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H Carchon

Showing results (11-20 of 17) with videos related to

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Archives of Disease in Childhood|June 1, 1996
3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesisJ Jaeken, M Detheux, L Van Maldergem, et al.
Age and Ageing|May 1, 1984
Positive 14CO2 bile acid breath test in elderly peopleJ Hellemans, E Joosten, Y Ghoos, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)R Barone, H Carchon, E Jansen, et al.
The Journal of Clinical Investigation|August 26, 1998
A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharideP Burda, L Borsig, J de Rijk-van Andel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 22, 2007
Clinical and biochemical features in a Congolese infant with congenital disorder of glycosylation (CDG)-IIxN C Nsibu, J Jaeken, H Carchon, et al.
The Journal of Biological Chemistry|October 28, 1994
Peroxisomal beta-oxidation. Purification of four novel 3-hydroxyacyl-CoA dehydrogenases from rat liver peroxisomesD K Novikov, G F Vanhove, H Carchon, et al.
Lipids|June 1, 2001
Oxidative catabolism of alpha-tocopherol in rat liver microsomesH Van Houte, E De Hoffmann, P P Van Veldhoven, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Archives of Disease in Childhood|June 1, 1996
3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesisJ Jaeken, M Detheux, L Van Maldergem, et al.
Age and Ageing|May 1, 1984
Positive 14CO2 bile acid breath test in elderly peopleJ Hellemans, E Joosten, Y Ghoos, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)R Barone, H Carchon, E Jansen, et al.
The Journal of Clinical Investigation|August 26, 1998
A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharideP Burda, L Borsig, J de Rijk-van Andel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 22, 2007
Clinical and biochemical features in a Congolese infant with congenital disorder of glycosylation (CDG)-IIxN C Nsibu, J Jaeken, H Carchon, et al.
The Journal of Biological Chemistry|October 28, 1994
Peroxisomal beta-oxidation. Purification of four novel 3-hydroxyacyl-CoA dehydrogenases from rat liver peroxisomesD K Novikov, G F Vanhove, H Carchon, et al.
Lipids|June 1, 2001
Oxidative catabolism of alpha-tocopherol in rat liver microsomesH Van Houte, E De Hoffmann, P P Van Veldhoven, et al.
Pageof 2