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2. [Hyperphenylalaninemia on account of biopterin deficiency. The phenylalanine hydroxylase complex and presentation of a patient with cofactor deficiency]. Beck B Ugeskr Laeger; 1983 Nov; 145(48):3725-7. PubMed ID: 6665886 [No Abstract] [Full Text] [Related]
3. Diagnosis and management of "malignant hyperphenylalaninemia". Cederbaum SD N Engl J Med; 1979 Aug; 301(8):441-2. PubMed ID: 460359 [No Abstract] [Full Text] [Related]
5. Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe. Wachtel U Hum Nutr Appl Nutr; 1986; 40 Suppl 1():61-9. PubMed ID: 3528074 [TBL] [Abstract][Full Text] [Related]
6. Phenylketonuria: epitome of human biochemical genetics (first of two parts). Scriver CR; Clow CL N Engl J Med; 1980 Dec; 303(23):1336-42. PubMed ID: 7001231 [No Abstract] [Full Text] [Related]
8. 'Mommy, why can't I have a hamburger like the other kids?'. Harding CO Gene Ther; 2000 Dec; 7(23):1969-70. PubMed ID: 11175306 [No Abstract] [Full Text] [Related]
9. A hypothesis on the biochemical mechanism of BH(4)-responsiveness in phenylalanine hydroxylase deficiency. Steinfeld R; Kohlschütter A; Ullrich K; Lukacs Z Amino Acids; 2003 Jul; 25(1):63-8. PubMed ID: 12836060 [TBL] [Abstract][Full Text] [Related]
10. Diseases of phenylalanine metabolism. Parker CE West J Med; 1979 Oct; 131(4):285-97. PubMed ID: 388868 [TBL] [Abstract][Full Text] [Related]
11. Kinetics of phenylalanine disappearance after intravenous load in phenylketonuria and its genetic variants. Rey F; Blandin-Savoja F; Rey J Pediatr Res; 1979 Jan; 13(1):21-5. PubMed ID: 431997 [No Abstract] [Full Text] [Related]
13. 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]
14. [Embryopathy due to maternal phenylketonuria: a cause of mental retardation]. Vázquez-López ME; Martínez-Regueira S; Pego-Reigosa R; González-Gómez FJ; Somoza-Rubio C; Morales-Redondo R Rev Neurol; 2006 Dec 1-15; 43(11):703-4. PubMed ID: 17133335 [No Abstract] [Full Text] [Related]
15. Genetic disorders involving recycling and formation of tetrahydrobiopterin. Kaufman S Adv Pharmacol; 1998; 42():41-3. PubMed ID: 9327841 [No Abstract] [Full Text] [Related]
16. Tetrahydrobiopterin protects phenylalanine hydroxylase activity in vivo: implications for tetrahydrobiopterin-responsive hyperphenylalaninemia. Thöny B; Ding Z; Martínez A FEBS Lett; 2004 Nov; 577(3):507-11. PubMed ID: 15556637 [TBL] [Abstract][Full Text] [Related]
17. [A mother with hyperphenylalaninemia and development of the fetus during a diet in pregnancy]. Blehová B; Finková A; Pazoutová N Cesk Gynekol; 1977 Jul; 42(6):453-4. PubMed ID: 890779 [No Abstract] [Full Text] [Related]
18. [Congenital disorders of phenylalanine metabolism]. Rampini S Schweiz Med Wochenschr; 1973 Apr; 103(15):537-46. PubMed ID: 4572324 [No Abstract] [Full Text] [Related]