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Marinus Duran

Showing results (31-40 of 72) with videos related to

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Clinical Science (London, England : 1979)|October 24, 2008
Muscle acylcarnitines during short-term fasting in lean healthy menMaarten R Soeters, Hans P Sauerwein, Marinus Duran, et al.
Molecular Genetics and Metabolism|April 20, 2006
High incidence of hyperoxaluria in generalized peroxisomal disordersChristiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.
Journal of Hepatology|December 15, 2010
New insights on the mechanisms of valproate-induced hyperammonemia: inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoACátia C P Aires, Arno van Cruchten, Lodewijk Ijlst, et al.
Epilepsia|January 19, 2006
Beta-ureidopropionase deficiency presenting with febrile status epilepticusBirgit E Assmann, Andre B P Van Kuilenburg, Felix Distelmaier, et al.
Molecular Genetics and Metabolism|April 3, 2004
Spastic diplegia and periventricular white matter abnormalities in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, a defect of isoleucine metabolism: differential diagnosis with hypoxic-ischemic brain diseasesBwee Tien Poll-The, Ronald J A Wanders, Jos P N Ruiter, et al.
Clinical Chemistry|January 21, 2006
Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB geneAnibh M Das, Sabine Illsinger, Thomas Lücke, et al.
JAMA|August 24, 2006
Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiencyBianca T van Maldegem, Marinus Duran, Ronald J A Wanders, et al.
Biochemical Pharmacology|October 27, 2009
Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosisCátia C P Aires, Lodewijk Ijlst, Femke Stet, et al.
Plos One|May 26, 2010
Plasma and erythrocyte fatty acid patterns in patients with recurrent depression: a matched case-control studyJohanna Assies, François Pouwer, Anja Lok, et al.
Journal of Inherited Metabolic Disease|December 23, 2011
Inhibition of 3-methylcrotonyl-CoA carboxylase explains the increased excretion of 3-hydroxyisovaleric acid in valproate-treated patientsPaula B M Luís, Jos P Ruiter, Lodewijk IJlst, et al.
Pageof 8

Showing results (31-40 of 72) with videos related to

Sort By:
Pageof 8
Clinical Science (London, England : 1979)|October 24, 2008
Muscle acylcarnitines during short-term fasting in lean healthy menMaarten R Soeters, Hans P Sauerwein, Marinus Duran, et al.
Molecular Genetics and Metabolism|April 20, 2006
High incidence of hyperoxaluria in generalized peroxisomal disordersChristiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.
Journal of Hepatology|December 15, 2010
New insights on the mechanisms of valproate-induced hyperammonemia: inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoACátia C P Aires, Arno van Cruchten, Lodewijk Ijlst, et al.
Epilepsia|January 19, 2006
Beta-ureidopropionase deficiency presenting with febrile status epilepticusBirgit E Assmann, Andre B P Van Kuilenburg, Felix Distelmaier, et al.
Molecular Genetics and Metabolism|April 3, 2004
Spastic diplegia and periventricular white matter abnormalities in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, a defect of isoleucine metabolism: differential diagnosis with hypoxic-ischemic brain diseasesBwee Tien Poll-The, Ronald J A Wanders, Jos P N Ruiter, et al.
Clinical Chemistry|January 21, 2006
Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB geneAnibh M Das, Sabine Illsinger, Thomas Lücke, et al.
JAMA|August 24, 2006
Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiencyBianca T van Maldegem, Marinus Duran, Ronald J A Wanders, et al.
Biochemical Pharmacology|October 27, 2009
Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosisCátia C P Aires, Lodewijk Ijlst, Femke Stet, et al.
Plos One|May 26, 2010
Plasma and erythrocyte fatty acid patterns in patients with recurrent depression: a matched case-control studyJohanna Assies, François Pouwer, Anja Lok, et al.
Journal of Inherited Metabolic Disease|December 23, 2011
Inhibition of 3-methylcrotonyl-CoA carboxylase explains the increased excretion of 3-hydroxyisovaleric acid in valproate-treated patientsPaula B M Luís, Jos P Ruiter, Lodewijk IJlst, et al.
Pageof 8