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A Wevers

Showing results (71-80 of 543) with videos related to

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Journal of Inherited Metabolic Disease|March 25, 2011
Metabolic cutis laxa syndromesMiski Mohamed, Dorus Kouwenberg, Thatjana Gardeitchik, et al.
Journal of Neurology|May 1, 1993
Decreased vitamin B12 and folate levels in cerebrospinal fluid and serum of multiple sclerosis patients after high-dose intravenous methylprednisoloneS T Frequin, R A Wevers, M Braam, et al.
European Journal of Pediatrics|July 21, 1999
Long-term follow up of a new case of hawkinsinuriaW Lehnert, W Stögmann, U Engelke, et al.
Journal of Vascular Surgery|April 1, 1993
Intestinal permeability is increased after major vascular surgeryR M Roumen, J A van der Vliet, R A Wevers, et al.
Journal of Inherited Metabolic Disease|November 16, 2024
A Dutch translational knowledge agenda for inherited metabolic diseasesHans R Waterham, Ronald J A Wanders, Ron A Wevers, et al.
Annals of the New York Academy of Sciences|July 9, 2004
Congenital dopamine-beta-hydroxylase deficiency in humansH J L M Timmers, J Deinum, R A Wevers, et al.
Neurology|October 27, 2004
Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiencyA Schiller, R A Wevers, G C H Steenbergen, et al.
Pediatric Neurology|May 31, 2017
Cerebellar Disease Mimicking Cerebrotendinous Xanthomatosis: Langerhans Cell HistiocytosisBianca M L Stelten, Marjo S van der Knaap, Ron A Wevers, et al.
Journal of Pharmaceutical and Biomedical Analysis|June 2, 2017
<sup>1</sup>H NMR spectral identification of medication in cerebrospinal fluid of pediatric meningitisShayne Mason, Carolus J Reinecke, Regan Solomons, et al.
JIMD Reports|April 24, 2014
Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH DefectSaskia B Wortmann, Leo A J Kluijtmans, Silvia Sequeira, et al.
Pageof 55

Showing results (71-80 of 543) with videos related to

Sort By:
Pageof 55
Journal of Inherited Metabolic Disease|March 25, 2011
Metabolic cutis laxa syndromesMiski Mohamed, Dorus Kouwenberg, Thatjana Gardeitchik, et al.
Journal of Neurology|May 1, 1993
Decreased vitamin B12 and folate levels in cerebrospinal fluid and serum of multiple sclerosis patients after high-dose intravenous methylprednisoloneS T Frequin, R A Wevers, M Braam, et al.
European Journal of Pediatrics|July 21, 1999
Long-term follow up of a new case of hawkinsinuriaW Lehnert, W Stögmann, U Engelke, et al.
Journal of Vascular Surgery|April 1, 1993
Intestinal permeability is increased after major vascular surgeryR M Roumen, J A van der Vliet, R A Wevers, et al.
Journal of Inherited Metabolic Disease|November 16, 2024
A Dutch translational knowledge agenda for inherited metabolic diseasesHans R Waterham, Ronald J A Wanders, Ron A Wevers, et al.
Annals of the New York Academy of Sciences|July 9, 2004
Congenital dopamine-beta-hydroxylase deficiency in humansH J L M Timmers, J Deinum, R A Wevers, et al.
Neurology|October 27, 2004
Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiencyA Schiller, R A Wevers, G C H Steenbergen, et al.
Pediatric Neurology|May 31, 2017
Cerebellar Disease Mimicking Cerebrotendinous Xanthomatosis: Langerhans Cell HistiocytosisBianca M L Stelten, Marjo S van der Knaap, Ron A Wevers, et al.
Journal of Pharmaceutical and Biomedical Analysis|June 2, 2017
<sup>1</sup>H NMR spectral identification of medication in cerebrospinal fluid of pediatric meningitisShayne Mason, Carolus J Reinecke, Regan Solomons, et al.
JIMD Reports|April 24, 2014
Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH DefectSaskia B Wortmann, Leo A J Kluijtmans, Silvia Sequeira, et al.
Pageof 55