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Showing results (31-40 of 169) with videos related to

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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.
American Journal of Physiology. Cell Physiology|May 15, 2001
Protease-activated receptor-2-mediated inhibition of ion transport in human bronchial epithelial cellsH Danahay, L Withey, C T Poll, 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.
American Journal of Physiology. Cell Physiology|October 3, 2003
Niflumic acid inhibits ATP-stimulated exocytosis in a mucin-secreting epithelial cell lineC A Bertrand, H Danahay, C T Poll, 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.
JIMD Reports|August 13, 2016
The Challenges of a Successful Pregnancy in a Patient with Adult Refsum's Disease due to Phytanoyl-CoA Hydroxylase DeficiencyKarolina M Stepien, Anthony S Wierzbicki, Bwee T Poll-The, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Peroxisomal disorders: a reviewB Fournier, J A Smeitink, L Dorland, et al.
Human Genetics|January 1, 1989
Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disordersB T Poll-The, O H Skjeldal, O Stokke, et al.
Biology of the Neonate|January 1, 1990
Clinical approach to inherited metabolic disorders in neonatesJ M Saudubray, C Narcy, L Lyonnet, et al.
Pageof 17

Showing results (31-40 of 169) with videos related to

Sort By:
Pageof 17
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.
American Journal of Physiology. Cell Physiology|May 15, 2001
Protease-activated receptor-2-mediated inhibition of ion transport in human bronchial epithelial cellsH Danahay, L Withey, C T Poll, 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.
American Journal of Physiology. Cell Physiology|October 3, 2003
Niflumic acid inhibits ATP-stimulated exocytosis in a mucin-secreting epithelial cell lineC A Bertrand, H Danahay, C T Poll, 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.
JIMD Reports|August 13, 2016
The Challenges of a Successful Pregnancy in a Patient with Adult Refsum's Disease due to Phytanoyl-CoA Hydroxylase DeficiencyKarolina M Stepien, Anthony S Wierzbicki, Bwee T Poll-The, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Peroxisomal disorders: a reviewB Fournier, J A Smeitink, L Dorland, et al.
Human Genetics|January 1, 1989
Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disordersB T Poll-The, O H Skjeldal, O Stokke, et al.
Biology of the Neonate|January 1, 1990
Clinical approach to inherited metabolic disorders in neonatesJ M Saudubray, C Narcy, L Lyonnet, et al.
Pageof 17