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Ron A Wevers

Showing results (41-50 of 266) with videos related to

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Annals of Neurology|September 24, 2005
Pipecolic acid: a diagnostic marker in pyridoxine-dependent epilepsyMichèl A A P Willemsen, Annelies M C Mavinkurve-Groothuis, Ron A Wevers, et al.
Analytical Chemistry|July 14, 2015
Quantitative measurement of immunoglobulins and free light chains using mass spectrometryMartijn M VanDuijn, Joannes F M Jacobs, Ron A Wevers, et al.
Clinical Physiology and Functional Imaging|June 22, 2002
In vivo quantitative near-infrared spectroscopy in skeletal muscle during incremental isometric handgrip exerciseMireille C P van Beekvelt, Baziel G M van Engelen, Ron A Wevers, et al.
Journal of Proteome Research|February 3, 2007
Proteomics approaches to study genetic and metabolic disordersJolein Gloerich, Ron A Wevers, Jan A M Smeitink, et al.
Amino Acids|July 13, 2016
Monitoring creatine and phosphocreatine by (13)C MR spectroscopic imaging during and after (13)C4 creatine loading: a feasibility studyBarbara H Janssen, Saskia Lassche, Maria T Hopman, et al.
Neuropediatrics|May 25, 2012
Glucose transporter-1 (GLUT1) deficiency syndrome: diagnosis and treatment in late childhoodGwendolyn Gramer, Nicole I Wolf, Daniel Vater, et al.
Plos One|May 11, 2018
The 1H-NMR-based metabolite profile of acute alcohol consumption: A metabolomics intervention studyCindy Irwin, Mari van Reenen, Shayne Mason, et al.
European Journal of Pediatrics|January 18, 2006
CDG: a new case of a combined defect in the biosynthesis of N- and O-glycansZiad Albahri, Eliska Marklová, Petr Dedek, et al.
Journal of Inherited Metabolic Disease|January 9, 2013
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclatureSaskia B Wortmann, Marinus Duran, Yair Anikster, et al.
Glycobiology|July 23, 2005
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groupsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
Pageof 27

Showing results (41-50 of 266) with videos related to

Sort By:
Pageof 27
Annals of Neurology|September 24, 2005
Pipecolic acid: a diagnostic marker in pyridoxine-dependent epilepsyMichèl A A P Willemsen, Annelies M C Mavinkurve-Groothuis, Ron A Wevers, et al.
Analytical Chemistry|July 14, 2015
Quantitative measurement of immunoglobulins and free light chains using mass spectrometryMartijn M VanDuijn, Joannes F M Jacobs, Ron A Wevers, et al.
Clinical Physiology and Functional Imaging|June 22, 2002
In vivo quantitative near-infrared spectroscopy in skeletal muscle during incremental isometric handgrip exerciseMireille C P van Beekvelt, Baziel G M van Engelen, Ron A Wevers, et al.
Journal of Proteome Research|February 3, 2007
Proteomics approaches to study genetic and metabolic disordersJolein Gloerich, Ron A Wevers, Jan A M Smeitink, et al.
Amino Acids|July 13, 2016
Monitoring creatine and phosphocreatine by (13)C MR spectroscopic imaging during and after (13)C4 creatine loading: a feasibility studyBarbara H Janssen, Saskia Lassche, Maria T Hopman, et al.
Neuropediatrics|May 25, 2012
Glucose transporter-1 (GLUT1) deficiency syndrome: diagnosis and treatment in late childhoodGwendolyn Gramer, Nicole I Wolf, Daniel Vater, et al.
Plos One|May 11, 2018
The 1H-NMR-based metabolite profile of acute alcohol consumption: A metabolomics intervention studyCindy Irwin, Mari van Reenen, Shayne Mason, et al.
European Journal of Pediatrics|January 18, 2006
CDG: a new case of a combined defect in the biosynthesis of N- and O-glycansZiad Albahri, Eliska Marklová, Petr Dedek, et al.
Journal of Inherited Metabolic Disease|January 9, 2013
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclatureSaskia B Wortmann, Marinus Duran, Yair Anikster, et al.
Glycobiology|July 23, 2005
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groupsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
Pageof 27