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J M Trijbels

Showing results (51-60 of 177) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1987
Localization of pipecolic acid metabolism in rat liver peroxisomes: probable explanation for hyperpipecolataemia in Zellweger syndromeJ M Trijbels, L A Monnens, G Melis, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Cerebrospinal fluid homocysteine and the cobalamin status of the brainH J Blom, R A Wevers, A Verrips, et al.
Biochimica Et Biophysica Acta|February 19, 1988
Acyl-CoA oxidase activity and peroxisomal fatty acid oxidation in rat tissuesF A Reubsaet, J H Veerkamp, S G Bukkens, et al.
Metabolism: Clinical and Experimental|June 1, 1989
Cystathionine-synthase-deficient patients do not use the transamination pathway of methionine to reduce hypermethioninemia and homocystinemiaH J Blom, G H Boers, J M Trijbels, et al.
Early Human Development|September 1, 1979
Experimental intrauterine growth retardation in the rat. Evaluation of the Wigglesworth modelL A Kollée, L A Monnens, J M Trijbels, et al.
The International Journal of Biochemistry|January 1, 1984
Chemical composition and solubility of human glomerular and tubular basement membranes of adult and senescent menJ P Langeveld, J H Veerkamp, J M Trijbels, et al.
European Journal of Pediatrics|May 1, 1988
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activityW Sperl, W Ruitenbeek, J M Trijbels, et al.
European Journal of Pediatrics|March 1, 1981
alpha-Aminoadipic aciduria and persistence of fetal haemoglobin in an oligophrenic childA J Manders, C G von Oostrom, J M Trijbels, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1977
L-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retinaJ M Trijbels, R C Sengers, J A Bakkeren, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 12, 1973
Propionic acid, an artefact which can leave methylmalonic acidemia undiscoveredM Duran, D Ketting, S K Wadman, et al.
Pageof 18

Showing results (51-60 of 177) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|January 1, 1987
Localization of pipecolic acid metabolism in rat liver peroxisomes: probable explanation for hyperpipecolataemia in Zellweger syndromeJ M Trijbels, L A Monnens, G Melis, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Cerebrospinal fluid homocysteine and the cobalamin status of the brainH J Blom, R A Wevers, A Verrips, et al.
Biochimica Et Biophysica Acta|February 19, 1988
Acyl-CoA oxidase activity and peroxisomal fatty acid oxidation in rat tissuesF A Reubsaet, J H Veerkamp, S G Bukkens, et al.
Metabolism: Clinical and Experimental|June 1, 1989
Cystathionine-synthase-deficient patients do not use the transamination pathway of methionine to reduce hypermethioninemia and homocystinemiaH J Blom, G H Boers, J M Trijbels, et al.
Early Human Development|September 1, 1979
Experimental intrauterine growth retardation in the rat. Evaluation of the Wigglesworth modelL A Kollée, L A Monnens, J M Trijbels, et al.
The International Journal of Biochemistry|January 1, 1984
Chemical composition and solubility of human glomerular and tubular basement membranes of adult and senescent menJ P Langeveld, J H Veerkamp, J M Trijbels, et al.
European Journal of Pediatrics|May 1, 1988
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activityW Sperl, W Ruitenbeek, J M Trijbels, et al.
European Journal of Pediatrics|March 1, 1981
alpha-Aminoadipic aciduria and persistence of fetal haemoglobin in an oligophrenic childA J Manders, C G von Oostrom, J M Trijbels, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1977
L-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retinaJ M Trijbels, R C Sengers, J A Bakkeren, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 12, 1973
Propionic acid, an artefact which can leave methylmalonic acidemia undiscoveredM Duran, D Ketting, S K Wadman, et al.
Pageof 18