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10. Tetrahydrobiopterin and inherited hyperphenylalaninemias. Blau N; Thony B; Spada M; Ponzone A Turk J Pediatr; 1996; 38(1):19-35. PubMed ID: 8819618 [TBL] [Abstract][Full Text] [Related]
11. [Interpretation of the consensus about the diagnosis and treatment of hyperphenylalaninemia]. Ye J; Gu X Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):430-2. PubMed ID: 25190162 [No Abstract] [Full Text] [Related]
12. Successful treatment of phenylketonuria with tetrahydrobiopterin. Trefz FK; Aulela-Scholz C; Blau N Eur J Pediatr; 2001 May; 160(5):315. PubMed ID: 11388602 [No Abstract] [Full Text] [Related]
13. Tetrahydrobiopterin deficiency and an international database of patients. Blau N; Dhondt JL Adv Exp Med Biol; 1993; 338():255-61. PubMed ID: 8304121 [No Abstract] [Full Text] [Related]
17. Unsolved problems in diagnosis and therapy of hyperphenylalaninemia caused by defects in tetrahydrobiopterin metabolism. Kaufman S J Pediatr; 1986 Oct; 109(4):572-8. PubMed ID: 3489828 [No Abstract] [Full Text] [Related]
18. [Development of the biosynthesis and excretion of pterins in phenylketonuria and its variants]. Curtius HC; Niederwieser A Arch Fr Pediatr; 1983; 40 Suppl 1():227-30. PubMed ID: 6349572 [No Abstract] [Full Text] [Related]
20. Development of a model for assessment of phenylalanine hydroxylase activity in newborns with phenylketonuria receiving tetrahydrobiopterin: a potential for practical implementation. Bik-Multanowski M; Pietrzyk JJ; Didycz B; Szymczakiewicz-Multanowska A Mol Genet Metab; 2008 Jul; 94(3):389-90. PubMed ID: 18482855 [No Abstract] [Full Text] [Related] [Next] [New Search]