Pages that link to "Q70375635"

The following pages link to Preliminary report on the effects of diet discontinuation in PKU (Q70375635):

Displaying 24 items.

• Dietary interventions for phenylketonuria (Q24240788) (← links)
• Biological and social influences on cognitive control processes dependent on prefrontal cortex (Q29397599) (← links)
• Dietary interventions for phenylketonuria. (Q33909733) (← links)
• Biochemical and neuropsychological effects of elevated plasma phenylalanine in patients with treated phenylketonuria. A model for the study of phenylalanine and brain function in man (Q34521900) (← links)
• Effect on intelligence of relaxing the low phenylalanine diet in phenylketonuria (Q35626272) (← links)
• Protective effect of recombinant adeno-associated virus 2/8-mediated gene therapy from the maternal hyperphenylalaninemia in offsprings of a mouse model of phenylketonuria (Q36966120) (← links)
• Predictability and inconsistencies in the cognitive outcome of early treated PKU patients (Q38610970) (← links)
• Maternal phenylketonuria (PKU)--a review (Q39669102) (← links)
• Recombinant DNA Probes Used to Detect Genetic Disorders of the Liver (Q40076802) (← links)
• Barriers to successful dietary control among pregnant women with phenylketonuria (Q40655265) (← links)
• Cognitive deficits in a genetic mouse model of the most common biochemical cause of human mental retardation. (Q45355314) (← links)
• Phenylketonuric patients decades after diet. (Q52021152) (← links)
• Decreased vigilance and neurotransmitter synthesis after discontinuation of dietary treatment for phenylketonuria in adolescents. (Q52083180) (← links)
• Paired comparisons between early treated PKU children and their matched sibling controls on intelligence and school achievement test results at eight years of age. (Q52698622) (← links)
• Reinstitution of diet therapy in PKU patients from twenty-two US clinics. (Q52948854) (← links)
• Maternal PKU: control of an emerging problem. (Q53847684) (← links)
• Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria (Q55062488) (← links)
• Behavior disturbance in 8-year-old children with early treated phenylketonuria (Q56609578) (← links)
• Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine (Q59549032) (← links)
• The effects of diet discontinuation in children with phenylketonuria (Q69468087) (← links)
• Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria (Q70566130) (← links)
• Diet policies of PKU clinics in the United States (Q71316626) (← links)
• Phenylketonuria: treatment in adolescence and adult life (Q71583673) (← links)
• Norwalk virus: a major cause of epidemic gastroenteritis (Q72962938) (← links)