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Nutrients|August 26, 2023
Phenylalanine Tolerance over Time in Phenylketonuria: A Systematic Review and Meta-AnalysisAlex Pinto, Fatma Ilgaz, Sharon Evans, et al.Nutrients|September 6, 2019
Long-Term Growth in Phenylketonuria: A Systematic Review and Meta-AnalysisFatma Ilgaz, Alex Pinto, Hülya Gökmen-Özel, et al.Molecular Genetics and Metabolism Reports|June 7, 2021
Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliaseJúlio César Rocha, Heather Bausell, Amaya Bélanger-Quintana, et al.Orphanet Journal of Rare Diseases|April 5, 2020
Dried blood spot versus venous blood sampling for phenylalanine and tyrosineKimber van Vliet, Wiggert G van Ginkel, Esther van Dam, et al.Nutrients|July 1, 2020
Aspartame and Phe-Containing Degradation Products in Soft Drinks across EuropeKimber van Vliet, Elise S Melis, Pim de Blaauw, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|May 22, 2019
A series of three case reports in patients with phenylketonuria performing regular exercise: first steps in dietary adjustmentJúlio César Rocha, Esther van Dam, Kirsten Ahring, et al.Journal of Inherited Metabolic Disease|September 11, 2019
The first European guidelines on phenylketonuria: Usefulness and implications for BH<sub>4</sub> responsiveness testingRoeland A F Evers, Annemiek M J van Wegberg, Karen Anjema, et al.Molecular Genetics and Metabolism|January 12, 2020
Does the 48-hour BH4 loading test miss responsive PKU patients?Annemiek M J van Wegberg, Roeland A F Evers, Esther van Dam, et al.JIMD Reports|January 26, 2017
What Is the Best Blood Sampling Time for Metabolic Control of Phenylalanine and Tyrosine Concentrations in Tyrosinemia Type 1 Patients?Esther van Dam, Anne Daly, Gineke Venema-Liefaard, et al.Annals of Nutrition & Metabolism|November 25, 2015
Weight Management in Phenylketonuria: What Should Be MonitoredJulio César Rocha, Margreet van Rijn, Esther van Dam, et al.Pageof 2