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Journal of Inherited Metabolic Disease|August 29, 2014
Dietary management in glycogen storage disease type III: what is the evidence?Terry G J Derks, G Peter A Smit
European Journal of Pediatrics|October 10, 2002
Disturbed lipid metabolism in glycogen storage disease type 1Robert H J Bandsma, G Peter A Smit, Folkert Kuipers
JIMD Reports|February 23, 2013
Heart Failure Due to Severe Hypertrophic Cardiomyopathy Reversed by Low Calorie, High Protein Dietary Adjustments in a Glycogen Storage Disease Type IIIa PatientChristiaan P Sentner, Kadir Caliskan, Wim B Vletter, et al.
European Journal of Pediatrics|October 10, 2002
Guidelines for management of glycogen storage disease type I - European Study on Glycogen Storage Disease Type I (ESGSD I)Jan Peter Rake, Gepke Visser, Philippe Labrune, et al.
European Journal of Pediatrics|October 10, 2002
Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I)Jan Peter Rake, Gepke Visser, Philippe Labrune, et al.
JIMD Reports|February 23, 2013
Mutation Analysis in Glycogen Storage Disease Type III Patients in the Netherlands: Novel Genotype-Phenotype Relationships and Five Novel Mutations in the AGL GeneChristiaan P Sentner, Yvonne J Vos, Klary N Niezen-Koning, et al.
European Journal of Pediatrics|October 10, 2002
Is glycogen storage disease 1a associated with atherosclerosis?Froukje L Ubels, Jan Peter Rake, Joris P J Slaets, et al.
Kidney International|April 11, 2014
Targeted deletion of kidney glucose-6 phosphatase leads to nephropathyJulie Clar, Blandine Gri, Julien Calderaro, et al.
The Journal of Pediatrics|July 24, 2007
Cost-effectiveness of neonatal screening for medium chain acyl-CoA dehydrogenase deficiency: the homogeneous population of The NetherlandsChristian S van der Hilst, Terry G J Derks, Dirk-Jan Reijngoud, et al.
European Journal of Pediatrics|October 10, 2002
Consensus guidelines for management of glycogen storage disease type 1b - European Study on Glycogen Storage Disease Type 1Gepke Visser, Jan Peter Rake, Philippe Labrune, et al.
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