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D Ketting

Showing results (11-20 of 55) with videos related to

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Pediatric Research|May 1, 1987
D-glyceric acidemia: an inborn error associated with fructose metabolismM Duran, F A Beemer, L Bruinvis, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Urinary D-4-hydroxyphenyllactate, D-phenyllactate and D-2-hydroxyisocaproate, abnormalities of bacterial originL J Spaapen, D Ketting, S K Wadman, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Direct identification of propionylcarnitine in propionic acidaemia: biochemical and clinical results of oral carnitine supplementationM Duran, D Ketting, T E Beckeringh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 1, 1971
Urinary and faecal excretion of metabolites of tyrosine and phenylalanine in a patient with cystic fibrosis and severely impaired amino acid absorptionC Van der Heiden, S K Wadman, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 8, 1980
3-methyl-3-butenoic acid: an artefact in the urinary metabolic pattern of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyC Jakobs, M Bojasch, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1978
The absolute configuration of urinary 2-hydroxybutyric acid in patients with ketosis and lactic acidosisJ P Kamerling, G J Gerwig, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1983
Isovalerylglucuronide, a new urinary metabolite in isovaleric acidemia. Identification problems due to rearrangement reactionsL Dorland, M Duran, S K Wadman, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
The differential diagnosis of dicarboxylic aciduriaM Duran, J B De Klerk, S K Wadman, et al.
Clinical Chemistry|March 1, 1988
Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiencyM Duran, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1971
Gas chromatographic analysis of urinary tyrosine and phenylalanine metabolites in patients with gastrointestinal disordersC van der Heiden, E A Wauters, M Duran, et al.
Pageof 6

Showing results (11-20 of 55) with videos related to

Sort By:
Pageof 6
Pediatric Research|May 1, 1987
D-glyceric acidemia: an inborn error associated with fructose metabolismM Duran, F A Beemer, L Bruinvis, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Urinary D-4-hydroxyphenyllactate, D-phenyllactate and D-2-hydroxyisocaproate, abnormalities of bacterial originL J Spaapen, D Ketting, S K Wadman, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Direct identification of propionylcarnitine in propionic acidaemia: biochemical and clinical results of oral carnitine supplementationM Duran, D Ketting, T E Beckeringh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 1, 1971
Urinary and faecal excretion of metabolites of tyrosine and phenylalanine in a patient with cystic fibrosis and severely impaired amino acid absorptionC Van der Heiden, S K Wadman, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 8, 1980
3-methyl-3-butenoic acid: an artefact in the urinary metabolic pattern of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyC Jakobs, M Bojasch, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1978
The absolute configuration of urinary 2-hydroxybutyric acid in patients with ketosis and lactic acidosisJ P Kamerling, G J Gerwig, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1983
Isovalerylglucuronide, a new urinary metabolite in isovaleric acidemia. Identification problems due to rearrangement reactionsL Dorland, M Duran, S K Wadman, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
The differential diagnosis of dicarboxylic aciduriaM Duran, J B De Klerk, S K Wadman, et al.
Clinical Chemistry|March 1, 1988
Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiencyM Duran, L Bruinvis, D Ketting, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1971
Gas chromatographic analysis of urinary tyrosine and phenylalanine metabolites in patients with gastrointestinal disordersC van der Heiden, E A Wauters, M Duran, et al.
Pageof 6