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P Divry

Showing results (71-80 of 114) with videos related to

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Journal of Inherited Metabolic Disease|July 15, 2000
Antenatal expression of multiple acyl-CoA dehydrogenase deficiencyC Vianey-Saban, R Bouvier, P Cochat, et al.
Archives Francaises De Pediatrie|June 1, 1993
[Generalized epilepsy disclosing medium-chain-acyl-CoA dehydrogenase deficiency]B Chabrol, J Mancini, C Bertrand, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 16-month-old childM O Rolland, P Divry, M T Zabot, et al.
Pediatrie|January 1, 1993
[Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings]N Guffon, C Vianey-Saban, J C Berthier, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Early prenatal diagnosis of propionic acidaemia with simultaneous sampling of chorionic villus and amniotic fluidM O Rolland, P Divry, G Mandon, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. III. Enzymology and inheritanceK M Gibson, I Jansen, L Sweetman, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
5-Oxoprolinuria (glutathione synthetase deficiency): a case with neonatal presentation and rapid fatal outcomeP Divry, F Roulaud-Parrot, C Dorche, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1998
Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patientsC Vianey-Saban, P Divry, M Brivet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 1983
A new patient with 4-hydroxybutyric aciduria, a possible defect of 4-aminobutyrate metabolismP Divry, P Baltassat, M O Rolland, et al.
Pediatrie|January 1, 1989
[Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin]L de Parscau, B Beaufrère, C Vianey-Liaud, et al.
Pageof 12

Showing results (71-80 of 114) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|July 15, 2000
Antenatal expression of multiple acyl-CoA dehydrogenase deficiencyC Vianey-Saban, R Bouvier, P Cochat, et al.
Archives Francaises De Pediatrie|June 1, 1993
[Generalized epilepsy disclosing medium-chain-acyl-CoA dehydrogenase deficiency]B Chabrol, J Mancini, C Bertrand, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 16-month-old childM O Rolland, P Divry, M T Zabot, et al.
Pediatrie|January 1, 1993
[Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings]N Guffon, C Vianey-Saban, J C Berthier, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Early prenatal diagnosis of propionic acidaemia with simultaneous sampling of chorionic villus and amniotic fluidM O Rolland, P Divry, G Mandon, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. III. Enzymology and inheritanceK M Gibson, I Jansen, L Sweetman, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
5-Oxoprolinuria (glutathione synthetase deficiency): a case with neonatal presentation and rapid fatal outcomeP Divry, F Roulaud-Parrot, C Dorche, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1998
Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patientsC Vianey-Saban, P Divry, M Brivet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 1983
A new patient with 4-hydroxybutyric aciduria, a possible defect of 4-aminobutyrate metabolismP Divry, P Baltassat, M O Rolland, et al.
Pediatrie|January 1, 1989
[Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin]L de Parscau, B Beaufrère, C Vianey-Liaud, et al.
Pageof 12