Neuropsychiatric Function Improvement in Pediatric Patients With Phenylketonuria.
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[1] S. Waisbren,et al. Improved attention linked to sustained phenylalanine reduction in adults with early‐treated phenylketonuria , 2021, American journal of medical genetics. Part A.
[2] S. Christ,et al. Inter- and intra-tract analysis of white matter abnormalities in individuals with early-treated phenylketonuria (PKU). , 2020, Molecular genetics and metabolism.
[3] F. Spronsen,et al. Tetrahydrobiopterin treatment in phenylketonuria: A repurposing approach , 2020, Journal of inherited metabolic disease.
[4] M. Walterfang,et al. Psychiatric and Cognitive Aspects of Phenylketonuria: The Limitations of Diet and Promise of New Treatments , 2019, Front. Psychiatry.
[5] I. Schwartz,et al. Attention-deficit hyperactivity disorder in Brazilian patients with phenylketonuria , 2018, Acta Neurologica Belgica.
[6] C. Hollak,et al. Long-Term Follow-Up of Cognition and Mental Health in Adult Phenylketonuria: A PKU-COBESO Study , 2017, Behavior Genetics.
[7] T. van Amelsvoort,et al. Cerebral dopamine deficiency, plasma monoamine alterations and neurocognitive deficits in adults with phenylketonuria , 2017, Psychological Medicine.
[8] D. Bilder,et al. Neuropsychiatric comorbidities in adults with phenylketonuria: A retrospective cohort study. , 2017, Molecular genetics and metabolism.
[9] S. Cederbaum,et al. Adherence to clinic recommendations among patients with phenylketonuria in the United States. , 2017, Molecular genetics and metabolism.
[10] U. Lichter-Konecki,et al. Phenylketonuria (PKU): A problem solved? , 2015, Molecular genetics and metabolism reports.
[11] S. Stahl,et al. A randomized, placebo-controlled, double-blind study of sapropterin to treat ADHD symptoms and executive function impairment in children and adults with sapropterin-responsive phenylketonuria. , 2015, Molecular genetics and metabolism.
[12] D. Elbourne,et al. Systematic review of the Hawthorne effect: New concepts are needed to study research participation effects☆ , 2014, Journal of clinical epidemiology.
[13] John J. Mitchell,et al. Phenylalanine hydroxylase deficiency: diagnosis and management guideline , 2013, Genetics in Medicine.
[14] Amanda J. Moffitt,et al. The effects of tetrahydrobiopterin (BH4) treatment on brain function in individuals with phenylketonuria☆ , 2013, NeuroImage: Clinical.
[15] P. Fernhoff,et al. Safety of extended treatment with sapropterin dihydrochloride in patients with phenylketonuria: results of a phase 3b study. , 2011, Molecular genetics and metabolism.
[16] John J. Mitchell,et al. Phenylalanine hydroxylase deficiency , 2011, Genetics in Medicine.
[17] Larissa V Furtado,et al. Correlation of age-specific phenylalanine levels with intellectual outcome in patients with phenylketonuria , 2011, Journal of Inherited Metabolic Disease.
[18] B. Burton,et al. Tetrahydrobiopterin therapy for phenylketonuria in infants and young children. , 2011, The Journal of pediatrics.
[19] R. Carpenter,et al. Dietary treatment of phenylketonuria: the effect of phenylalanine on reaction time , 2011, Journal of Inherited Metabolic Disease.
[20] G. Enns,et al. Suboptimal outcomes in patients with PKU treated early with diet alone: revisiting the evidence. , 2010, Molecular genetics and metabolism.
[21] J. Vockley,et al. Efficacy of sapropterin dihydrochloride in increasing phenylalanine tolerance in children with phenylketonuria: a phase III, randomized, double-blind, placebo-controlled study. , 2009, The Journal of pediatrics.
[22] S. Cederbaum,et al. The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study , 2007, Journal of Inherited Metabolic Disease.
[23] S. Wood,et al. Are Neuropsychological Impairments in Children with Early-Treated Phenylketonuria (PKU) Related to White Matter Abnormalities or Elevated Phenylalanine Levels? , 2007, Developmental neuropsychology.
[24] S. Waisbren,et al. Phenylalanine blood levels and clinical outcomes in phenylketonuria: a systematic literature review and meta-analysis. , 2007, Molecular genetics and metabolism.
[25] A. Chakrapani,et al. Efficacy of sapropterin dihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III randomised placebo-controlled study , 2007, The Lancet.
[26] S. Packman,et al. Executive functioning in children and adolescents with phenylketonuria , 2007, Clinical genetics.
[27] A. Fox,et al. Meta-Analysis of Neuropsychological Symptoms of Adolescents and Adults with PKU , 2007, Neuropsychology Review.
[28] R. Artuch,et al. School performance in early and continuously treated phenylketonuria. , 2005, Pediatric neurology.
[29] R. Artuch,et al. Cognitive functions in classic phenylketonuria and mild hyperphenylalaninaemia: experience in a paediatric population. , 2005, Developmental medicine and child neurology.
[30] C. Vladutiu,et al. Prevalence of stimulant use for attentional dysfunction in children with phenylketonuria , 2004, Journal of Inherited Metabolic Disease.
[31] G. Levi,et al. Executive function impairment in early-treated PKU subjects with normal mental development , 2004, Journal of Inherited Metabolic Disease.
[32] S. Waisbren,et al. Timing is everything: executive functions in children exposed to elevated levels of phenylalanine. , 2003, Neuropsychology.
[33] J. Sergeant,et al. Sustained attention and inhibition of cognitive interference in treated phenylketonuria: associations with concurrent and lifetime phenylalanine concentrations , 2002, Neuropsychologia.
[34] J. Sergeant,et al. Inhibition of Prepotent Responding and Attentional Flexibility in Treated Phenylketonuria , 2002, Developmental neuropsychology.
[35] A. Boneh,et al. How practical are recommendations for dietary control in phenylketonuria? , 2002, The Lancet.
[36] Robert Reid,et al. Parent Ratings of Attention-Deficit/Hyperactivity Disorder Symptoms: Factor Structure and Normative Data , 1998 .
[37] J. Jenkins,et al. Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter change. , 1995, The Journal of pediatrics.
[38] A. Rupp,et al. Sustained attention in adult phenylketonuria: the influence of the concurrent phenylalanine-blood-level. , 1994, Journal of clinical and experimental neuropsychology.
[39] D. Clark,et al. Reliability and validity of the Hamilton Anxiety Rating Scale in an adolescent sample. , 1994, Journal of the American Academy of Child and Adolescent Psychiatry.
[40] M. Hamilton,et al. Development of a rating scale for primary depressive illness. , 1967, The British journal of social and clinical psychology.
[41] M. Hamilton. A RATING SCALE FOR DEPRESSION , 1960, Journal of neurology, neurosurgery, and psychiatry.
[42] M. Hamilton. The assessment of anxiety states by rating. , 1959, The British journal of medical psychology.
[43] Mayara Thays Beckhauser,et al. Attention Deficit Disorder with Hyperactivity Symptoms in Early-Treated Phenylketonuria Patients , 2020, Iranian journal of child neurology.
[44] K. Wyrwich,et al. Content Validity of the ADHD Rating Scale (ADHD RS-IV) and Adult ADHD Self-Report Scale (ASRS) in Phenylketonuria: , 2016 .
[45] H. Coon,et al. A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics. , 2013, Molecular genetics and metabolism.
[46] P. Anderson,et al. White matter pathology in phenylketonuria. , 2010, Molecular genetics and metabolism.
[47] S. Christ,et al. Executive function in early-treated phenylketonuria: profile and underlying mechanisms. , 2010, Molecular genetics and metabolism.
[48] I. Heuser,et al. The Hamilton Anxiety Scale: reliability, validity and sensitivity to change in anxiety and depressive disorders. , 1988, Journal of affective disorders.
[49] D. Freides,et al. 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. , 1985, The Journal of clinical investigation.