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2. Aromatic acid excretion in classical phenylketonuria and hyperphenylalaninemic variants. Koepp P; Hoffmann B Helv Paediatr Acta; 1974 Nov; 29(5):489-98. PubMed ID: 4452644 [No Abstract] [Full Text] [Related]
3. Urinary excretion of aromatic acids in hyperphenylalaninemic states: response to a protein challenge. Koepp P; Scholtyssek M; Plettner C Eur J Pediatr; 1978 Apr; 127(4):269-78. PubMed ID: 668711 [TBL] [Abstract][Full Text] [Related]
4. Influence of the phenylalanine dose on the aromatic acid excretion in phenylketonuric heterozygotes and controls after oral loading. Dahmann G; Olek K; Pravitz A; Wardenbach P Eur J Pediatr; 1978 Oct; 129(3):191-5. PubMed ID: 699924 [TBL] [Abstract][Full Text] [Related]
5. Aromatic acid excretion in phenylketonuria. Analysis of the unconjugated aromatic acids derived from phenylalanine. Blau K Clin Chim Acta; 1970 Jan; 27(1):5-18. PubMed ID: 5412612 [No Abstract] [Full Text] [Related]
6. Aromatic acids in urine of healthy infants, persistent hyperphenylalaninemia, and phenylketonuria, before and after phenylalanine load. Rampini S; Völlmin JA; Bosshard HR; Müller M; Curtius HC Pediatr Res; 1974 Jul; 8(7):704-9. PubMed ID: 4837567 [No Abstract] [Full Text] [Related]
7. The investigation of aromatic acids in phenylketonuria, alkaptonuria and tyrosinosis using gas-liquid chromatography. Hill A; Hoag GN; Zaleski WA Clin Chim Acta; 1972 Mar; 37():455-62. PubMed ID: 5022110 [No Abstract] [Full Text] [Related]
8. Quantitative analysis of phenylalanine metabolites in urine to detect heterozygotes of phenylketonuria. Olek K; Oyanagi K; Wardenbach P Humangenetik; 1974 Apr; 22(1):85-8. PubMed ID: 4837293 [No Abstract] [Full Text] [Related]
9. Gas chromatography of some urinary acid metabolites related to phenylketonuria. Hoffman NE; Gooding KM Anal Biochem; 1969 Oct; 31(1):471-9. PubMed ID: 5380714 [No Abstract] [Full Text] [Related]
10. [Relationship of urinary phenylpyruvate and o-hydroxyphenylacetate on serum phenylalanine level in patients with phenylketonuria treated by diet]. Zelnícek E; Sláma J; Podhradská O Cas Lek Cesk; 1975 Apr; 114(17):518-21. PubMed ID: 1131843 [No Abstract] [Full Text] [Related]
11. Statistical evaluation of a new method to detect carriers of phenylketonuria. Minami R; Olek K; Wardenbach P Humangenetik; 1975 Sep; 29(2):151-4. PubMed ID: 1236833 [TBL] [Abstract][Full Text] [Related]
12. [Relations between serum phenylalanine level and phenylpyruvate and o-hydroxyphenylacetate in urine of patients with phenylketonuria, treated by diet]. Zelnícek E; Podhradská O; Sláma J Bratisl Lek Listy; 1971; 55(1):63-9. PubMed ID: 5549026 [No Abstract] [Full Text] [Related]
13. [Phenylalanine metabolites in hyperphenylalaninemic children]. Alvarez Domínguez L; Campistol Plana J; Ribes Rubio A; Riverola de Vecina AT An Esp Pediatr; 1992 May; 36(5):371-4. PubMed ID: 1616197 [TBL] [Abstract][Full Text] [Related]
14. [The determination of ortho-hydroxyphenylacetic acid in the urine and its significance in the diagnosis of phenylketonuria]. Humbel R J Pharm Belg; 1967; 22(7):243-56. PubMed ID: 5609378 [No Abstract] [Full Text] [Related]
15. Gas chromatographic analysis of abnormal urinary organic acids in phenylketonuria. Hsiao KJ; Hung SH; Wu SJ; Yeh SF Taiwan Yi Xue Hui Za Zhi; 1985 Nov; 84(11):1240-50. PubMed ID: 3868699 [No Abstract] [Full Text] [Related]
16. Gas-liquid chromatography of phenylalanine metabolites in urine and sera of hyperphenylalaninemic and phenylketonuric patients. Kitagawa T Clin Chem; 1974 Dec; 20(12):1543-7. PubMed ID: 4430132 [No Abstract] [Full Text] [Related]
17. Gas-liquid chromatography of phenylalanine and its metabolites in serum and urine of various hyperphenylalaninemic subjects, their relatives, and controls. Kitagawa T; Smith BA; Brown ES Clin Chem; 1975 May; 21(6):735-40. PubMed ID: 1122617 [TBL] [Abstract][Full Text] [Related]
18. Quantitative studies on the urinary excretion of unconjugated aromatic acids in phenylketonuria. Chalmers RA; Watts RW Clin Chim Acta; 1974 Sep; 55(3):281-94. PubMed ID: 4415434 [No Abstract] [Full Text] [Related]
19. Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variants. Rey F; Pellié C; Sivy M; Blandin-Savoja F; Rey J; Frézal J Pediatr Res; 1974 May; 8(5):540-5. PubMed ID: 4151091 [No Abstract] [Full Text] [Related]
20. Measurement of phenyllactate, phenylacetate, and phenylpyruvate by negative ion chemical ionization-gas chromatography/mass spectrometry in brain of mouse genetic models of phenylketonuria and non-phenylketonuria hyperphenylalaninemia. Sarkissian CN; Scriver CR; Mamer OA Anal Biochem; 2000 May; 280(2):242-9. PubMed ID: 10790306 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]