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1. [Genotyping and treatment modification in patients with phenylketonuria: an introduction to pharmacogenomics].
2. [Maternal phenylketonuria: dietary treatment of a 2 generation illness].
3. Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency.
4. The impact of metabolic control on cognition, neurophysiology, and well-being in PKU: A systematic review and meta-analysis of the within-participant literature.
5. 5-year retrospective analysis of patients with phenylketonuria (PKU) and hyperphenylalaninemia treated at two specialized clinics.
6. Metabolomics for improved treatment monitoring of phenylketonuria: urinary biomarkers for non-invasive assessment of dietary adherence and nutritional deficiencies.
7. Vitamin Status in Patients with Phenylketonuria: A Systematic Review and Meta-Analysis.
8. Bone mineral density is within normal range in most adult phenylketonuria patients.
9. [Treatment of phenylketonuria: wish and reality].
10. Health status and comorbidities of adult patients with phenylketonuria (PKU) in France with a focus on early-diagnosed patients - A nationwide study of health insurance claims data.