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Orphanet Journal of Rare Diseases|February 28, 2013
Clinical pathways for inborn errors of metabolism: warranted and feasibleSerwet Demirdas, Imke N van Kessel, Marjolein J Korndewal, 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.
JIMD Reports|September 27, 2014
Infants with Tyrosinemia Type 1: Should phenylalanine be supplemented?Danique van Vliet, Esther van Dam, Margreet van Rijn, et al.
Orphanet Journal of Rare Diseases|July 12, 2013
Tetrahydrobiopterin responsiveness in phenylketonuria: prediction with the 48-hour loading test and genotypeKaren Anjema, Margreet van Rijn, Floris C Hofstede, et al.
The Lancet. Diabetes & Endocrinology|January 14, 2017
Key European guidelines for the diagnosis and management of patients with phenylketonuriaFrancjan J van Spronsen, Annemiek Mj van Wegberg, Kirsten Ahring, et al.
Journal of the American Dietetic Association|October 18, 2008
A survey of natural protein intake in Dutch phenylketonuria patients: insight into estimation or measurement of dietary intakeMargreet van Rijn, Jolanda Jansma, Aeltsje Brinksma, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 18, 2019
Dietary practices in methylmalonic acidaemia: a European surveyAlex Pinto, Sharon Evans, Anne Daly, et al.
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