Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N M Verhoeven

Showing results (11-20 of 63) with videos related to

Pageof 7
Sort By:
Journal of Inherited Metabolic Disease|November 20, 1998
The metabolism of phytanic acid and pristanic acid in man: a reviewN M Verhoeven, R J Wanders, B T Poll-The, et al.
Biochemical and Biophysical Research Communications|August 8, 1997
Resolution of the phytanic acid alpha-oxidation pathway: identification of pristanal as product of the decarboxylation of 2-hydroxyphytanoyl-CoAN M Verhoeven, D S Schor, H J ten Brink, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|October 18, 2002
Quantification of 3-hydroxyglutaric acid in urine, plasma, cerebrospinal fluid and amniotic fluid by stable-isotope dilution negative chemical ionization gas chromatography-mass spectrometryD S M Schor, N M Verhoeven, E A Struys, et al.
FEBS Letters|July 14, 1998
Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acidN M Verhoeven, C Jakobs, G Carney, et al.
Molecular Genetics and Metabolism|October 3, 2002
L-Arabinosuria: a new defect in human pentose metabolismW Onkenhout, J E M Groener, N M Verhoeven, et al.
Advances in Experimental Medicine and Biology|March 10, 2000
Phytanoyl-CoA hydroxylase deficiency. Enzymological and molecular basis of classical Refsum diseaseG A Jansen, S Ferdinandusse, E M Hogenhout, et al.
Journal of Inherited Metabolic Disease|July 3, 2007
Detection of transaldolase deficiency by quantification of novel seven-carbon chain carbohydrate biomarkers in urineM M Wamelink, D E Smith, E E Jansen, et al.
Journal of Lipid Research|February 20, 1998
Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblastsN M Verhoeven, D S Roe, R M Kok, et al.
Neurology|August 23, 2006
Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiencyA Schulze, G F Hoffmann, P Bachert, et al.
Biochimica Et Biophysica Acta|July 21, 1993
Cloning of the cDNA coding for 14 kDa group II phospholipase A2 from rat liverR H Van Schaik, N M Verhoeven, F W Neijs, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Journal of Inherited Metabolic Disease|November 20, 1998
The metabolism of phytanic acid and pristanic acid in man: a reviewN M Verhoeven, R J Wanders, B T Poll-The, et al.
Biochemical and Biophysical Research Communications|August 8, 1997
Resolution of the phytanic acid alpha-oxidation pathway: identification of pristanal as product of the decarboxylation of 2-hydroxyphytanoyl-CoAN M Verhoeven, D S Schor, H J ten Brink, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|October 18, 2002
Quantification of 3-hydroxyglutaric acid in urine, plasma, cerebrospinal fluid and amniotic fluid by stable-isotope dilution negative chemical ionization gas chromatography-mass spectrometryD S M Schor, N M Verhoeven, E A Struys, et al.
FEBS Letters|July 14, 1998
Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acidN M Verhoeven, C Jakobs, G Carney, et al.
Molecular Genetics and Metabolism|October 3, 2002
L-Arabinosuria: a new defect in human pentose metabolismW Onkenhout, J E M Groener, N M Verhoeven, et al.
Advances in Experimental Medicine and Biology|March 10, 2000
Phytanoyl-CoA hydroxylase deficiency. Enzymological and molecular basis of classical Refsum diseaseG A Jansen, S Ferdinandusse, E M Hogenhout, et al.
Journal of Inherited Metabolic Disease|July 3, 2007
Detection of transaldolase deficiency by quantification of novel seven-carbon chain carbohydrate biomarkers in urineM M Wamelink, D E Smith, E E Jansen, et al.
Journal of Lipid Research|February 20, 1998
Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblastsN M Verhoeven, D S Roe, R M Kok, et al.
Neurology|August 23, 2006
Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiencyA Schulze, G F Hoffmann, P Bachert, et al.
Biochimica Et Biophysica Acta|July 21, 1993
Cloning of the cDNA coding for 14 kDa group II phospholipase A2 from rat liverR H Van Schaik, N M Verhoeven, F W Neijs, et al.
Pageof 7