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D Rabier

Showing results (111-120 of 157) with videos related to

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The Journal of Clinical Investigation|June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiencyT Bourgeron, D Chretien, J Poggi-Bach, et al.
Transplantation Proceedings|February 1, 1994
Liver transplantation: new indications in metabolic disorders?D Jan, F Poggi, J Laurent, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation in urea cycle disordersJ M Saudubray, G Touati, P Delonlay, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Familial encephalopathy and L-2-hydroxyglutaric aciduriaN Kaabachi, A Larnaout, D Rabier, et al.
European Journal of Pediatrics|March 1, 1994
Liver cytochrome c oxidase deficiency in a case of neonatal-onset hepatic failureP Edery, B Gérard, D Chretien, et al.
Progress in Clinical and Biological Research|January 1, 1992
Approach to the patient with a fatty acid oxidation disorderJ M Saudubray, G Mitchell, J P Bonnefont, et al.
The Journal of Pediatrics|August 1, 1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosisJ P Bonnefont, D Chretien, P Rustin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1994
[Diagnosis of metabolic coma in children]F Poggi-Travert, B Héron, T Billette de Villemeur, et al.
The Journal of Pediatrics|December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onsetV Cormier, P Rustin, J P Bonnefont, et al.
Journal of Medical Genetics|July 1, 1992
Site specific screening for point mutations in ornithine transcarbamylase deficiencyD Feldmann, J M Rozet, A Pelet, et al.
Pageof 16

Showing results (111-120 of 157) with videos related to

Sort By:
Pageof 16
The Journal of Clinical Investigation|June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiencyT Bourgeron, D Chretien, J Poggi-Bach, et al.
Transplantation Proceedings|February 1, 1994
Liver transplantation: new indications in metabolic disorders?D Jan, F Poggi, J Laurent, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation in urea cycle disordersJ M Saudubray, G Touati, P Delonlay, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Familial encephalopathy and L-2-hydroxyglutaric aciduriaN Kaabachi, A Larnaout, D Rabier, et al.
European Journal of Pediatrics|March 1, 1994
Liver cytochrome c oxidase deficiency in a case of neonatal-onset hepatic failureP Edery, B Gérard, D Chretien, et al.
Progress in Clinical and Biological Research|January 1, 1992
Approach to the patient with a fatty acid oxidation disorderJ M Saudubray, G Mitchell, J P Bonnefont, et al.
The Journal of Pediatrics|August 1, 1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosisJ P Bonnefont, D Chretien, P Rustin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1994
[Diagnosis of metabolic coma in children]F Poggi-Travert, B Héron, T Billette de Villemeur, et al.
The Journal of Pediatrics|December 1, 1991
Hepatic failure in disorders of oxidative phosphorylation with neonatal onsetV Cormier, P Rustin, J P Bonnefont, et al.
Journal of Medical Genetics|July 1, 1992
Site specific screening for point mutations in ornithine transcarbamylase deficiencyD Feldmann, J M Rozet, A Pelet, et al.
Pageof 16