED STUDY; CONVULSION; FEMALE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; METABOLIC DISORDER; PYRIMIDINE METABOLISM; SCREENING TEST; URINALYSIS;

EID: 0029791070     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01799851     Document Type: Article

References (4)

1. Duran M, Rovers P, de Bree PK, Schreuder CH, Beukenhorst H, Dorland L (1990) Dihydropyrimidinuria. Lancet 336: 817-818.
2. Henderson MJ, Ward K, Simmonds HA, Duley JA, Davies PM ( 1993) Dihydropyrimidinase deficiency presenting in infancy with severe developmental delay. J Inker Metab Dis 16: 574-576
3. Ohba S, Kidouchi K, Sumi S, et al (1995) Dihydropyrimidinuria: first case in Japan. Adv Med Biol 370: 383-386.
4. Sumi S, Kidouchi K, Ohba S, Wada Y (1995) Automated screening system for purine and pyrimidine metabolism disorders using high-performance liquid chromatography. J Chromatogr 672: 233-240.