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D Rabier

Showing results (41-50 of 157) with videos related to

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Clinical Chemistry|January 1, 1989
A new pitfall in plasma amino acid analysisP Parvy, J Bardet, D Rabier, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Alloisoleucine in isovaleric acidaemiaD Rabier, P Parvy, J Bardet, et al.
The Biochemical Journal|October 15, 1983
Inhibition of ureagenesis by valproate in rat hepatocytes. Role of N-acetylglutamate and acetyl-CoAF X Coude, G Grimber, P Parvy, et al.
Journal of Inherited Metabolic Disease|May 4, 2005
Urea cycle defects: management and outcomeM C Nassogne, B Héron, G Touati, et al.
The Biochemical Journal|September 15, 1982
Acute effects of glucagon on citrulline biosynthesisD Rabier, P Briand, F Petit, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 25, 1998
Lethal ornithine transcarbamylase deficiency in a female neonate: a new caseS Klosowski, C Largilliere, L Storme, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Differing clinical presentation of succinic semialdehyde dehydrogenase deficiency in adolescent siblings from Lifu Island, New CaledoniaK M Gibson, A E Doskey, D Rabier, et al.
Human Genetics|December 1, 1991
Fatal hyperammonemia resulting from a C-to-T mutation at a MspI site of the ornithine transcarbamylase geneD Hentzen, A Pelet, D Feldman, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Ornithine carbamoyltransferase deficiency with subnormal enzyme activityD Rabier, B Guillois, J Bardet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 1, 1994
[Protocol of metabolic investigations in hereditary metabolic diseases]F Poggi, D Rabier, A Vassault, et al.
Pageof 16

Showing results (41-50 of 157) with videos related to

Sort By:
Pageof 16
Clinical Chemistry|January 1, 1989
A new pitfall in plasma amino acid analysisP Parvy, J Bardet, D Rabier, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Alloisoleucine in isovaleric acidaemiaD Rabier, P Parvy, J Bardet, et al.
The Biochemical Journal|October 15, 1983
Inhibition of ureagenesis by valproate in rat hepatocytes. Role of N-acetylglutamate and acetyl-CoAF X Coude, G Grimber, P Parvy, et al.
Journal of Inherited Metabolic Disease|May 4, 2005
Urea cycle defects: management and outcomeM C Nassogne, B Héron, G Touati, et al.
The Biochemical Journal|September 15, 1982
Acute effects of glucagon on citrulline biosynthesisD Rabier, P Briand, F Petit, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 25, 1998
Lethal ornithine transcarbamylase deficiency in a female neonate: a new caseS Klosowski, C Largilliere, L Storme, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Differing clinical presentation of succinic semialdehyde dehydrogenase deficiency in adolescent siblings from Lifu Island, New CaledoniaK M Gibson, A E Doskey, D Rabier, et al.
Human Genetics|December 1, 1991
Fatal hyperammonemia resulting from a C-to-T mutation at a MspI site of the ornithine transcarbamylase geneD Hentzen, A Pelet, D Feldman, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Ornithine carbamoyltransferase deficiency with subnormal enzyme activityD Rabier, B Guillois, J Bardet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 1, 1994
[Protocol of metabolic investigations in hereditary metabolic diseases]F Poggi, D Rabier, A Vassault, et al.
Pageof 16