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14 in total

1. Hyperphenylalaninaemia due to dihydropteridine reductase deficiency.

Authors: H Gröbe; K Bartholome; S Milstien; S Kaufman
Journal: Eur J Pediatr Date: 1978-09-08 Impact factor: 3.183

Review 2. Atypical cases of phenylketonuria.

Authors: J L Dhondt; J P Farriaux
Journal: Eur J Pediatr Date: 1987 Impact factor: 3.183

3. Blood spots on Guthrie cards can be used for inherited tetrahydrobiopterin deficiency screening in hyperphenylalaninaemic infants.

Authors: R J Leeming; P A Barford; J A Blair; I Smith
Journal: Arch Dis Child Date: 1984-01 Impact factor: 3.791

4. Hyperphenylalaninemia due to impaired dihydrobiopterin biosynthesis.

Authors: T Tanaka; K Aihara; K Iwai; M Kohashi; K Tomita; K Narisawa; N Arai; H Yoshida; T Usui
Journal: Eur J Pediatr Date: 1981-07 Impact factor: 3.183

5. Diagnosis of malignant hyperphenylalaninaemia.

Authors: D M Danks; R G Cotton; P Schlesinger
Journal: Arch Dis Child Date: 1979-05 Impact factor: 3.791

6. Biopterin derivatives in normal and phenylketonuric patients after oral loads of L-phenylalanine, L-tyrosine, and L-tryptophan.

Authors: R J Leeming; J A Blair; A Green; D N Raine
Journal: Arch Dis Child Date: 1976-10 Impact factor: 3.791

7. 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: L-dopa and 5-hydroxytryptophan therapy in phenylketonuria with normal phenylalanine-hydroxylase activity.