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Daniel Rabier

Showing results (1-10 of 34) with videos related to

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The Journal of Nutrition|May 22, 2007
Biomarkers identified in inborn errors for lysine, arginine, and ornithineJean-Marie Saudubray, Daniel Rabier
European Journal of Pediatrics|May 17, 2002
A risk factor for chronic mild hyperammonaemiaPierre Kamoun, Daniel Rabier, Jean-Marie Saudubray
Archives of Neurology|February 16, 2011
Validation of plasma branched chain amino acids as biomarkers in Huntington diseaseFanny Mochel, Sandra Benaich, Daniel Rabier, et al.
Metabolism: Clinical and Experimental|December 15, 2007
L-arginine metabolism in dog kidney and isolated nephron segmentsOlivier Levillain, Daniel Rabier, Bernard Duclos, et al.
Pediatric Research|August 9, 2005
Kinetic modeling of plasma leucine levels during continuous venovenous extracorporeal removal therapy in neonates with maple syrup urine diseasePhilippe Jouvet, Philippe Hubert, Jean Marie Saudubray, et al.
Biochimica Et Biophysica Acta|December 7, 2007
Modified glutamine catabolism in macrophages of Ucp2 knock-out miceTobias Nübel, Yalin Emre, Daniel Rabier, et al.
Sleep|September 21, 2005
Effect of genetically caused excess of brain gamma-hydroxybutyric acid and GABA on sleepIsabelle Arnulf, Eric Konofal, K Michael Gibson, et al.
Annals of Neurology|November 10, 2005
Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspectsAngels García-Cazorla, Daniel Rabier, Guy Touati, et al.
Molecular Genetics and Metabolism|March 23, 2005
Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapyFanny Mochel, Pascale DeLonlay, Guy Touati, et al.
The Journal of Pediatrics|August 31, 2006
Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patientsAngels Garcia-Cazorla, Pascale De Lonlay, Pierre Rustin, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
The Journal of Nutrition|May 22, 2007
Biomarkers identified in inborn errors for lysine, arginine, and ornithineJean-Marie Saudubray, Daniel Rabier
European Journal of Pediatrics|May 17, 2002
A risk factor for chronic mild hyperammonaemiaPierre Kamoun, Daniel Rabier, Jean-Marie Saudubray
Archives of Neurology|February 16, 2011
Validation of plasma branched chain amino acids as biomarkers in Huntington diseaseFanny Mochel, Sandra Benaich, Daniel Rabier, et al.
Metabolism: Clinical and Experimental|December 15, 2007
L-arginine metabolism in dog kidney and isolated nephron segmentsOlivier Levillain, Daniel Rabier, Bernard Duclos, et al.
Pediatric Research|August 9, 2005
Kinetic modeling of plasma leucine levels during continuous venovenous extracorporeal removal therapy in neonates with maple syrup urine diseasePhilippe Jouvet, Philippe Hubert, Jean Marie Saudubray, et al.
Biochimica Et Biophysica Acta|December 7, 2007
Modified glutamine catabolism in macrophages of Ucp2 knock-out miceTobias Nübel, Yalin Emre, Daniel Rabier, et al.
Sleep|September 21, 2005
Effect of genetically caused excess of brain gamma-hydroxybutyric acid and GABA on sleepIsabelle Arnulf, Eric Konofal, K Michael Gibson, et al.
Annals of Neurology|November 10, 2005
Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspectsAngels García-Cazorla, Daniel Rabier, Guy Touati, et al.
Molecular Genetics and Metabolism|March 23, 2005
Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapyFanny Mochel, Pascale DeLonlay, Guy Touati, et al.
The Journal of Pediatrics|August 31, 2006
Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patientsAngels Garcia-Cazorla, Pascale De Lonlay, Pierre Rustin, et al.
Pageof 4