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A Wevers

Showing results (261-270 of 543) with videos related to

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Molecular Genetics and Metabolism|May 20, 2008
PNPO deficiency: an under diagnosed inborn error of pyridoxine metabolismMorad Khayat, Stanley H Korman, Pnina Frankel, et al.
Analytical Chemistry|February 3, 2023
Targeted Small-Molecule Identification Using Heartcutting Liquid Chromatography-Infrared Ion SpectroscopyRianne E van Outersterp, Jitse Oosterhout, Christoph R Gebhardt, et al.
Biochimica Et Biophysica Acta|June 16, 2005
A combined defect in the biosynthesis of N- and O-glycans in patients with cutis laxa and neurological involvement: the biochemical characteristicsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
Clinical Neuropathology|November 16, 2010
Clinical imaging and neuropathological correlations in an unusual case of cerebrotendinous xanthomatosisD Wallon, L Guyant-Maréchal, A Laquerrière, et al.
Neuropediatrics|May 8, 2026
Unmasking Complex Chromosomal Rearrangement Impacting CHD2 by Genome Sequencing and Optical Genome Mapping in Developmental and Epileptic Encephalopathy-DEE94Robin Wijngaard, Pinelopi Dragoumi, Kornelia Neveling, et al.
Clinical Neuropathology|February 24, 2010
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathyN C Voermans, M Guillard, R Doedée, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
1H NMR spectroscopy of body fluids in patients with inborn errors of purine and pyrimidine metabolismR A Wevers, U Engelke, J J Rotteveel, et al.
The Netherlands Journal of Medicine|June 23, 2000
Normal carnitine levels in patients with chronic fatigue syndromeP M Soetekouw, R A Wevers, P Vreken, et al.
Radiology|December 9, 2000
Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findingsF Barkhof, A Verrips, P Wesseling, et al.
Neurobiology of Disease|December 15, 2000
Cellular expression of alpha7 nicotinic acetylcholine receptor protein in the temporal cortex in Alzheimer's and Parkinson's disease--a stereological approachC Banerjee, J R Nyengaard, A Wevers, et al.
Pageof 55

Showing results (261-270 of 543) with videos related to

Sort By:
Pageof 55
Molecular Genetics and Metabolism|May 20, 2008
PNPO deficiency: an under diagnosed inborn error of pyridoxine metabolismMorad Khayat, Stanley H Korman, Pnina Frankel, et al.
Analytical Chemistry|February 3, 2023
Targeted Small-Molecule Identification Using Heartcutting Liquid Chromatography-Infrared Ion SpectroscopyRianne E van Outersterp, Jitse Oosterhout, Christoph R Gebhardt, et al.
Biochimica Et Biophysica Acta|June 16, 2005
A combined defect in the biosynthesis of N- and O-glycans in patients with cutis laxa and neurological involvement: the biochemical characteristicsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
Clinical Neuropathology|November 16, 2010
Clinical imaging and neuropathological correlations in an unusual case of cerebrotendinous xanthomatosisD Wallon, L Guyant-Maréchal, A Laquerrière, et al.
Neuropediatrics|May 8, 2026
Unmasking Complex Chromosomal Rearrangement Impacting CHD2 by Genome Sequencing and Optical Genome Mapping in Developmental and Epileptic Encephalopathy-DEE94Robin Wijngaard, Pinelopi Dragoumi, Kornelia Neveling, et al.
Clinical Neuropathology|February 24, 2010
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathyN C Voermans, M Guillard, R Doedée, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
1H NMR spectroscopy of body fluids in patients with inborn errors of purine and pyrimidine metabolismR A Wevers, U Engelke, J J Rotteveel, et al.
The Netherlands Journal of Medicine|June 23, 2000
Normal carnitine levels in patients with chronic fatigue syndromeP M Soetekouw, R A Wevers, P Vreken, et al.
Radiology|December 9, 2000
Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findingsF Barkhof, A Verrips, P Wesseling, et al.
Neurobiology of Disease|December 15, 2000
Cellular expression of alpha7 nicotinic acetylcholine receptor protein in the temporal cortex in Alzheimer's and Parkinson's disease--a stereological approachC Banerjee, J R Nyengaard, A Wevers, et al.
Pageof 55