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A Wevers

Showing results (301-310 of 543) with videos related to

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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.
Plos Pathogens|February 2, 2011
Selective C-Rel activation via Malt1 controls anti-fungal T(H)-17 immunity by dectin-1 and dectin-2Sonja I Gringhuis, Brigitte A Wevers, Tanja M Kaptein, 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|September 13, 2017
Autism spectrum disorder: an early and frequent feature in cerebrotendinous xanthomatosisBianca M L Stelten, Olivier Bonnot, Hidde H Huidekoper, et al.
NMR in Biomedicine|May 23, 2007
NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolismUdo F H Engelke, Jörn Oliver Sass, Rudy N Van Coster, 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.
Human Genetics|September 10, 1999
The frequency of lysosomal storage diseases in The NetherlandsB J Poorthuis, R A Wevers, W J Kleijer, et al.
Human Genetics|September 1, 1995
Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variantJ A Luyten, P W Wenink, G C Steenbergen-Spanjers, et al.
Pageof 55

Showing results (301-310 of 543) with videos related to

Sort By:
Pageof 55
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.
Plos Pathogens|February 2, 2011
Selective C-Rel activation via Malt1 controls anti-fungal T(H)-17 immunity by dectin-1 and dectin-2Sonja I Gringhuis, Brigitte A Wevers, Tanja M Kaptein, 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|September 13, 2017
Autism spectrum disorder: an early and frequent feature in cerebrotendinous xanthomatosisBianca M L Stelten, Olivier Bonnot, Hidde H Huidekoper, et al.
NMR in Biomedicine|May 23, 2007
NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolismUdo F H Engelke, Jörn Oliver Sass, Rudy N Van Coster, 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.
Human Genetics|September 10, 1999
The frequency of lysosomal storage diseases in The NetherlandsB J Poorthuis, R A Wevers, W J Kleijer, et al.
Human Genetics|September 1, 1995
Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variantJ A Luyten, P W Wenink, G C Steenbergen-Spanjers, et al.
Pageof 55