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B T Poll-The

Showing results (11-20 of 127) with videos related to

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Lancet (London, England)|May 22, 1993
Phenylpyruvate, fetal damage, and maternal phenylketonuria syndromeL Dorland, B T Poll-The, M Duran, et al.
Lancet (London, England)|September 28, 1996
Maternal 3-methylglutaconic aciduria associated with abnormalities in offspringT j de Koning, M Duran, L Dorland, et al.
European Journal of Pediatrics|April 1, 1994
Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiencyR P Beekman, N Hofstee, J A Smeitink, et al.
Progress in Clinical and Biological Research|January 1, 1990
Complementation analysis of peroxisomal disorders and classical RefsumB T Poll-The, O H Skjeldal, O Stokke, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
The metabolism of phytanic acid and pristanic acid in man: a reviewN M Verhoeven, R J Wanders, B T Poll-The, et al.
Pediatric Research|October 6, 1999
Dynamic changes of plasma acylcarnitine levels induced by fasting and sunflower oil challenge test in childrenC C Costa, I T de Almeida, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Medium-chain triglyceride loading has no diagnostic power in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyC G Costa, I T de Almeida, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Plasma total odd-chain fatty acids in the monitoring of disorders of propionate, methylmalonate and biotin metabolismM Coker, J B de Klerk, B T Poll-The, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidaseH J ten Brink, B T Poll-The, J M Saudubray, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Peroxisomal disorders: a reviewB Fournier, J A Smeitink, L Dorland, et al.
Pageof 13

Showing results (11-20 of 127) with videos related to

Sort By:
Pageof 13
Lancet (London, England)|May 22, 1993
Phenylpyruvate, fetal damage, and maternal phenylketonuria syndromeL Dorland, B T Poll-The, M Duran, et al.
Lancet (London, England)|September 28, 1996
Maternal 3-methylglutaconic aciduria associated with abnormalities in offspringT j de Koning, M Duran, L Dorland, et al.
European Journal of Pediatrics|April 1, 1994
Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiencyR P Beekman, N Hofstee, J A Smeitink, et al.
Progress in Clinical and Biological Research|January 1, 1990
Complementation analysis of peroxisomal disorders and classical RefsumB T Poll-The, O H Skjeldal, O Stokke, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
The metabolism of phytanic acid and pristanic acid in man: a reviewN M Verhoeven, R J Wanders, B T Poll-The, et al.
Pediatric Research|October 6, 1999
Dynamic changes of plasma acylcarnitine levels induced by fasting and sunflower oil challenge test in childrenC C Costa, I T de Almeida, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Medium-chain triglyceride loading has no diagnostic power in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyC G Costa, I T de Almeida, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Plasma total odd-chain fatty acids in the monitoring of disorders of propionate, methylmalonate and biotin metabolismM Coker, J B de Klerk, B T Poll-The, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidaseH J ten Brink, B T Poll-The, J M Saudubray, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Peroxisomal disorders: a reviewB Fournier, J A Smeitink, L Dorland, et al.
Pageof 13