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22 in total

1. Malignant hyperphenylalaninaemia--current status (June 1977).

Authors: D M Danks; K Bartholomé; B E Clayton; H Curtius; H Gröbe; S Kaufman; R Leeming; W Pfleiderer; H Rembold; F Rey
Journal: J Inherit Metab Dis Date: 1978 Impact factor: 4.982

2. Tetrahydrobiopterin non-responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant protein.

Authors: R G Cotton; I Jennings; G Bracco; A Ponzone; O Guardamagna
Journal: J Inherit Metab Dis Date: 1986 Impact factor: 4.982

3. Direct binding of GTP cyclohydrolase and tyrosine hydroxylase: regulatory interactions between key enzymes in dopamine biosynthesis.

Authors: Kevin M Bowling; Zhinong Huang; Dong Xu; Faiza Ferdousy; Christopher D Funderburk; Nirmala Karnik; Wendi Neckameyer; Janis M O'Donnell
Journal: J Biol Chem Date: 2008-09-18 Impact factor: 5.157

10. Atypical phenylketonuria with defective biopterin metabolism. Monotherapy with tetrahydrobiopterin or sepiapterin, screening and study of biosynthesis in man.

Authors: A Niederwieser; H C Curtius; M Wang; D Leupold
Journal: Eur J Pediatr Date: 1982-03 Impact factor: 3.183

Letter: Tetrahydrobiopterin treatment of variant form of phenylketonuria.

1. Malignant hyperphenylalaninaemia--current status (June 1977).

2. Tetrahydrobiopterin non-responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant protein.

3. Direct binding of GTP cyclohydrolase and tyrosine hydroxylase: regulatory interactions between key enzymes in dopamine biosynthesis.

4. A model for hyperphenylalaninaemia due to tetrahydrobiopterin deficiency.

5. Renal balance of pterin cofactors in the rat. A clearance and micropuncture study.

6. Hyperphenylalaninemia due to impaired dihydrobiopterin biosynthesis.

7. The role of tetrahydrofolate dehydrogenase in the hepatic supply of tetrahydrobiopterin in rats.

8. Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading test.

9. Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4.

10. Atypical phenylketonuria with defective biopterin metabolism. Monotherapy with tetrahydrobiopterin or sepiapterin, screening and study of biosynthesis in man.