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R J Wanders

Showing results (241-250 of 497) with videos related to

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Prenatal Diagnosis|July 23, 1999
Complex approach to prenatal diagnosis of cytochrome c oxidase deficienciesJ Houstek, P Klement, J Hermanská, et al.
Prenatal Diagnosis|May 1, 1995
A misdiagnosis of X-linked adrenoleukodystrophy in cultured chorionic villus cells by the measurement of very long chain fatty acidsR G Gray, A Green, T Cole, et al.
Tijdschrift Voor Kindergeneeskunde|December 1, 1984
[Diagnosis of Zellweger's cerebrohepatorenal syndrome]R B Schutgens, H S Heymans, R Purvis, et al.
Biochimie|January 1, 1993
Ether lipid synthesis and its deficiency in peroxisomal disordersH van den Bosch, G Schrakamp, D Hardeman, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Metabolic aspects of peroxisomal disordersR J Wanders, G Jansen, C W van Roermund, et al.
Pediatric Research|August 14, 1998
Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disordersE Schmidt-Sommerfeld, P J Bobrowski, D Penn, et al.
Journal of Lipid Research|December 10, 1999
Phytanoyl-CoA hydroxylase from rat liver. Protein purification and cDNA cloning with implications for the subcellular localization of phytanic acid alpha-oxidationG A Jansen, R Ofman, S Denis, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A new peroxisomal disorder: di- and trihydroxycholestanaemia due to a presumed trihydroxycholestanoyl-CoA oxidase deficiencyE Christensen, J Van Eldere, N J Brandt, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Antenatal diagnosis of rhizomelic chondrodysplasia punctata in the second trimesterR G Gray, A Green, R B Schutgens, et al.
Biochemical Society Transactions|October 10, 1998
The non-specific lipid transfer protein (sterol carrier protein 2) acts as a peroxisomal fatty acyl-CoA binding proteinK W Wirtz, F S Wouters, P H Bastiaens, et al.
Pageof 50

Showing results (241-250 of 497) with videos related to

Sort By:
Pageof 50
Prenatal Diagnosis|July 23, 1999
Complex approach to prenatal diagnosis of cytochrome c oxidase deficienciesJ Houstek, P Klement, J Hermanská, et al.
Prenatal Diagnosis|May 1, 1995
A misdiagnosis of X-linked adrenoleukodystrophy in cultured chorionic villus cells by the measurement of very long chain fatty acidsR G Gray, A Green, T Cole, et al.
Tijdschrift Voor Kindergeneeskunde|December 1, 1984
[Diagnosis of Zellweger's cerebrohepatorenal syndrome]R B Schutgens, H S Heymans, R Purvis, et al.
Biochimie|January 1, 1993
Ether lipid synthesis and its deficiency in peroxisomal disordersH van den Bosch, G Schrakamp, D Hardeman, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Metabolic aspects of peroxisomal disordersR J Wanders, G Jansen, C W van Roermund, et al.
Pediatric Research|August 14, 1998
Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disordersE Schmidt-Sommerfeld, P J Bobrowski, D Penn, et al.
Journal of Lipid Research|December 10, 1999
Phytanoyl-CoA hydroxylase from rat liver. Protein purification and cDNA cloning with implications for the subcellular localization of phytanic acid alpha-oxidationG A Jansen, R Ofman, S Denis, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A new peroxisomal disorder: di- and trihydroxycholestanaemia due to a presumed trihydroxycholestanoyl-CoA oxidase deficiencyE Christensen, J Van Eldere, N J Brandt, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Antenatal diagnosis of rhizomelic chondrodysplasia punctata in the second trimesterR G Gray, A Green, R B Schutgens, et al.
Biochemical Society Transactions|October 10, 1998
The non-specific lipid transfer protein (sterol carrier protein 2) acts as a peroxisomal fatty acyl-CoA binding proteinK W Wirtz, F S Wouters, P H Bastiaens, et al.
Pageof 50