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Neonatology
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April 24, 2010
Sweet and sour aspects of medium-chain acyl CoA dehydrogenase deficiency. Commentary on K. Yusuf et al.: Neonatal ventricular tachyarrhythmias in medium chain acyl-CoA dehydrogenase deficiency (Neonatology 2010;98:260-264)
Terry G J Derks
Journal of Inherited Metabolic Disease
|
January 31, 2015
Lipids in hepatic glycogen storage diseases: pathophysiology, monitoring of dietary management and future directions
Terry 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
Lancet (London, England)
|
April 19, 2014
Recombinant phenylalanine ammonia lyase in phenylketonuria
Francjan J van Spronsen, Terry G J Derks
Journal of Inherited Metabolic Disease
|
November 25, 2018
Next-generation glycogen storage diseases
Terry G J Derks, Maaike H Oosterveer, Carolina F De Souza
Acta Paediatrica (Oslo, Norway : 1992)
|
March 4, 2025
Is the Proof of the Pudding in the Fasting When It Comes to Rare Inherited Mitochondrial Fatty Acid Oxidation Disorders?
Andrea B Haijer-Schreuder, Emmalie A Jager, Terry G J Derks
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 Diseases
Terry G J Derks, Ruben J Overduin, Sarah C Grünert, et al.
Journal of Inherited Metabolic Disease
|
September 11, 2022
Towards values-based healthcare for inherited metabolic disorders: An overview of current practices for persons with liver glycogen storage disease and fatty acid oxidation disorders
Annieke Venema, Fabian Peeks, Alessandro Rossi, et al.
Pediatric Clinics of North America
|
March 6, 2018
Inborn Errors of Metabolism with Hypoglycemia: Glycogen Storage Diseases and Inherited Disorders of Gluconeogenesis
David A Weinstein, Ulrike Steuerwald, Carolina F M De Souza, et al.
Journal of Inherited Metabolic Disease
|
April 30, 2015
Determination of amylose/amylopectin ratio of starches
Tatiéle Nalin, Fernanda Sperb-Ludwig, Koen Venema, et al.
Page
of 12
Search research articles
Search
Showing results (1-10 of 111) with videos related to
Sort By:
Page
of 12
Neonatology
|
April 24, 2010
Sweet and sour aspects of medium-chain acyl CoA dehydrogenase deficiency. Commentary on K. Yusuf et al.: Neonatal ventricular tachyarrhythmias in medium chain acyl-CoA dehydrogenase deficiency (Neonatology 2010;98:260-264)
Terry G J Derks
Journal of Inherited Metabolic Disease
|
January 31, 2015
Lipids in hepatic glycogen storage diseases: pathophysiology, monitoring of dietary management and future directions
Terry 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
Lancet (London, England)
|
April 19, 2014
Recombinant phenylalanine ammonia lyase in phenylketonuria
Francjan J van Spronsen, Terry G J Derks
Journal of Inherited Metabolic Disease
|
November 25, 2018
Next-generation glycogen storage diseases
Terry G J Derks, Maaike H Oosterveer, Carolina F De Souza
Acta Paediatrica (Oslo, Norway : 1992)
|
March 4, 2025
Is the Proof of the Pudding in the Fasting When It Comes to Rare Inherited Mitochondrial Fatty Acid Oxidation Disorders?
Andrea B Haijer-Schreuder, Emmalie A Jager, Terry G J Derks
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 Diseases
Terry G J Derks, Ruben J Overduin, Sarah C Grünert, et al.
Journal of Inherited Metabolic Disease
|
September 11, 2022
Towards values-based healthcare for inherited metabolic disorders: An overview of current practices for persons with liver glycogen storage disease and fatty acid oxidation disorders
Annieke Venema, Fabian Peeks, Alessandro Rossi, et al.
Pediatric Clinics of North America
|
March 6, 2018
Inborn Errors of Metabolism with Hypoglycemia: Glycogen Storage Diseases and Inherited Disorders of Gluconeogenesis
David A Weinstein, Ulrike Steuerwald, Carolina F M De Souza, et al.
Journal of Inherited Metabolic Disease
|
April 30, 2015
Determination of amylose/amylopectin ratio of starches
Tatiéle Nalin, Fernanda Sperb-Ludwig, Koen Venema, et al.
Page
of 12