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P Divry

Showing results (31-40 of 114) with videos related to

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Archives Francaises De Pediatrie|June 1, 1973
[A case of isovaleric acidemia]P Guibaud, P Divry, Y Dubois, et al.
La Revue De Medecine Interne|March 1, 1988
[Neurological complications of lymphography. Apropos of a case]T Marsepoil, P Levesque, M Bertaux, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Stable-isotope selected-ion monitoring quantification of methylmalonic acid in dried filter-paper urine samplesJ M Parnet, P Divry, C Vianey-Saban, et al.
European Journal of Pediatrics|August 1, 1992
Prenatal diagnosis of Canavan diseaseC Jakobs, H J ten Brink, P Divry, et al.
Nephrologie|January 1, 1994
[Molecular pathology of type 1 primary hyperoxaluria]P Cochat, M O Rolland, D Bozon, et al.
Biology of the Neonate|January 1, 1987
Ketogenesis in hypoglycemic neonates. Carnitine and dicarboxylic acids in neonatal hypoglycemiaL Sann, P Divry, B Cartier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblastsC Bertrand, R Dumoulin, P Divry, et al.
Journal of Inherited Metabolic Disease|August 7, 2001
Mevalonic aciduria and hyper-IgD syndrome: two sides of the same coin?M Tsimaratos, I Kone-Paut, P Divry, et al.
Pediatrie|April 1, 1980
[Vitamin B 12 responsive methylmalenic aciduria. Apropos of a new case]L Sann, P Divry, M O Rolland, et al.
European Journal of Pediatrics|September 1, 1984
Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduriaK M Gibson, L Sweetman, W L Nyhan, et al.
Pageof 12

Showing results (31-40 of 114) with videos related to

Sort By:
Pageof 12
Archives Francaises De Pediatrie|June 1, 1973
[A case of isovaleric acidemia]P Guibaud, P Divry, Y Dubois, et al.
La Revue De Medecine Interne|March 1, 1988
[Neurological complications of lymphography. Apropos of a case]T Marsepoil, P Levesque, M Bertaux, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Stable-isotope selected-ion monitoring quantification of methylmalonic acid in dried filter-paper urine samplesJ M Parnet, P Divry, C Vianey-Saban, et al.
European Journal of Pediatrics|August 1, 1992
Prenatal diagnosis of Canavan diseaseC Jakobs, H J ten Brink, P Divry, et al.
Nephrologie|January 1, 1994
[Molecular pathology of type 1 primary hyperoxaluria]P Cochat, M O Rolland, D Bozon, et al.
Biology of the Neonate|January 1, 1987
Ketogenesis in hypoglycemic neonates. Carnitine and dicarboxylic acids in neonatal hypoglycemiaL Sann, P Divry, B Cartier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblastsC Bertrand, R Dumoulin, P Divry, et al.
Journal of Inherited Metabolic Disease|August 7, 2001
Mevalonic aciduria and hyper-IgD syndrome: two sides of the same coin?M Tsimaratos, I Kone-Paut, P Divry, et al.
Pediatrie|April 1, 1980
[Vitamin B 12 responsive methylmalenic aciduria. Apropos of a new case]L Sann, P Divry, M O Rolland, et al.
European Journal of Pediatrics|September 1, 1984
Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduriaK M Gibson, L Sweetman, W L Nyhan, et al.
Pageof 12