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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 Rijn
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
Journal of Inherited Metabolic Disease|May 13, 2025
State of the Art and Consensus Statements by Healthcare Providers, Patients, and Caregivers on Continuous Glucose Monitoring in Liver Glycogen Storage DiseasesTerry G J Derks, Ruben J Overduin, Sarah C Grünert, et al.
Pediatric Clinics of North America|March 6, 2018
Inborn Errors of Metabolism with Hypoglycemia: Glycogen Storage Diseases and Inherited Disorders of GluconeogenesisDavid A Weinstein, Ulrike Steuerwald, Carolina F M De Souza, et al.
Molecular Genetics and Metabolism|May 9, 2026
Clinical and biochemical footprints of inherited metabolic disorders: XIX. HypoglycemiaAlessandro Rossi, Gianni Bocca, Dennis K Bos, et al.
Hormone Research in Paediatrics|March 21, 2024
Idiopathic Pathological Ketotic Hypoglycemia: Finding the Needle in a HaystackJoseph I Wolfsdorf, Terry G J Derks, Danielle Drachmann, et al.
Journal of Inherited Metabolic Disease|July 2, 2022
Plasma carnitine concentrations in Medium-chain acyl-CoA dehydrogenase deficiency: lessons from an observational cohort studyEmmalie A Jager, Merit Schaafsma, Melanie M van der Klauw, et al.
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