Results 131 to 140 of about 16,591 (243)

Nutritional Status and Physical Activity Levels in Adult Patients with Phenylketonuria. [PDF]

open access: yesNutrients
Kalkan D   +6 more
europepmc   +1 more source

LNAA supplementation in a PKU mouse model.

open access: yes, 2013
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  

Restricted eating behavior in children with PKU and HPA

open access: yes, 2012
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]

open access: yesHealth Sci Rep
Ilkhanipoor H   +5 more
europepmc   +1 more source

PKU [PDF]

open access: yes, 2019
openaire   +1 more source

Body composition in adults with phenylketonuria: A 5 years follow-up study. [PDF]

open access: yesMol Genet Metab Rep
Franceschetto BF   +7 more
europepmc   +1 more source

Impact of depression on quality of life in PKU children. [PDF]

open access: yesEur J Pediatr
Abuelela IS   +4 more
europepmc   +1 more source

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