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R J Wanders

Showing results (341-350 of 497) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1991
A new type of chondrodysplasia punctata associated with peroxisomal dysfunctionB T Poll-The, P Maroteaux, C Narcy, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Broad specificity of carnitine palmitoyltransferase II towards long-chain acyl-CoA beta-oxidation intermediates and its practical approach to the synthesis of various long-chain acylcarnitinesF V Ventura, C G Costa, L IJlst, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Rapid analysis of conjugated bile acids in plasma using electrospray tandem mass spectrometry: application for selective screening of peroxisomal disordersA H Bootsma, H Overmars, A van Rooij, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Progressive generalized brain atrophy and infantile spasms associated with cytochrome c oxidase deficiencyH D Bakker, C Van den Bogert, J G Drewes, et al.
Pediatric Research|September 27, 2000
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1A Imamura, N Shimozawa, Y Suzuki, et al.
European Journal of Pediatrics|March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcomeE Lopriore, R J Gemke, N M Verhoeven, et al.
Journal of Lipid Research|July 1, 1985
Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndromeG Schrakamp, C F Roosenboom, R B Schutgens, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1993
Peroxisomal beta-oxidation of polyunsaturated long chain fatty acids in human fibroblasts. The polyunsaturated and the saturated long chain fatty acids are retroconverted by the same acyl-CoA oxidaseE Christensen, B Woldseth, T A Hagve, et al.
Biochemical Society Transactions|May 18, 2001
Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseasesR J Wanders, P Vreken, S Ferdinandusse, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Prenatal diagnosis of systemic disorders of the respiratory chain in cultured amniocytes and chorionic villus fibroblasts by studying the formation of lactate and pyruvate from glucoseR J Wanders, F A Wijburg, J Ruiter, et al.
Pageof 50

Showing results (341-350 of 497) with videos related to

Sort By:
Pageof 50
Journal of Inherited Metabolic Disease|January 1, 1991
A new type of chondrodysplasia punctata associated with peroxisomal dysfunctionB T Poll-The, P Maroteaux, C Narcy, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Broad specificity of carnitine palmitoyltransferase II towards long-chain acyl-CoA beta-oxidation intermediates and its practical approach to the synthesis of various long-chain acylcarnitinesF V Ventura, C G Costa, L IJlst, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Rapid analysis of conjugated bile acids in plasma using electrospray tandem mass spectrometry: application for selective screening of peroxisomal disordersA H Bootsma, H Overmars, A van Rooij, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Progressive generalized brain atrophy and infantile spasms associated with cytochrome c oxidase deficiencyH D Bakker, C Van den Bogert, J G Drewes, et al.
Pediatric Research|September 27, 2000
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1A Imamura, N Shimozawa, Y Suzuki, et al.
European Journal of Pediatrics|March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcomeE Lopriore, R J Gemke, N M Verhoeven, et al.
Journal of Lipid Research|July 1, 1985
Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndromeG Schrakamp, C F Roosenboom, R B Schutgens, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1993
Peroxisomal beta-oxidation of polyunsaturated long chain fatty acids in human fibroblasts. The polyunsaturated and the saturated long chain fatty acids are retroconverted by the same acyl-CoA oxidaseE Christensen, B Woldseth, T A Hagve, et al.
Biochemical Society Transactions|May 18, 2001
Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseasesR J Wanders, P Vreken, S Ferdinandusse, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Prenatal diagnosis of systemic disorders of the respiratory chain in cultured amniocytes and chorionic villus fibroblasts by studying the formation of lactate and pyruvate from glucoseR J Wanders, F A Wijburg, J Ruiter, et al.
Pageof 50