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Acta Paediatrica Scandinavica|May 1, 1977
On indications for treatment of the hyperphenylalaninemic neonateF Güttler, E WambergAnnals of Clinical Biochemistry|May 1, 1977
Different phenotypes for phenylalanine hydroxylase deficiencyF Güttler, G HansenActa Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemiaF Güttler, P GuldbergJournal of Inherited Metabolic Disease|January 1, 1986
Dietary problems of phenylketonuria: effect on CNS transmitters and their possible role in behaviour and neuropsychological functionF Güttler, H LouScandinavian Journal of Clinical and Laboratory Investigation|December 1, 1977
Serum tyrosine within the first hour after an oral load of phenylalanineF Güttler, G HansenEuropean Journal of Pediatrics|July 1, 1996
The influence of mutations of enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiencyF Güttler, P GuldbergJournal of Cell Science|June 1, 1979
Arrest of cell membrane movements by in vitro incubation with polycation reversed by polyanionP Ebbesen, F GüttlerEuropean Journal of Pediatrics|October 24, 2000
Mutation analysis anticipates dietary requirements in phenylketonuriaF Güttler, P GuldbergActa Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: methods for their characterizationP Guldberg, F GüttlerPageof 53