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F Demaugre

Showing results (21-30 of 46) with videos related to

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The Journal of Clinical Investigation|March 1, 1993
Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblastsS V Pande, M Brivet, A Slama, 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|January 1, 1992
Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiencyC A Stanley, F Sunaryo, D E Hale, 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.
Pediatric Research|May 1, 1990
Immunoquantitative analysis of human carnitine palmitoyltransferase I and II defectsF Demaugre, J P Bonnefont, C Cepanec, et al.
The New England Journal of Medicine|December 14, 1978
Dichloroacetate as treatment for congenital lactic acidosisF X Coude, J M Saudubray, F DeMaugre, et al.
The Journal of Clinical Investigation|March 1, 1991
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficienciesF Demaugre, J P Bonnefont, M Colonna, et al.
Biochemical Society Transactions|July 3, 1998
Inborn errors of metabolism in the light of metabolic control analysisJ P Mazat, T Letellier, M Malgat, et al.
Pediatric Research|October 1, 1982
Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidationJ M Saudubray, F X Coudé, F Demaugre, et al.
European Journal of Biochemistry|October 1, 1992
Evidence for an impaired long-chain fatty acid oxidation and ketogenesis in Fao hepatoma cellsC Prip-Buus, A C Bouthillier-Voisin, C Kohl, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
The Journal of Clinical Investigation|March 1, 1993
Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblastsS V Pande, M Brivet, A Slama, 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|January 1, 1992
Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiencyC A Stanley, F Sunaryo, D E Hale, 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.
Pediatric Research|May 1, 1990
Immunoquantitative analysis of human carnitine palmitoyltransferase I and II defectsF Demaugre, J P Bonnefont, C Cepanec, et al.
The New England Journal of Medicine|December 14, 1978
Dichloroacetate as treatment for congenital lactic acidosisF X Coude, J M Saudubray, F DeMaugre, et al.
The Journal of Clinical Investigation|March 1, 1991
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficienciesF Demaugre, J P Bonnefont, M Colonna, et al.
Biochemical Society Transactions|July 3, 1998
Inborn errors of metabolism in the light of metabolic control analysisJ P Mazat, T Letellier, M Malgat, et al.
Pediatric Research|October 1, 1982
Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidationJ M Saudubray, F X Coudé, F Demaugre, et al.
European Journal of Biochemistry|October 1, 1992
Evidence for an impaired long-chain fatty acid oxidation and ketogenesis in Fao hepatoma cellsC Prip-Buus, A C Bouthillier-Voisin, C Kohl, et al.
Pageof 5