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C Jakobs

Showing results (111-120 of 417) with videos related to

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Human Genomics|January 24, 2009
Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiencyPatrizia Malaspina, Matthew J Picklo, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Bile acids in amniotic fluid: promising metabolites for the prenatal diagnosis of peroxisomal disordersF Stellaard, W J Kleijer, R J Wanders, et al.
Prenatal Diagnosis|March 1, 1996
A case of tyrosinaemia type I with normal level of succinylacetone in the amniotic fluidA Grenier, S Cederbaum, C Laberge, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overviewR Castro, I Rivera, H J Blom, et al.
European Journal of Clinical Investigation|March 27, 1999
Neurone-specific enolase and N-acetyl-aspartate as potential peripheral markers of ischaemic strokeH Stevens, C Jakobs, A E de Jager, et al.
Kidney International|January 20, 1999
Plasma homocysteine concentration predicts mortality in non-insulin-dependent diabetic patients with and without albuminuriaC D Stehouwer, M A Gall, P Hougaard, et al.
European Journal of Pediatrics|July 1, 1985
Prenatal diagnosis of tyrosinaemia type I by use of stable isotope dilution mass spectrometryC Jakobs, E A Kvittingen, R Berger, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Renal failure in adult patients with hereditary tyrosinaemia type IE A Kvittingen, T Talseth, S Halvorsen, et al.
Acta Chirurgiae Orthopaedicae Et Traumatologiae Cechoslovaca|April 24, 2014
Lower limb salvage: indication and decision making for replantation, revascularisation and amputationS Märdian, K D Schaser, F Wichlas, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Major hyperpipecolataemia in a normal adultC Vallat, S Denis, H Bellet, et al.
Pageof 42

Showing results (111-120 of 417) with videos related to

Sort By:
Pageof 42
Human Genomics|January 24, 2009
Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiencyPatrizia Malaspina, Matthew J Picklo, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Bile acids in amniotic fluid: promising metabolites for the prenatal diagnosis of peroxisomal disordersF Stellaard, W J Kleijer, R J Wanders, et al.
Prenatal Diagnosis|March 1, 1996
A case of tyrosinaemia type I with normal level of succinylacetone in the amniotic fluidA Grenier, S Cederbaum, C Laberge, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overviewR Castro, I Rivera, H J Blom, et al.
European Journal of Clinical Investigation|March 27, 1999
Neurone-specific enolase and N-acetyl-aspartate as potential peripheral markers of ischaemic strokeH Stevens, C Jakobs, A E de Jager, et al.
Kidney International|January 20, 1999
Plasma homocysteine concentration predicts mortality in non-insulin-dependent diabetic patients with and without albuminuriaC D Stehouwer, M A Gall, P Hougaard, et al.
European Journal of Pediatrics|July 1, 1985
Prenatal diagnosis of tyrosinaemia type I by use of stable isotope dilution mass spectrometryC Jakobs, E A Kvittingen, R Berger, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Renal failure in adult patients with hereditary tyrosinaemia type IE A Kvittingen, T Talseth, S Halvorsen, et al.
Acta Chirurgiae Orthopaedicae Et Traumatologiae Cechoslovaca|April 24, 2014
Lower limb salvage: indication and decision making for replantation, revascularisation and amputationS Märdian, K D Schaser, F Wichlas, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Major hyperpipecolataemia in a normal adultC Vallat, S Denis, H Bellet, et al.
Pageof 42