Nutritional Status and Physical Activity Levels in Adult Patients with Phenylketonuria. [PDF]
Kalkan D +6 more
europepmc +1 more source
LNAA supplementation in a PKU mouse model.
Phenylketonuria (PKU) is an inborn error of metabolism in which the amino acid phenylalanine (Phe) cannot be converted to tyrosine. Untreated, the markedly elevated blood Phe concentrations lead to severe mental retardation and psychiatric problems.
Vliet, D. van (Danique)
core
Nutritional and Therapeutic Strategies in Paediatric Phenylketonuria: A Narrative Literature Review. [PDF]
Jones H, Strehle EM.
europepmc +1 more source
Restricted eating behavior in children with PKU and HPA
Thesis (Master's)--University of Washington, 2012Phenylketonuria (PKU) and hyperphenylalaninemia (HPA) are two genetic disorders that affect the metabolism of the amino acid phenylalanine (Phe), leading to increased serum Phe concentrations, and possible
Bailey, Sarah
core
Oral Health Status of Children and Adolescents With Phenylketonuria: A Case-Control Study. [PDF]
Ilkhanipoor H +5 more
europepmc +1 more source
Inert Catalytic Sites Unlocked by Micropollutants for Rapid Water Decontamination with Near-Complete Chemical Utilization. [PDF]
Li YH +7 more
europepmc +1 more source
Body composition in adults with phenylketonuria: A 5 years follow-up study. [PDF]
Franceschetto BF +7 more
europepmc +1 more source
Impact of depression on quality of life in PKU children. [PDF]
Abuelela IS +4 more
europepmc +1 more source
Changes in Child Behaviour Following a Brief Parenting Intervention (Triple P) for Families of Children with Phenylketonuria (PKU): A Case Series. [PDF]
Kirby G +5 more
europepmc +1 more source

