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Helvetica Paediatrica Acta|February 1, 1978
In vivo studies of the phenylalanine-4-hydroxylase system in hyperphenylalaninemics and phenylketonuricsH C Curtius, M J Zagalak, K Baerlocher, et al.European Journal of Biochemistry|November 1, 1996
Location of the active site and proposed catalytic mechanism of pterin-4a-carbinolamine dehydrataseS Köster, G Stier, R Ficner, et al.Journal of Inherited Metabolic Disease|January 1, 1996
International database of tetrahydrobiopterin deficienciesN Blau, I Barnes, J L DhondtEuropean Journal of Pediatrics|August 1, 1986
Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuriaA Niederwieser, H Shintaku, T Hasler, et al.European Journal of Pediatrics|May 1, 1987
"Peripheral" tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosityA Niederwieser, H Shintaku, W Leimbacher, et al.Lancet (London, England)|January 20, 1979
Atypical phenylketonuria caused by 7, 8-dihydrobiopterin synthetase deficiencyA Niederwieser, H C Curtius, O Bettoni, et al.Catheterization and Cardiovascular Diagnosis|January 1, 1977
Coronary artery fistula: estimation of shunt using 99m Tc-albumin particlesN Blau, M H Adatepe, F R BeggLijecnicki Vjesnik|July 1, 1994
[Homocystinuria: case reports with a note on hyperhomocysteinemia as a risk factor for the early onset of vascular disease]I Barić, N Barisić, N Blau, et al.The Turkish Journal of Pediatrics|January 1, 1996
Tetrahydrobiopterin and inherited hyperphenylalaninemiasN Blau, B Thony, M Spada, et al.Clinical Chemistry|December 10, 1999
Single-step mutation scanning of the 6-pyruvoyltetrahydropterin synthase gene in patients with hyperphenylalaninemiaA Romstad, P Guldberg, N Blau, et al.Pageof 21