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R J Wanders

Showing results (411-420 of 497) with videos related to

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Journal of the Neurological Sciences|April 1, 1988
Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's diseaseR J Wanders, H S Heymans, R B Schutgens, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.
Journal of Lipid Research|August 1, 1997
Lipoprotein[a] is not present in the plasma of patients with some peroxisomal disordersY Y van der Hoek, R J Wanders, A E van den Ende, et al.
Pediatric Research|August 6, 2000
Heterozygosity for the common LCHAD mutation (1528g>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is lowM E den Boer, L Ijlst, F A Wijburg, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disordersR J Wanders, M J van Wijland, C W van Roermund, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresisJ A Smeitink, F A Beemer, M Espeel, et al.
Human Molecular Genetics|May 20, 1999
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disordersN Shimozawa, Y Suzuki, Z Zhang, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Adenine nucleotide translocator deficiency in muscle: potential therapeutic value of vitamin EH D Bakker, H R Scholte, C Van den Bogert, et al.
Analytical Biochemistry|February 22, 2001
Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolitesM F Silva, J P Ruiter, L IJlst, et al.
Pediatric Research|January 7, 2000
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancyA M Innes, L E Seargeant, K Balachandra, et al.
Pageof 50

Showing results (411-420 of 497) with videos related to

Sort By:
Pageof 50
Journal of the Neurological Sciences|April 1, 1988
Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's diseaseR J Wanders, H S Heymans, R B Schutgens, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.
Journal of Lipid Research|August 1, 1997
Lipoprotein[a] is not present in the plasma of patients with some peroxisomal disordersY Y van der Hoek, R J Wanders, A E van den Ende, et al.
Pediatric Research|August 6, 2000
Heterozygosity for the common LCHAD mutation (1528g>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is lowM E den Boer, L Ijlst, F A Wijburg, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disordersR J Wanders, M J van Wijland, C W van Roermund, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresisJ A Smeitink, F A Beemer, M Espeel, et al.
Human Molecular Genetics|May 20, 1999
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disordersN Shimozawa, Y Suzuki, Z Zhang, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Adenine nucleotide translocator deficiency in muscle: potential therapeutic value of vitamin EH D Bakker, H R Scholte, C Van den Bogert, et al.
Analytical Biochemistry|February 22, 2001
Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolitesM F Silva, J P Ruiter, L IJlst, et al.
Pediatric Research|January 7, 2000
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancyA M Innes, L E Seargeant, K Balachandra, et al.
Pageof 50