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Showing results (41-50 of 127) with videos related to

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Journal of Lipid Research|October 1, 1992
Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disordersH J ten Brink, D S Schor, R M Kok, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Muscle strength in children with medium-chain acyl-CoA dehydrogenase deficiencyJ W Custers, B T Poll-The, M Duran, et al.
European Journal of Pediatrics|December 29, 2000
Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiencyT J de Koning, M Duran, L Dorland, et al.
AJNR. American Journal of Neuroradiology|January 19, 2006
Sequential MR imaging changes in nonketotic hyperglycinemiaJ Mourmans, C B L M Majoie, P G Barth, et al.
Biochimica Et Biophysica Acta|April 12, 1996
Non-rhizomelic and rhizomelic chondrodysplasia punctata within a single complementation groupA M Motley, H F Tabak, J A Smeitink, et al.
Clinical Chemistry|March 25, 1998
Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid beta-oxidation disordersC G Costa, L Dorland, U Holwerda, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Cerebrospinal fluid organic acids in biotinidase deficiencyM Duran, E R Baumgartner, T M Suormala, et al.
Lancet (London, England)|June 19, 1993
Sudden infant death associated with defective oxidative phosphorylationJ A Smeitink, J C Fischer, W Ruitenbeek, et al.
Pediatric Research|November 1, 1994
Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiencyA J Bergman, R A Donckerwolcke, M Duran, et al.
Journal of Inherited Metabolic Disease|December 16, 2000
Hyperketonaemia in glycerol kinase deficiencyD R Sjarif, L Dorland, W Sperl, et al.
Pageof 13

Showing results (41-50 of 127) with videos related to

Sort By:
Pageof 13
Journal of Lipid Research|October 1, 1992
Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disordersH J ten Brink, D S Schor, R M Kok, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Muscle strength in children with medium-chain acyl-CoA dehydrogenase deficiencyJ W Custers, B T Poll-The, M Duran, et al.
European Journal of Pediatrics|December 29, 2000
Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiencyT J de Koning, M Duran, L Dorland, et al.
AJNR. American Journal of Neuroradiology|January 19, 2006
Sequential MR imaging changes in nonketotic hyperglycinemiaJ Mourmans, C B L M Majoie, P G Barth, et al.
Biochimica Et Biophysica Acta|April 12, 1996
Non-rhizomelic and rhizomelic chondrodysplasia punctata within a single complementation groupA M Motley, H F Tabak, J A Smeitink, et al.
Clinical Chemistry|March 25, 1998
Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid beta-oxidation disordersC G Costa, L Dorland, U Holwerda, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Cerebrospinal fluid organic acids in biotinidase deficiencyM Duran, E R Baumgartner, T M Suormala, et al.
Lancet (London, England)|June 19, 1993
Sudden infant death associated with defective oxidative phosphorylationJ A Smeitink, J C Fischer, W Ruitenbeek, et al.
Pediatric Research|November 1, 1994
Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiencyA J Bergman, R A Donckerwolcke, M Duran, et al.
Journal of Inherited Metabolic Disease|December 16, 2000
Hyperketonaemia in glycerol kinase deficiencyD R Sjarif, L Dorland, W Sperl, et al.
Pageof 13