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Marinus Duran

Showing results (1-10 of 72) with videos related to

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Journal of Inherited Metabolic Disease|November 25, 2010
Enzymology of the branched-chain amino acid oxidation disorders: the valine pathwayRonald J A Wanders, Marinus Duran, Ference J Loupatty
The Journal of Biological Chemistry|March 21, 2006
Omega-oxidation of very long-chain fatty acids in human liver microsomes. Implications for X-linked adrenoleukodystrophyRobert-Jan Sanders, Rob Ofman, Marinus Duran, et al.
BMJ Case Reports|June 29, 2011
Neonatal carnitine palmitoyltransferase II deficiency: failure of treatment despite prolonged survivalPetra Hissink-Muller, Enrico Lopriore, Carolien Boelen, et al.
Clinical Chemistry|December 20, 2003
Quantification of free sialic acid in urine by HPLC-electrospray tandem mass spectrometry: a tool for the diagnosis of sialic acid storage diseaseFredoen Valianpour, Nicolaas G G M Abeling, Marinus Duran, et al.
Pediatric Research|March 21, 2003
Characteristic acylcarnitine profiles in inherited defects of peroxisome biogenesis: a novel tool for screening diagnosis using tandem mass spectrometryCristiano Rizzo, Sara Boenzi, Ronald J A Wanders, et al.
European Journal of Pediatrics|October 16, 2007
Fasting adaptation in idiopathic ketotic hypoglycemia: a mismatch between glucose production and demandHidde H Huidekoper, Marinus Duran, Marjolein Turkenburg, et al.
Pediatric Research|December 3, 2009
Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiencyBianca T van Maldegem, Marinus Duran, Ronald J A Wanders, et al.
The Biochemical Journal|January 22, 2003
L-serine in disease and developmentTom J de Koning, Keith Snell, Marinus Duran, et al.
AJNR. American Journal of Neuroradiology|January 20, 2004
Neonatal citrullinemia: comparison of conventional MR, diffusion-weighted, and diffusion tensor findingsCharles B L M Majoie, Jeroen M Mourmans, Erik M Akkerman, et al.
American Journal of Human Genetics|November 16, 2002
3-Methylglutaconic aciduria type I is caused by mutations in AUHLodewijk IJlst, Ference J Loupatty, Jos P N Ruiter, et al.
Pageof 8

Showing results (1-10 of 72) with videos related to

Sort By:
Pageof 8
Journal of Inherited Metabolic Disease|November 25, 2010
Enzymology of the branched-chain amino acid oxidation disorders: the valine pathwayRonald J A Wanders, Marinus Duran, Ference J Loupatty
The Journal of Biological Chemistry|March 21, 2006
Omega-oxidation of very long-chain fatty acids in human liver microsomes. Implications for X-linked adrenoleukodystrophyRobert-Jan Sanders, Rob Ofman, Marinus Duran, et al.
BMJ Case Reports|June 29, 2011
Neonatal carnitine palmitoyltransferase II deficiency: failure of treatment despite prolonged survivalPetra Hissink-Muller, Enrico Lopriore, Carolien Boelen, et al.
Clinical Chemistry|December 20, 2003
Quantification of free sialic acid in urine by HPLC-electrospray tandem mass spectrometry: a tool for the diagnosis of sialic acid storage diseaseFredoen Valianpour, Nicolaas G G M Abeling, Marinus Duran, et al.
Pediatric Research|March 21, 2003
Characteristic acylcarnitine profiles in inherited defects of peroxisome biogenesis: a novel tool for screening diagnosis using tandem mass spectrometryCristiano Rizzo, Sara Boenzi, Ronald J A Wanders, et al.
European Journal of Pediatrics|October 16, 2007
Fasting adaptation in idiopathic ketotic hypoglycemia: a mismatch between glucose production and demandHidde H Huidekoper, Marinus Duran, Marjolein Turkenburg, et al.
Pediatric Research|December 3, 2009
Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiencyBianca T van Maldegem, Marinus Duran, Ronald J A Wanders, et al.
The Biochemical Journal|January 22, 2003
L-serine in disease and developmentTom J de Koning, Keith Snell, Marinus Duran, et al.
AJNR. American Journal of Neuroradiology|January 20, 2004
Neonatal citrullinemia: comparison of conventional MR, diffusion-weighted, and diffusion tensor findingsCharles B L M Majoie, Jeroen M Mourmans, Erik M Akkerman, et al.
American Journal of Human Genetics|November 16, 2002
3-Methylglutaconic aciduria type I is caused by mutations in AUHLodewijk IJlst, Ference J Loupatty, Jos P N Ruiter, et al.
Pageof 8