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Journal of Inherited Metabolic Disease
|
November 25, 2010
Enzymology of the branched-chain amino acid oxidation disorders: the valine pathway
Ronald 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 adrenoleukodystrophy
Robert-Jan Sanders, Rob Ofman, Marinus Duran, et al.
BMJ Case Reports
|
June 29, 2011
Neonatal carnitine palmitoyltransferase II deficiency: failure of treatment despite prolonged survival
Petra 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 disease
Fredoen 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 spectrometry
Cristiano 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 demand
Hidde 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 deficiency
Bianca T van Maldegem, Marinus Duran, Ronald J A Wanders, et al.
The Biochemical Journal
|
January 22, 2003
L-serine in disease and development
Tom 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 findings
Charles 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 AUH
Lodewijk IJlst, Ference J Loupatty, Jos P N Ruiter, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 72) with videos related to
Sort By:
Page
of 8
Journal of Inherited Metabolic Disease
|
November 25, 2010
Enzymology of the branched-chain amino acid oxidation disorders: the valine pathway
Ronald 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 adrenoleukodystrophy
Robert-Jan Sanders, Rob Ofman, Marinus Duran, et al.
BMJ Case Reports
|
June 29, 2011
Neonatal carnitine palmitoyltransferase II deficiency: failure of treatment despite prolonged survival
Petra 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 disease
Fredoen 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 spectrometry
Cristiano 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 demand
Hidde 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 deficiency
Bianca T van Maldegem, Marinus Duran, Ronald J A Wanders, et al.
The Biochemical Journal
|
January 22, 2003
L-serine in disease and development
Tom 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 findings
Charles 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 AUH
Lodewijk IJlst, Ference J Loupatty, Jos P N Ruiter, et al.
Page
of 8