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Biochimica Et Biophysica Acta|May 8, 1992
Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liverR J Wanders, S Denis, C W van Roermund, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysisN M Verhoeven, C Jakobs, H J ten Brink, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
Lactic acidosis in long-chain fatty acid beta-oxidation disordersF V Ventura, J P Ruiter, L IJlst, et al.
European Journal of Pediatrics|October 1, 1994
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorderA C Sewell, S W Bender, S Wirth, et al.
Journal of Leukocyte Biology|April 1, 2018
Downregulated eosinophil activity in ulcerative colitis with concomitant primary sclerosing cholangitisMaria Lampinen, Annika Fredricsson, Johan Vessby, et al.
Journal of Inherited Metabolic Disease|March 5, 2016
The important role of biochemical and functional studies in the diagnostics of peroxisomal disordersSacha Ferdinandusse, Merel S Ebberink, Frédéric M Vaz, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
3-Hydroxy-2-methylbutyryl-CoA dehydrogenase deficiencyV R Sutton, W E O'Brien, G D Clark, et al.
Molecular Genetics and Metabolism|July 12, 2015
Metabolite studies in HIBCH and ECHS1 defects: Implications for screeningHeidi Peters, Sacha Ferdinandusse, Jos P Ruiter, et al.
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