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J Derks

Showing results (61-70 of 167) with videos related to

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Hepatology (Baltimore, Md.)|February 28, 2008
Inhibition of mitochondrial fatty acid oxidation in vivo only slightly suppresses gluconeogenesis but enhances clearance of glucose in miceTerry G J Derks, Theo H van Dijk, Aldo Grefhorst, et al.
The Journal of Clinical Endocrinology and Metabolism|July 5, 2022
A Prospective Study on Continuous Glucose Monitoring in Glycogen Storage Disease Type Ia: Toward Glycemic TargetsAlessandro Rossi, Annieke Venema, Petra Haarsma, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2023
Endogenous Glucose Production in Patients With Glycogen Storage Disease Type Ia Estimated by Oral D-[6,6-2H2]-glucoseAlessandro Rossi, Maaike H Oosterveer, Theo H van Dijk, et al.
European Journal of Pediatrics|June 22, 2006
Safe and unsafe duration of fasting for children with MCAD deficiencyTerry G J Derks, Francjan J van Spronsen, Jan Peter Rake, et al.
Orphanet Journal of Rare Diseases|August 26, 2020
Improved inflammatory bowel disease, wound healing and normal oxidative burst under treatment with empagliflozin in glycogen storage disease type IbSarah C Grünert, Roland Elling, Bärbel Maag, et al.
JIMD Reports|November 4, 2015
Normoglycemic Ketonemia as Biochemical Presentation in Ketotic Glycogen Storage DiseaseIrene J Hoogeveen, Rixt M van der Ende, Francjan J van Spronsen, et al.
Frontiers in Endocrinology|July 5, 2022
Dynamic Methods for Childhood Hypoglycemia Phenotyping: A Narrative ReviewAlessandro Rossi, Martijn G S Rutten, Theo H van Dijk, et al.
Reviews in Endocrine & Metabolic Disorders|March 31, 2024
Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for careAlessandro Rossi, Chiara Simeoli, Rosario Pivonello, et al.
Orphanet Journal of Rare Diseases|January 16, 2014
Single amino acid supplementation in aminoacidopathies: a systematic reviewDanique van Vliet, Terry G J Derks, Margreet van Rijn, et al.
Journal of Inherited Metabolic Disease|March 11, 2026
Untargeted Proteomics Profiling of Liver and Plasma in Fed and Fasted Liver-Specific Glycogen Storage Disease Type Ia (GSD Ia) Mice: Toward Potential Protein BiomarkersRuiqi Xiao, Hilda I de Vries, Candelas Gross-Valle, et al.
Pageof 17

Showing results (61-70 of 167) with videos related to

Sort By:
Pageof 17
Hepatology (Baltimore, Md.)|February 28, 2008
Inhibition of mitochondrial fatty acid oxidation in vivo only slightly suppresses gluconeogenesis but enhances clearance of glucose in miceTerry G J Derks, Theo H van Dijk, Aldo Grefhorst, et al.
The Journal of Clinical Endocrinology and Metabolism|July 5, 2022
A Prospective Study on Continuous Glucose Monitoring in Glycogen Storage Disease Type Ia: Toward Glycemic TargetsAlessandro Rossi, Annieke Venema, Petra Haarsma, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2023
Endogenous Glucose Production in Patients With Glycogen Storage Disease Type Ia Estimated by Oral D-[6,6-2H2]-glucoseAlessandro Rossi, Maaike H Oosterveer, Theo H van Dijk, et al.
European Journal of Pediatrics|June 22, 2006
Safe and unsafe duration of fasting for children with MCAD deficiencyTerry G J Derks, Francjan J van Spronsen, Jan Peter Rake, et al.
Orphanet Journal of Rare Diseases|August 26, 2020
Improved inflammatory bowel disease, wound healing and normal oxidative burst under treatment with empagliflozin in glycogen storage disease type IbSarah C Grünert, Roland Elling, Bärbel Maag, et al.
JIMD Reports|November 4, 2015
Normoglycemic Ketonemia as Biochemical Presentation in Ketotic Glycogen Storage DiseaseIrene J Hoogeveen, Rixt M van der Ende, Francjan J van Spronsen, et al.
Frontiers in Endocrinology|July 5, 2022
Dynamic Methods for Childhood Hypoglycemia Phenotyping: A Narrative ReviewAlessandro Rossi, Martijn G S Rutten, Theo H van Dijk, et al.
Reviews in Endocrine & Metabolic Disorders|March 31, 2024
Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for careAlessandro Rossi, Chiara Simeoli, Rosario Pivonello, et al.
Orphanet Journal of Rare Diseases|January 16, 2014
Single amino acid supplementation in aminoacidopathies: a systematic reviewDanique van Vliet, Terry G J Derks, Margreet van Rijn, et al.
Journal of Inherited Metabolic Disease|March 11, 2026
Untargeted Proteomics Profiling of Liver and Plasma in Fed and Fasted Liver-Specific Glycogen Storage Disease Type Ia (GSD Ia) Mice: Toward Potential Protein BiomarkersRuiqi Xiao, Hilda I de Vries, Candelas Gross-Valle, et al.
Pageof 17