M Duran|S K Wadman - JoVE Visualize

Showing results (11-20 of 551) with videos related to

Pageof 56

Sort By:

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.

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, 1984

The differential diagnosis of dicarboxylic aciduriaM Duran, J B De Klerk, S K Wadman, et al.

Advances in Experimental Medicine and Biology|January 1, 1986

Detection of inherited adenylosuccinase deficiency by two dimensional thin layer chromatography of urinary imidazolesS K Wadman, P K de Bree, M Duran, 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|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|May 15, 1986

Diagnosis of inherited adenylosuccinase deficiency by thin-layer chromatography of urinary imidazoles and by automated cation exchange column chromatography of purinesP K de Bree, S K Wadman, M Duran, et al.

Pediatrics|December 1, 1986

Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiencyM Duran, M Hofkamp, W J Rhead, 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.

Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987

Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolismM Duran, D Ketting, L Bruinvis, et al.

Pageof 56

Showing results (11-20 of 551) with videos related to

Sort By:

Pageof 56

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.

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, 1984

The differential diagnosis of dicarboxylic aciduriaM Duran, J B De Klerk, S K Wadman, et al.

Advances in Experimental Medicine and Biology|January 1, 1986

Detection of inherited adenylosuccinase deficiency by two dimensional thin layer chromatography of urinary imidazolesS K Wadman, P K de Bree, M Duran, 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|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|May 15, 1986

Diagnosis of inherited adenylosuccinase deficiency by thin-layer chromatography of urinary imidazoles and by automated cation exchange column chromatography of purinesP K de Bree, S K Wadman, M Duran, et al.

Pediatrics|December 1, 1986

Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiencyM Duran, M Hofkamp, W J Rhead, 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.

Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987

Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolismM Duran, D Ketting, L Bruinvis, et al.

Pageof 56