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Journal of Inherited Metabolic Disease|January 31, 2015
Lipids in hepatic glycogen storage diseases: pathophysiology, monitoring of dietary management and future directionsTerry G J Derks, Margreet van RijnJournal of Inherited Metabolic Disease|April 8, 2010
The reality of dietary compliance in the management of phenylketonuriaAnita MacDonald, Hulya Gokmen-Ozel, Margreet van Rijn, et al.Advances in Experimental Medicine and Biology|July 30, 2017
Dietary Considerations in Tyrosinemia Type IFrancjan J van Spronsen, Margreet van Rijn, Uta Meyer, et al.Journal of Inherited Metabolic Disease|October 27, 2010
Large neutral amino acids in the treatment of PKU: from theory to practiceFrancjan J van Spronsen, Martijn J de Groot, Marieke Hoeksma, et al.Child Neurology Open|June 7, 2018
Ketogenic Diet in Refractory Childhood Epilepsy: Starting With a Liquid Formulation in an Outpatient SettingAmerins Weijenberg, Margreet van Rijn, Petra M C Callenbach, et al.Nutrition (Burbank, Los Angeles County, Calif.)|May 18, 2007
Protein metabolism in adult patients with phenylketonuriaMargreet van Rijn, Marieke Hoeksma, Pieter Sauer, et al.JIMD Reports|February 23, 2013
The ketogenic diet is well tolerated and can be effective in patients with argininosuccinate lyase deficiency and refractory epilepsyRosanne Peuscher, Monique E Dijsselhof, Nico G Abeling, et al.Molecular Genetics and Metabolism|October 11, 2011
Diurnal variations in blood phenylalanine of PKU infants under different feeding regimesMargreet van Rijn, Marieke Hoeksma, Pieter J J Sauer, et al.Annals of Nutrition & Metabolism|April 9, 2011
Adult patients with well-controlled phenylketonuria tolerate incidental additional intake of phenylalanineMargreet van Rijn, Marieke Hoeksma, Pieter J J Sauer, et al.European Journal of Pediatrics|April 15, 2003
A different approach to breast-feeding of the infant with phenylketonuriaMargreet van Rijn, Jolita Bekhof, Tietie Dijkstra, et al.Pageof 3