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Journal of Lipid Research|February 4, 2003
A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiencyJolein Gloerich, Simone Denis, Elisabeth G van Grunsven, et al.
Biochimica Et Biophysica Acta|December 17, 2013
A role for the human peroxisomal half-transporter ABCD3 in the oxidation of dicarboxylic acidsCarlo W T van Roermund, Lodewijk Ijlst, Tom Wagemans, et al.
International Journal of Methods in Psychiatric Research|May 22, 2015
What does the beck depression inventory measure in myocardial infarction patients? a psychometric approach using item response theory and person-fitKlaas J Wardenaar, Rob B K Wanders, Annelieke M Roest, et al.
Biochimie|January 1, 1993
Postnatal diagnosis of peroxisomal disorders: a biochemical approachR J Wanders, R B Schutgens, P G Barth, et al.
Biochimica Et Biophysica Acta|December 16, 2014
Enzymatic characterization of ELOVL1, a key enzyme in very long-chain fatty acid synthesisMartin J A Schackmann, Rob Ofman, Inge M E Dijkstra, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 23, 2007
Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiencyS A Thompson, J Calvin, S Hogg, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidaseH J ten Brink, B T Poll-The, J M Saudubray, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 6, 2000
Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycleW Röschinger, A C Muntau, M Duran, et al.
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