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A Wevers

Showing results (251-260 of 543) with videos related to

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Annals of Clinical Biochemistry|January 25, 2003
Cobalamin-binding proteins in normal and cobalamin-deficient older subjectsDieneke Z B van Asselt, Chris M G Thomas, Martin F G Segers, et al.
Journal of Inherited Metabolic Disease|September 21, 2010
Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotypeMarlies J Valstar, Hennie T Bruggenwirth, Renske Olmer, et al.
Biochimica Et Biophysica Acta|October 19, 1999
beta-Trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brainS Grünewald, K Huyben, J G de Jong, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Pathobiochemical implications of hyperdopaminuria in patients with aromatic L-amino acid decarboxylase deficiencyN G Abeling, C Bräutigam, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|January 24, 2002
Detection of beta-ureidopropionase deficiency with HPLC-electrospray tandem mass spectrometry and confirmation of the defect at the enzyme levelA B Van Kuilenburg, H Van Lenthe, B Assmann, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 15, 2013
Alpha-fetoprotein, a fascinating protein and biomarker in neurologyJ H Schieving, M de Vries, J M G van Vugt, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Paediatric cerebrotendinous xanthomatosisR A Wevers, J R Cruysberg, A F Van Heijst, et al.
The Journal of Pediatrics|February 7, 2001
Tyrosine hydroxylase deficiency with severe clinical course: clinical and biochemical investigations and optimization of therapyC Dionisi-Vici, G F Hoffmann, V Leuzzi, et al.
Clinical Chemistry|December 16, 2006
Transferrin and apolipoprotein C-III isofocusing are complementary in the diagnosis of N- and O-glycan biosynthesis defectsSuzan Wopereis, Stephanie Grünewald, Karin M L C Huijben, et al.
Metabolites|November 20, 2020
Variable Selection in Untargeted Metabolomics and the Danger of SparsityGerjen H Tinnevelt, Udo F H Engelke, Ron A Wevers, et al.
Pageof 55

Showing results (251-260 of 543) with videos related to

Sort By:
Pageof 55
Annals of Clinical Biochemistry|January 25, 2003
Cobalamin-binding proteins in normal and cobalamin-deficient older subjectsDieneke Z B van Asselt, Chris M G Thomas, Martin F G Segers, et al.
Journal of Inherited Metabolic Disease|September 21, 2010
Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotypeMarlies J Valstar, Hennie T Bruggenwirth, Renske Olmer, et al.
Biochimica Et Biophysica Acta|October 19, 1999
beta-Trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brainS Grünewald, K Huyben, J G de Jong, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Pathobiochemical implications of hyperdopaminuria in patients with aromatic L-amino acid decarboxylase deficiencyN G Abeling, C Bräutigam, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|January 24, 2002
Detection of beta-ureidopropionase deficiency with HPLC-electrospray tandem mass spectrometry and confirmation of the defect at the enzyme levelA B Van Kuilenburg, H Van Lenthe, B Assmann, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 15, 2013
Alpha-fetoprotein, a fascinating protein and biomarker in neurologyJ H Schieving, M de Vries, J M G van Vugt, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Paediatric cerebrotendinous xanthomatosisR A Wevers, J R Cruysberg, A F Van Heijst, et al.
The Journal of Pediatrics|February 7, 2001
Tyrosine hydroxylase deficiency with severe clinical course: clinical and biochemical investigations and optimization of therapyC Dionisi-Vici, G F Hoffmann, V Leuzzi, et al.
Clinical Chemistry|December 16, 2006
Transferrin and apolipoprotein C-III isofocusing are complementary in the diagnosis of N- and O-glycan biosynthesis defectsSuzan Wopereis, Stephanie Grünewald, Karin M L C Huijben, et al.
Metabolites|November 20, 2020
Variable Selection in Untargeted Metabolomics and the Danger of SparsityGerjen H Tinnevelt, Udo F H Engelke, Ron A Wevers, et al.
Pageof 55