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P Divry

Showing results (81-90 of 114) with videos related to

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Acta Paediatrica Scandinavica|November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhoodP Divry, M David, N Gregersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1996
Acylcarnitine removal in a patient with acyl-CoA beta-oxidation deficiency disorder: effect of L-carnitine therapy and starvationM Fontaine, G Briand, L Vallée, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 10, 1998
Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiencyM Fontaine, G Briand, C Largillière, et al.
Annales De Pediatrie|November 1, 1987
[Hypertrophic cardiomyopathy and neonatal encephalopathy associated with 3-methylglutaconic aciduria]J C Netter, P Divry, B Delisle, et al.
Pediatrie|December 1, 1984
[Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency]J P Collet, P Divry, J F Blanc, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Lethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyE Martins, A Costa, E Silva, et al.
Archives of Disease in Childhood|December 22, 2000
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiencyE H Touma, M S Rashed, C Vianey-Saban, et al.
Pediatrie|December 1, 1977
[Abetalipoproteinemia. Clinical, genetic, endocrine and metabolic study of a recent familial case]J P Feit, M David, V Macabéo, et al.
Lancet (London, England)|May 20, 1989
Liver transplantation in primary hyperoxaluria type 1P Cochat, J L Faure, P Divry, et al.
Annales De Pediatrie|November 1, 1986
[Combined sulfite and xanthine oxidase deficiency due to an anomaly in the metabolism of molybdenum cofactor]P Lagier, J M Tessonnier, S Collet, et al.
Pageof 12

Showing results (81-90 of 114) with videos related to

Sort By:
Pageof 12
Acta Paediatrica Scandinavica|November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhoodP Divry, M David, N Gregersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1996
Acylcarnitine removal in a patient with acyl-CoA beta-oxidation deficiency disorder: effect of L-carnitine therapy and starvationM Fontaine, G Briand, L Vallée, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 10, 1998
Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiencyM Fontaine, G Briand, C Largillière, et al.
Annales De Pediatrie|November 1, 1987
[Hypertrophic cardiomyopathy and neonatal encephalopathy associated with 3-methylglutaconic aciduria]J C Netter, P Divry, B Delisle, et al.
Pediatrie|December 1, 1984
[Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency]J P Collet, P Divry, J F Blanc, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Lethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyE Martins, A Costa, E Silva, et al.
Archives of Disease in Childhood|December 22, 2000
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiencyE H Touma, M S Rashed, C Vianey-Saban, et al.
Pediatrie|December 1, 1977
[Abetalipoproteinemia. Clinical, genetic, endocrine and metabolic study of a recent familial case]J P Feit, M David, V Macabéo, et al.
Lancet (London, England)|May 20, 1989
Liver transplantation in primary hyperoxaluria type 1P Cochat, J L Faure, P Divry, et al.
Annales De Pediatrie|November 1, 1986
[Combined sulfite and xanthine oxidase deficiency due to an anomaly in the metabolism of molybdenum cofactor]P Lagier, J M Tessonnier, S Collet, et al.
Pageof 12