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A Wevers

Showing results (151-160 of 543) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1996
Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndromeM S van der Knaap, R A Wevers, L Monnens, et al.
Neuropediatrics|November 1, 1988
Acute transverse myelopathy as the initial manifestation of probable systemic lupus erythematosus in a childW H Linssen, T J Fiselier, F J Gabreëls, 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 Science (London, England : 1979)|April 1, 1987
AMP deaminase deficiency: study of the human skeletal muscle purine metabolism during ischaemic isometric exerciseS P Sinkeler, R A Binkhorst, E M Joosten, 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 Neurology, Neurosurgery, and Psychiatry|October 1, 1988
The short-term effect of an immunosuppressive treatment on CSF myelin basic protein in chronic progressive multiple sclerosisK J Lamers, B M Uitdehaag, O R Hommes, et al.
Journal of Medical Genetics|August 1, 1996
Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A geneI Redonnet-Vernhet, J K Ploos van Amstel, R P Jansen, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1987
Phenotypic expression in mucopolysaccharidosis VIIP L Bernsen, R A Wevers, F J Gabreëls, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1993
Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiencyP J Poels, R A Wevers, J P Braakhekke, et al.
Pageof 55

Showing results (151-160 of 543) with videos related to

Sort By:
Pageof 55
Journal of Inherited Metabolic Disease|January 1, 1996
Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndromeM S van der Knaap, R A Wevers, L Monnens, et al.
Neuropediatrics|November 1, 1988
Acute transverse myelopathy as the initial manifestation of probable systemic lupus erythematosus in a childW H Linssen, T J Fiselier, F J Gabreëls, 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 Science (London, England : 1979)|April 1, 1987
AMP deaminase deficiency: study of the human skeletal muscle purine metabolism during ischaemic isometric exerciseS P Sinkeler, R A Binkhorst, E M Joosten, 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 Neurology, Neurosurgery, and Psychiatry|October 1, 1988
The short-term effect of an immunosuppressive treatment on CSF myelin basic protein in chronic progressive multiple sclerosisK J Lamers, B M Uitdehaag, O R Hommes, et al.
Journal of Medical Genetics|August 1, 1996
Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A geneI Redonnet-Vernhet, J K Ploos van Amstel, R P Jansen, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1987
Phenotypic expression in mucopolysaccharidosis VIIP L Bernsen, R A Wevers, F J Gabreëls, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1993
Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiencyP J Poels, R A Wevers, J P Braakhekke, et al.
Pageof 55