Verhoeven NM et al. |
Analysis of pristanic acid beta-oxidation intermediates in plasma from healthy controls and patients affected with peroxisomal disorders by stable isotope dilution gas chromatography mass spectrometry. |
1999 |
J. Lipid Res. |
pmid:9925655
|
van Grunsven EG et al. |
Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis. |
1999 |
Am. J. Hum. Genet. |
pmid:9915948
|
Verhoeven NM et al. |
Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysis. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9819705
|
Verhoeven NM et al. |
The metabolism of phytanic acid and pristanic acid in man: a review. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9819701
|
Vreken P et al. |
Rapid stable isotope dilution analysis of very-long-chain fatty acids, pristanic acid and phytanic acid using gas chromatography-electron impact mass spectrometry. |
1998 |
J. Chromatogr. B Biomed. Sci. Appl. |
pmid:9746242
|
Wanders RJ et al. |
Identification of the newly discovered 58 kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: implications for peroxisomal beta-oxidation disorders. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9686381
|
Verhoeven NM et al. |
Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acid. |
1998 |
FEBS Lett. |
pmid:9662422
|
Sequeira JS et al. |
Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9584266
|
Verhoeven NM et al. |
Pristanic acid beta-oxidation in peroxisomal disorders: studies in cultured human fibroblasts. |
1998 |
Biochim. Biophys. Acta |
pmid:9555092
|
Verhoeven NM et al. |
Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts. |
1998 |
J. Lipid Res. |
pmid:9469587
|
Verhoeven NM et al. |
Phytanic acid alpha-oxidation: decarboxylation of 2-hydroxyphytanoyl-CoA to pristanic acid in human liver. |
1997 |
J. Lipid Res. |
pmid:9374128
|
Verhoeven NM et al. |
Resolution of the phytanic acid alpha-oxidation pathway: identification of pristanal as product of the decarboxylation of 2-hydroxyphytanoyl-CoA. |
1997 |
Biochem. Biophys. Res. Commun. |
pmid:9266824
|
Verhoeven NM et al. |
Formation of 2,3-pristenic acid and 3-hydroxypristanic acid from pristanic acid in human liver. |
1997 |
J. Inherit. Metab. Dis. |
pmid:9266376
|
van Grunsven EG and Wanders RJ |
Genetic heterogeneity in patients with a disorder of peroxisomal beta-oxidation: a complementation study based on pristanic acid beta-oxidation suggesting different enzyme defects. |
1997 |
J. Inherit. Metab. Dis. |
pmid:9266375
|
Dieuaide-Noubhani M et al. |
Evidence that multifunctional protein 2, and not multifunctional protein 1, is involved in the peroxisomal beta-oxidation of pristanic acid. |
1997 |
Biochem. J. |
pmid:9230115
|
van Grunsven EG et al. |
Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein. |
1997 |
Biochem. Biophys. Res. Commun. |
pmid:9196058
|
Dacremont G et al. |
Measurement of very long-chain fatty acids, phytanic and pristanic acid in plasma and cultured fibroblasts by gas chromatography. |
1995 |
J. Inherit. Metab. Dis. |
pmid:9053557
|
Verhoeven NM et al. |
Pre- and postnatal diagnosis of peroxisomal disorders using stable-isotope dilution gas chromatography--mass spectrometry. |
1995 |
J. Inherit. Metab. Dis. |
pmid:9053555
|
Wanders RJ et al. |
Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts. |
1995 |
J. Inherit. Metab. Dis. |
pmid:9053546
|
Mota CR et al. |
Rhizomelic chondrodysplasia punctata-like phenotype in a newborn male with normal peroxisomal function. |
1997 |
J Pediatr Orthop B |
pmid:9039662
|