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Are Neuropsychological Impairments in Children with Early-Treated Phenylketonuria (PKU) Related to White Matter Abnormalities or Elevated Phenylalanine Levels?

https://doi.org/10.1080/87565640701375963

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Outgoing claims: the papers this work cites, builds on, or argues with.

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White matter abnormalities in patients with treated hyperphenylalaninaemia: Magnetic resonance relaxometry and proton spectroscopy findings

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Disturbed myelination in patients with treated hyperphenylalaninaemia: evaluation with magnetic resonance imaging

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Attentional and executive impairments in children with spastic cerebral palsy

inferred← citeshttps://doi.org/10.1111/j.1469-8749.2010.03869.xopenalex-snapshot

Neurocognitive function in mild hyperphenylalaninemia

inferred← citeshttps://doi.org/10.1111/jnc.12683openalex-snapshot

Altered brain protein expression profiles are associated with molecular neurological dysfunction in the PKU mouse model

inferred← citeshttps://doi.org/10.1111/mono.12036openalex-snapshot

VI. NIH TOOLBOX COGNITION BATTERY (CB): MEASURING PROCESSING SPEED

inferred← citeshttps://doi.org/10.1139/bcb-2013-0023openalex-snapshot

DNA damage induced by phenylalanine and its analogue p-chlorophenylalanine in blood and brain of rats subjected to a model of hyperphenylalaninemia

inferred← citeshttps://doi.org/10.1159/000312815openalex-snapshot

Neuropsychological Functioning in Early-Treated Phenylketonuria – A Review

inferred← citeshttps://doi.org/10.1159/000320531openalex-snapshot

Función neuropsicológica en la fenilcetonuria tratada precozmente: Una revisión

inferred← citeshttps://doi.org/10.1159/000323169openalex-snapshot

Altérations neuropsychologiques chez les patients phénylcétonuriques traités précocement: Revue

inferred← citeshttps://doi.org/10.1172/jci184299openalex-snapshot

GluN2B suppression restores phenylalanine-induced neuroplasticity and cognition impairments in a mouse model of phenylketonuria

inferred← citeshttps://doi.org/10.1177/0883073812442589openalex-snapshot

Pilot Study on Executive Function and Adaptive Skills in Adolescents and Young Adults With Mitochondrial Disease

inferred← citeshttps://doi.org/10.1186/1750-1172-8-133openalex-snapshot

Phenylketonuria: reduced tyrosine brain influx relates to reduced cerebral protein synthesis

inferred← citeshttps://doi.org/10.1186/s11689-025-09622-8openalex-snapshot

Diffusivity alterations related to cognitive performance and phenylalanine levels in early-treated adults with phenylketonuria

inferred← citeshttps://doi.org/10.1186/s13023-018-0839-xopenalex-snapshot

Status of nutrients important in brain function in phenylketonuria: a systematic review and meta-analysis

inferred← citeshttps://doi.org/10.1186/s13023-018-0912-5openalex-snapshot

White matter microstructural damage in early treated phenylketonuric patients

inferred← citeshttps://doi.org/10.1186/s13023-019-1225-zopenalex-snapshot

Adult cognitive outcomes in phenylketonuria: explaining causes of variability beyond average Phe levels

inferred← citeshttps://doi.org/10.1186/s13023-025-03824-yopenalex-snapshot

Factors associated with psycho-behavioral problems among 100 children with phenylketonuria aged 6–18 years

inferred← citeshttps://doi.org/10.12659/msm.909146openalex-snapshot

Behavioral and Emotional Problems in Early-Treated Brazilian Children and Adolescents with Phenylketonuria

inferred← citeshttps://doi.org/10.1515/jpem-2013-0425openalex-snapshot

Adult human liver mesenchymal progenitor cells express phenylalanine hydroxylase

inferred← citeshttps://doi.org/10.1542/peds.2011-1715openalex-snapshot

Neurocognitive Phenotype of Isolated Methylmalonic Acidemia

inferred← citeshttps://doi.org/10.1542/peds.2011-1715dopenalex-snapshot

Neurocognitive Phenotype of Isolated Methylmalonic Acidemia

inferred← citeshttps://doi.org/10.1590/1982-0216201515313openalex-snapshot

Fenilcetonúria e habilidades de leitura e escrita

inferred← citeshttps://doi.org/10.1590/s0104-56872010000300031openalex-snapshot

Desempenho de crianças com fenilcetonúria no Teste de Screening de Desenvolvimento Denver - II

inferred← citeshttps://doi.org/10.1590/s1516-18462009005000055openalex-snapshot

Desenvolvimento infantil na fenilcetonúria: atuação fonoaudiológica

inferred← citeshttps://doi.org/10.1590/s1516-18462010000100019openalex-snapshot

Alterações auditivas e fenilcetonúria: uma revisão sistemática

inferred← citeshttps://doi.org/10.1590/s1516-80342010000300012openalex-snapshot

Achados audiológicos em crianças com fenilcetonúria

inferred← citeshttps://doi.org/10.1590/s1678-77572009000700012openalex-snapshot

Communicative and psycholinguistic abilities in children with phenylketonuria and congenital hypothyroidism

inferred← citeshttps://doi.org/10.1684/nrp.2018.0470openalex-snapshot

L’hypothèse dysexécutive chez l’enfant atteint de phénylcétonurie : revue de littérature et prospective de recherche

inferred← citeshttps://doi.org/10.17151/biosa.2018.17.1.6openalex-snapshot

Deficiencia de fenilalanina hidroxilasa : espectro clínico y estado actual del diagnóstico en Colombia.

inferred← citeshttps://doi.org/10.20517/jtgg.2020.09openalex-snapshot

Novel imaging technologies for genetic diagnoses in the inborn errors of metabolism

inferred← citeshttps://doi.org/10.2139/ssrn.5376978openalex-snapshot

Intellectual Profiles in Children with Unilateral and Bilateral Cerebral Palsy: a Multilevel Analysis of the Wisc-Iv Scale

inferred← citeshttps://doi.org/10.2147/ndt.s176198openalex-snapshot

Clinical and neuropsychological outcomes for children with phenylketonuria in Upper Egypt; a single-center study over 5 years

inferred← citeshttps://doi.org/10.2196/63644openalex-snapshot

Leveraging Cognitive and Speech Ecological Momentary Assessment in Individuals With Phenylketonuria: Development and Usability Study of Cognitive Fluctuations in a Rare Disease Population

inferred← citeshttps://doi.org/10.2478/jomb-2013-0046openalex-snapshot

Association of Mitochondrial DNA Variants and Cognitive Impairment of Phenylketonuria Patients / POVEZANOST VARIJANTI U MITOHONDRIJALNOJ DNK I KOGNITIVNOG FENOTIPA KOD PACIJENATA SA FENILKETONURIJOM

inferred← citeshttps://doi.org/10.24953/turkjped.2018.06.001openalex-snapshot

Cognitive and behavioral impairment in mild hyperphenylalaninemia

inferred← citeshttps://doi.org/10.3109/08880018.2010.503340openalex-snapshot

LANGUAGE SKILLS IN A CHILD WITH LEBER HEREDITARY OPTIC NEUROPATHY FOLLOWING INTRATHECAL CHEMOTHERAPY FOR ACUTE LYMPHOBLASTIC LEUKEMIA

inferred← citeshttps://doi.org/10.32469/10355/94051openalex-snapshot

The role of anxiety in the relationship between Phenylketonuria and working memory

inferred← citeshttps://doi.org/10.33588/rn.5504.2012038openalex-snapshot

Evolución neurológica, neuropsicológica y oftalmológica tras un año de suplementación con ácido docosahexaenoico en pacientes fenilcetonúricos

inferred← citeshttps://doi.org/10.33612/diss.135584531openalex-snapshot

Tetrahydrobiopterin in phenylketonuria: Who can benefit?

inferred← citeshttps://doi.org/10.3389/fped.2021.603126openalex-snapshot

Measurement of Cognition for the National Children's Study

inferred← citeshttps://doi.org/10.3389/fpsyt.2019.00561openalex-snapshot

Psychiatric and Cognitive Aspects of Phenylketonuria: The Limitations of Diet and Promise of New Treatments

inferred← citeshttps://doi.org/10.3390/jcm11041061openalex-snapshot

The Utility of Genomic Testing for Hyperphenylalaninemia

inferred← citeshttps://doi.org/10.3390/sym14020345openalex-snapshot

From Hemispheric Asymmetry through Sensorimotor Experiences to Cognitive Outcomes in Children with Cerebral Palsy

inferred← citeshttps://doi.org/10.34719/vtew6097openalex-snapshot

Living With Pku: The Lived Experience Of Irish Adults With Early Diagnosed Phenylketonuria On Long Term Dietary Therapy

inferred← citeshttps://doi.org/10.37099/mtu.dc.etds/193openalex-snapshot

Inhibition of L-type amino acid transport with non-physiological amino acids in the Pahenu2 mouse model of phenylketonuria

inferred← citeshttps://doi.org/10.37897/rjp.2013.1.1openalex-snapshot

INFLUENŢA DIETEI FĂRĂ FENILALANINĂ ASUPRA DEZVOLTĂRII NEUROPSIHICE ÎN FENILCETONURIE

inferred← citeshttps://doi.org/10.3917/lcp.250.0030openalex-snapshot

Une recherche-action autour du processus d’annonce de la phénylcétonurie : entre dispositif de santé publique et retentissements psychiques

inferred← citeshttps://doi.org/10.4103/mjbl.mjbl_1133_23openalex-snapshot

Total Head Growth in Patients with Phenylketonuria Diagnosed by Newborn Screening Test

inferred← citeshttps://doi.org/10.5937/medi0-64781openalex-snapshot

Phenylketonuria: Importance of neonatal screening, insights into genotype-phenotype correlations, and novel therapeutic approaches

inferred← citeshttps://doi.org/10.7936/k7h41pd9openalex-snapshot

Phenylalanine Control Predicts Cognition and White Matter Integrity in Children with Phenylketonuria

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