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D Ketting

Showing results (41-50 of 55) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1975
Permanent chemical phenylketonuria and a normal phenylalanine tolerance in two sisters with a normal mental developmentS K Wadman, D Ketting, P K De Bree, et al.
Journal of Chromatography|February 13, 1981
Determination of the absolute configuration of some biologically important urinary 2-hydroxydicarboxylic acids by capillary gas--liquid chromatographyJ P Kamerling, M Duran, G J Gerwig, et al.
Pediatric Research|October 1, 1977
Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated musclesJ P Van Biervliet, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1977
(2-Ethoxyethoxy)acetic acid: an unusual compound found in the gas chromatographic analysis of urinary organic acidsJ P Kamerling, M Duran, L Bruinvis, et al.
Pediatric Research|January 1, 1992
Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementationM Duran, C B Cleutjens, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1975
Tyrosinemia and tyrosyluria in healthy prematures: time courses not vitamin C-dependentH D Bakker, S K Wadman, F J Van Sprang, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Identification of the stereoisomeric configurations of methylcitric acid produced by si-citrate synthase and methylcitrate synthase using capillary gas chromatography-mass spectrometryJ P van Rooyen, L J Mienie, E Erasmus, et al.
European Journal of Pediatrics|January 18, 1979
Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levelsH Przyrembel, H J Bremer, M Duran, et al.
European Journal of Pediatrics|January 1, 1991
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatmentM Duran, R J Wanders, J P de Jager, et al.
European Journal of Pediatrics|July 1, 1981
A case of formiminoglutamic aciduria. Clinical and biochemical studiesM Duran, D Ketting, P K de Bree, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1975
Permanent chemical phenylketonuria and a normal phenylalanine tolerance in two sisters with a normal mental developmentS K Wadman, D Ketting, P K De Bree, et al.
Journal of Chromatography|February 13, 1981
Determination of the absolute configuration of some biologically important urinary 2-hydroxydicarboxylic acids by capillary gas--liquid chromatographyJ P Kamerling, M Duran, G J Gerwig, et al.
Pediatric Research|October 1, 1977
Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated musclesJ P Van Biervliet, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1977
(2-Ethoxyethoxy)acetic acid: an unusual compound found in the gas chromatographic analysis of urinary organic acidsJ P Kamerling, M Duran, L Bruinvis, et al.
Pediatric Research|January 1, 1992
Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementationM Duran, C B Cleutjens, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1975
Tyrosinemia and tyrosyluria in healthy prematures: time courses not vitamin C-dependentH D Bakker, S K Wadman, F J Van Sprang, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Identification of the stereoisomeric configurations of methylcitric acid produced by si-citrate synthase and methylcitrate synthase using capillary gas chromatography-mass spectrometryJ P van Rooyen, L J Mienie, E Erasmus, et al.
European Journal of Pediatrics|January 18, 1979
Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levelsH Przyrembel, H J Bremer, M Duran, et al.
European Journal of Pediatrics|January 1, 1991
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatmentM Duran, R J Wanders, J P de Jager, et al.
European Journal of Pediatrics|July 1, 1981
A case of formiminoglutamic aciduria. Clinical and biochemical studiesM Duran, D Ketting, P K de Bree, et al.
Pageof 6