Esther van Dam

University Medical Center Groningen — Netherlands

Biochemistry, Genetics and Molecular Biology · Life Sciences

17h-index877citations40works2.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Metabolism and Genetic Disorders(30), Diet and metabolism studies(23), Mitochondrial Function and Pathology(9), Neonatal Health and Biochemistry(5), Amino Acid Enzymes and Metabolism(5)

Publications37 total

Multicenter study on long-term growth in patients with phenylketonuria
Orphanet Journal of Rare Diseases·2025Open Access
Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria Severity
Nutrients·2024· 1 citedOpen Access
Blood Phenylalanine Levels in Patients with Phenylketonuria from Europe between 2012 and 2018: Is It a Changing Landscape?
Nutrients·2024· 9 citedOpen Access
P.28 Blood phenylalanine control in patients with phenylketonuria in Europe: is it a changing landscape?
Molecular Genetics and Metabolism·2024
Phenylalanine Tolerance over Time in Phenylketonuria: A Systematic Review and Meta-Analysis
Nutrients·2023· 15 citedOpen Access
Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase
Molecular Genetics and Metabolism Reports·2021· 23 citedOpen Access
A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single‐center study and the generation of www.emergencyprotocol.net
Journal of Inherited Metabolic Disease·2021· 23 citedOpen Access
Effect of BH4 on blood phenylalanine and tyrosine variations in patients with phenylketonuria
Molecular Genetics and Metabolism·2021· 11 citedOpen Access
Aspartame and Phe-Containing Degradation Products in Soft Drinks across Europe
Nutrients·2020· 16 citedOpen Access
Dried blood spot versus venous blood sampling for phenylalanine and tyrosine
Orphanet Journal of Rare Diseases·2020· 34 citedOpen Access
Sugar-Induced Obesity and Insulin Resistance Are Uncoupled from Shortened Survival in Drosophila
Cell Metabolism·2020· 135 citedOpen Access
Dried blood spot versus venous blood sampling for phenylalanine and tyrosine
Research Square (Research Square)·2020Open Access
A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: a retrospective, single-center chart review of 128 patients
Research Square (Research Square)·2020· 1 citedOpen Access
Does the 48-hour BH4 loading test miss responsive PKU patients?
Molecular Genetics and Metabolism·2019· 10 citedOpen Access
Dietary practices in methylmalonic acidaemia: a European survey
Journal of Pediatric Endocrinology and Metabolism·2019· 10 citedOpen Access
Dried blood spot versus venous blood sampling for phenylalanine and tyrosine: a large difference?
2019Open Access
The first European guidelines on phenylketonuria: Usefulness and implications for BH<sub>4</sub> responsiveness testing
Journal of Inherited Metabolic Disease·2019· 18 citedOpen Access
Long-Term Growth in Phenylketonuria: A Systematic Review and Meta-Analysis
Nutrients·2019· 32 citedOpen Access
A series of three case reports in patients with phenylketonuria performing regular exercise: first steps in dietary adjustment
Journal of Pediatric Endocrinology and Metabolism·2019· 16 citedOpen Access
Anthropomorphic measurements and nutritional biomarkers after 5 years of BH 4 treatment in phenylketonuria patients
Molecular Genetics and Metabolism·2018· 9 cited
page 1 of 2Next →

Frequent Co-authors

Anita MacDonald(18), Júlio César Rocha(17), Amaya Bélanger-Quintana(14), Francjan J. van Spronsen(14), Kirsten Ahring(12), Manuela Almeida(9), Katharina Dokoupil(9), M. Rebecca Heiner‐Fokkema(9), Anne Daly(9), Hülya Gökmen-Özel(8), Alex Pinto(8), Sharon Evans(7), François Feillet(7), Annemiek M. J. van Wegberg(7), Anna Maria Lammardo(6), Martine Robert(5), Marianne Robert(5), Margreet van Rijn(5), Pim de Blaauw(5), Foekje de Boer(5)