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5. HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE. KOMROWER GM; WILSON V; CLAMP JR; WESTALL RG Arch Dis Child; 1964 Jun; 39(205):250-6. PubMed ID: 14169454 [No Abstract] [Full Text] [Related]
6. Abnormalities of tryptophan metabolism (kynurenine pathway) found in a group of 830 mentally retarded children. Sabater J; Ricós C Clin Chim Acta; 1974 Oct; 56(2):175-86. PubMed ID: 4434630 [No Abstract] [Full Text] [Related]
7. Familial hyperprolinemia and mental retardation. A second metabolic type. Selkoe DJ Neurology; 1969 May; 19(5):494-502. PubMed ID: 5815222 [No Abstract] [Full Text] [Related]
8. Inborn errors of metabolism associated with unusual odors. Carpenter DG; Carter CH J Fla Med Assoc; 1970 May; 57(5):31-3. PubMed ID: 5449191 [No Abstract] [Full Text] [Related]
9. [Studies on tryptophan metabolism in oligophrenic children. 1. Results on the excretion of kynurenic acid and xanthurenic acid following administration of tryptophan and their dependence on vitamin B 6 supply]. Schulz M; Grimm U; Schmitz W; Knapp A Psychiatr Neurol Med Psychol (Leipz); 1973 Feb; 25(2):98-106. PubMed ID: 4713451 [No Abstract] [Full Text] [Related]
11. [Recent studies on a genetic disorder of tryptophan metabolism and its relations to vitamin B6]. Knapp A Dtsch Z Verdau Stoffwechselkr; 1965 Oct; 25(4):252-3. PubMed ID: 5888914 [No Abstract] [Full Text] [Related]
12. The effect of burns on the metabolism of tryptophan in children. Barlow GB; Wilkinson AW Clin Chim Acta; 1972 Oct; 41():169-74. PubMed ID: 4645231 [No Abstract] [Full Text] [Related]
13. Screening for defects in tryptophan metabolism. Marklová E; Makovicková H; Krákorová I J Chromatogr A; 2000 Feb; 870(1-2):289-93. PubMed ID: 10722086 [TBL] [Abstract][Full Text] [Related]
14. Excretion of kynurenic acid and xanthurenic acid during infection. Shaw RC; Feigin RD Pediatrics; 1971 Jan; 47(1):47-56. PubMed ID: 5545403 [No Abstract] [Full Text] [Related]