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R J Wanders

Showing results (431-440 of 497) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
A patient with lethal cardiomyopathy and a carnitine-acylcarnitine translocase deficiencyK E Niezen-Koning, F J van Spronsen, L Ijlst, et al.
European Journal of Biochemistry|July 8, 1998
Carnitine palmitoyltransferase II specificity towards beta-oxidation intermediates--evidence for a reverse carnitine cycle in mitochondriaF V Ventura, L Ijlst, J Ruiter, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel dataD De Craemer, M J Zweens, S Lyonnet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1987
Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndromeR J Wanders, W Smit, H S Heymans, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblastsR J Wanders, C W van Roermund, M J van Wijland, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfallR J Soorani-Lunsing, F J van Spronsen, I Stolte-Dijkstra, et al.
Hepatology (Baltimore, Md.)|August 1, 1995
Peroxisome mosaicism in the livers of peroxisomal deficiency patientsM Espeel, H Mandel, F Poggi, et al.
The Journal of Clinical Investigation|December 1, 1987
Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disordersR J Wanders, C W van Roermund, M J van Wijland, et al.
Brain : a Journal of Neurology|June 16, 2001
Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndromeM A Willemsen, L IJlst, P M Steijlen, et al.
Experimental Cell Research|May 1, 1987
Peroxisomes and peroxisomal functions in muscle. Studies with muscle cells from controls and a patient with the cerebro-hepato-renal (Zellweger) syndromeR J Wanders, P G Barth, C W van Roermund, et al.
Pageof 50

Showing results (431-440 of 497) with videos related to

Sort By:
Pageof 50
Journal of Inherited Metabolic Disease|January 1, 1995
A patient with lethal cardiomyopathy and a carnitine-acylcarnitine translocase deficiencyK E Niezen-Koning, F J van Spronsen, L Ijlst, et al.
European Journal of Biochemistry|July 8, 1998
Carnitine palmitoyltransferase II specificity towards beta-oxidation intermediates--evidence for a reverse carnitine cycle in mitochondriaF V Ventura, L Ijlst, J Ruiter, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel dataD De Craemer, M J Zweens, S Lyonnet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1987
Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndromeR J Wanders, W Smit, H S Heymans, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblastsR J Wanders, C W van Roermund, M J van Wijland, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfallR J Soorani-Lunsing, F J van Spronsen, I Stolte-Dijkstra, et al.
Hepatology (Baltimore, Md.)|August 1, 1995
Peroxisome mosaicism in the livers of peroxisomal deficiency patientsM Espeel, H Mandel, F Poggi, et al.
The Journal of Clinical Investigation|December 1, 1987
Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disordersR J Wanders, C W van Roermund, M J van Wijland, et al.
Brain : a Journal of Neurology|June 16, 2001
Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndromeM A Willemsen, L IJlst, P M Steijlen, et al.
Experimental Cell Research|May 1, 1987
Peroxisomes and peroxisomal functions in muscle. Studies with muscle cells from controls and a patient with the cerebro-hepato-renal (Zellweger) syndromeR J Wanders, P G Barth, C W van Roermund, et al.
Pageof 50