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R A Wevers

Showing results (161-170 of 222) with videos related to

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Human Genetics|August 1, 1997
Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosisA Verrips, G C Steenbergen-Spanjers, J A Luyten, et al.
Brain : a Journal of Neurology|April 25, 2000
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosisA Verrips, L H Hoefsloot, G C Steenbergen, et al.
Clinical Chemistry|April 2, 1999
Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy studyS H Moolenaar, J Poggi-Bach, U F Engelke, et al.
Journal of Lipid Research|August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndromeP E Jira, R A Wevers, J de Jong, et al.
NMR in Biomedicine|May 18, 2001
In vivo and in vitro NMR spectroscopy reveal a putative novel inborn error involving polyol metabolismS H Moolenaar, M S van der Knaap, U F Engelke, et al.
Annals of Neurology|December 10, 1999
Leukoencephalopathy associated with a disturbance in the metabolism of polyolsM S van der Knaap, R A Wevers, E A Struys, et al.
Neurology|January 3, 2001
L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiencyJ F de Rijk-Van Andel, F J Gabreëls, B Geurtz, et al.
Archives of Neurology|April 18, 2000
Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosisA Verrips, B G van Engelen, R A Wevers, et al.
Archives of Neurology|April 1, 1995
Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiencyA T Hageman, F J Gabreëls, J G de Jong, et al.
Journal of Inherited Metabolic Disease|March 9, 2019
Functional disruption of pyrimidine nucleoside transporter CNT1 results in a novel inborn error of metabolism with high excretion of uridine and cytidineR A Wevers, M Christensen, U F H Engelke, et al.
Pageof 23

Showing results (161-170 of 222) with videos related to

Sort By:
Pageof 23
Human Genetics|August 1, 1997
Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosisA Verrips, G C Steenbergen-Spanjers, J A Luyten, et al.
Brain : a Journal of Neurology|April 25, 2000
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosisA Verrips, L H Hoefsloot, G C Steenbergen, et al.
Clinical Chemistry|April 2, 1999
Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy studyS H Moolenaar, J Poggi-Bach, U F Engelke, et al.
Journal of Lipid Research|August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndromeP E Jira, R A Wevers, J de Jong, et al.
NMR in Biomedicine|May 18, 2001
In vivo and in vitro NMR spectroscopy reveal a putative novel inborn error involving polyol metabolismS H Moolenaar, M S van der Knaap, U F Engelke, et al.
Annals of Neurology|December 10, 1999
Leukoencephalopathy associated with a disturbance in the metabolism of polyolsM S van der Knaap, R A Wevers, E A Struys, et al.
Neurology|January 3, 2001
L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiencyJ F de Rijk-Van Andel, F J Gabreëls, B Geurtz, et al.
Archives of Neurology|April 18, 2000
Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosisA Verrips, B G van Engelen, R A Wevers, et al.
Archives of Neurology|April 1, 1995
Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiencyA T Hageman, F J Gabreëls, J G de Jong, et al.
Journal of Inherited Metabolic Disease|March 9, 2019
Functional disruption of pyrimidine nucleoside transporter CNT1 results in a novel inborn error of metabolism with high excretion of uridine and cytidineR A Wevers, M Christensen, U F H Engelke, et al.
Pageof 23