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6. 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]
7. [Current problems in the diagnosis and treatment of phenylketonuria]. Sanielevici-Marinov S; Anagnoste V; Mark E; Tomescu E; Iordache C Pediatria (Bucur); 1973; 22(1):1-12. PubMed ID: 4733556 [No Abstract] [Full Text] [Related]
8. Glucagon stimulation of phenylalanine metabolism. The effects of acute and chronic glucagon treatment. Haley CJ; Harper AE Metabolism; 1982 Jun; 31(6):524-32. PubMed ID: 6123064 [TBL] [Abstract][Full Text] [Related]
9. [Importance of early diagnosis of phenylketonuria in women and control of phenylalanine levels during pregnancy]. Arrieta Blanco F; Bélanger Quintana A; Vázquez Martínez C; Martínez Pardo M Nutr Hosp; 2012; 27(5):1658-61. PubMed ID: 23478721 [TBL] [Abstract][Full Text] [Related]
10. Studies on the experimental phenylketonuria in rats. Iijima S; Ishii A; Miyakoshi T; Odaira T; Musha M Tohoku J Exp Med; 1975 Oct; 117(2):167-78. PubMed ID: 1209606 [TBL] [Abstract][Full Text] [Related]
11. Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia. Bartholomé K; Lutz P; Bickel H Pediatr Res; 1975 Dec; 9(12):899-903. PubMed ID: 1196708 [TBL] [Abstract][Full Text] [Related]
12. Nature of the molecular defect in phenylketonuria and hyperphenylalaninaemia. Friedman PA; Kaufman S; Kang ES Nature; 1972 Nov; 240(5377):157-9. PubMed ID: 4118080 [No Abstract] [Full Text] [Related]
13. [Hyperphenylalaninaemia with normal phenylalanine-hydroxylase activity and a deficiency of tetrahydrobiopterin and dihydropteridine reductase]. Rey F; Harpey JP; Leeming RJ; Blair JA; Aicardi J; Rey J Arch Fr Pediatr; 1977; 34(7 Suppl):CIX-CXX. PubMed ID: 931522 [TBL] [Abstract][Full Text] [Related]
14. Phenylalanine hydroxylase and tyrosine aminotransferase in human fetal and adult liver. Delvalle JA; Greengard O Pediatr Res; 1977 Jan; 11(1 Pt 1):2-5. PubMed ID: 12495 [TBL] [Abstract][Full Text] [Related]
15. Phenylketonuria: epitome of human biochemical genetics (second of two parts). Scriver CR; Clow CL N Engl J Med; 1980 Dec; 303(24):1394-400. PubMed ID: 7432385 [No Abstract] [Full Text] [Related]
16. Hyperphenylalaninemia due to a deficiency of biopterin. A variant form of phenylketonuria. Kaufman S; Berlow S; Summer GK; Milstien S; Schulman JD; Orloff S; Spielberg S; Pueschel S N Engl J Med; 1978 Sep; 299(13):673-9. PubMed ID: 683251 [TBL] [Abstract][Full Text] [Related]
18. [Aminoacid metabolism disorders in infancy with special reference to phenylketonuria. II. Aminoacid metabolism and general physiopathology of aminoacidopathies]. Segni G Minerva Nipiol; 1970; 20(4):83-110. PubMed ID: 4396023 [No Abstract] [Full Text] [Related]
19. Dietary phenylalanine and tyrosine interrelationships in the Sprague-Dawley rat. Elkin RG; Rogler JC; Featherston WR Proc Soc Exp Biol Med; 1981 Jul; 167(3):310-7. PubMed ID: 7255416 [No Abstract] [Full Text] [Related]
20. Comparative diagnostic value of phenylalanine challenge and phenylalanine hydroxylase activity in phenylketonuria. Hsieh MC; Berry HK; Bofinger MK; Phillips PJ; Guilfoile MB; Hunt MM Clin Genet; 1983 Jun; 23(6):415-21. PubMed ID: 6883786 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]