Niederwieser A - Search Results

1

Tetrahydrobiopterin biosynthesis. Studies with specifically labeled (2H)NAD(P)H and 2H2O and of the enzymes involved.

Curtius HC, Heintel D, Ghisla S, Kuster T, Leimbacher W, Niederwieser A. Curtius HC, et al. Among authors: niederwieser a. Eur J Biochem. 1985 May 2;148(3):413-9. doi: 10.1111/j.1432-1033.1985.tb08855.x. Eur J Biochem. 1985. PMID: 3888618 Free article.

2

Biosynthesis of tetrahydrobiopterin in man.

Curtius HC, Heintel D, Ghisla S, Kuster T, Leimbacher W, Niederwieser A. Curtius HC, et al. Among authors: niederwieser a. J Inherit Metab Dis. 1985;8 Suppl 1:28-33. doi: 10.1007/BF01800656. J Inherit Metab Dis. 1985. PMID: 3930838 Review.

3

Atypical phenylketonuria with "dihydrobiopterin synthetase" deficiency: absence of phosphate-eliminating enzyme activity demonstrated in liver.

Niederwieser A, Leimbacher W, Curtius HC, Ponzone A, Rey F, Leupold D. Niederwieser A, et al. Eur J Pediatr. 1985 May;144(1):13-6. doi: 10.1007/BF00491917. Eur J Pediatr. 1985. PMID: 2990933

4

Tetrahydrobiopterin deficiency: assay for 6-pyruvoyl-tetrahydropterin synthase activity in erythrocytes, and detection of patients and heterozygous carriers.

Shintaku H, Niederwieser A, Leimbacher W, Curtius HC. Shintaku H, et al. Among authors: niederwieser a. Eur J Pediatr. 1988 Jan;147(1):15-9. doi: 10.1007/BF00442604. Eur J Pediatr. 1988. PMID: 3276524

5

"Peripheral" tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosity.

Niederwieser A, Shintaku H, Leimbacher W, Curtius HC, Hyànek J, Zeman J, Endres W. Niederwieser A, et al. Eur J Pediatr. 1987 May;146(3):228-32. doi: 10.1007/BF00716465. Eur J Pediatr. 1987. PMID: 3297709

6

Biosynthesis and metabolism of pterins in peripheral blood mononuclear cells and leukemia lines of man and mouse.

Schoedon G, Troppmair J, Fontana A, Huber C, Curtius HC, Niederwieser A. Schoedon G, et al. Among authors: niederwieser a. Eur J Biochem. 1987 Jul 15;166(2):303-10. doi: 10.1111/j.1432-1033.1987.tb13515.x. Eur J Biochem. 1987. PMID: 3301338 Free article.

7

Tetrahydrobiopterin biosynthetic pathway and deficiency.

Niederwieser A, Curtius HC. Niederwieser A, et al. Enzyme. 1987;38(1-4):302-11. doi: 10.1159/000469220. Enzyme. 1987. PMID: 3326735 Review.

8

Differential diagnosis of tetrahydrobiopterin deficiency.

Niederwieser A, Ponzone A, Curtius HC. Niederwieser A, et al. J Inherit Metab Dis. 1985;8 Suppl 1:34-8. doi: 10.1007/BF01800657. J Inherit Metab Dis. 1985. PMID: 3930839

9

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

Niederwieser A, Curtius HC, Wang M, Leupold D. Niederwieser A, et al. Eur J Pediatr. 1982 Mar;138(2):110-2. doi: 10.1007/BF00441135. Eur J Pediatr. 1982. PMID: 7094929

10

Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuria.

Niederwieser A, Shintaku H, Hasler T, Curtius HC, Lehmann H, Guardamagna O, Schmidt H. Niederwieser A, et al. Eur J Pediatr. 1986 Aug;145(3):176-8. doi: 10.1007/BF00446058. Eur J Pediatr. 1986. PMID: 3533549

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