Francjan van Spronsen

24PUBLICATIONS
77CO-AUTHORS
Infant and child healthPreventative health careFood properties (incl. characteristics and health benefits)Applications in healthDecision making
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Publications (24)

|Jun 21, 2026
Mapping the Severity of Phenylalanine Hydroxylase Deficiency.

|Apr 09, 2026
The Role of Digital Tools and Their Implementation Within Patient Care Pathways for Rare Brain Disorders: The Case of Phenylketonuria.

Sara Cannizzo, Vinciane Quoidbach, Bernadette Sheehan-Gilroy

|Nov 11, 2025
The influence of professionals' personal views and values in the development of guidelines for rare diseases: an example from phenylketonuria.

Annemiek M J van Wegberg, Cristina Romani, Francjan J van Spronsen

|Sep 22, 2025
Correction: Kuypers et al. Evaluation of Neonatal Screening Programs for Tyrosinemia Type 1 Worldwide. Int. J. Neonatal Screen. 2024, 10, 82.

Allysa M Kuypers, Marelle J Bouva, J Gerard Loeber

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