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H Ogier

Showing results (41-50 of 127) with videos related to

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Journal of Inherited Metabolic Disease|October 13, 2009
Mitochondria and diabetes mellitus: untangling a conflictive relationship?M Schiff, S Loublier, A Coulibaly, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Hyperammonemia secondary to hereditary organic acidurias: a study of 29 casesJ M Saudubray, F X Coudé, H Ogier, et al.
Pediatric Research|January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosisF X Coude, H Ogier, A Munnich, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|October 2, 2007
[Mitochondrial neurogastrointestinal encephalomyopathy]P Rousset, M Elmaleh-Bergès, H Ogier de Baulny, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Enzymatic and immunological demonstration of normal and defective succinic semialdehyde dehydrogenase activity in fetal brain, liver and kidneyK L Chambliss, C F Lee, H Ogier, et al.
Lancet (London, England)|May 14, 1983
Antenatal diagnosis of glutaricaciduria type IIG Mitchell, J M Saudubray, Y Benoit, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Diagnosis of carnitine acylcarnitine translocase deficiency by complementation analysisM Brivet, A Slama, H Ogier, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1984
[Type II oculo-cutaneous tyrosinosis]N Gounod, H Ogier, J L Dufier, et al.
The Journal of Pediatrics|November 1, 1995
Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocaseH Ogier de Baulny, A Slama, G Touati, et al.
Progress in Clinical and Biological Research|January 1, 1982
Acute and long-term management of infants with aminoacidopathies and organic aciduriasJ M Saudubray, H Ogier, C Charpentier, et al.
Pageof 13

Showing results (41-50 of 127) with videos related to

Sort By:
Pageof 13
Journal of Inherited Metabolic Disease|October 13, 2009
Mitochondria and diabetes mellitus: untangling a conflictive relationship?M Schiff, S Loublier, A Coulibaly, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Hyperammonemia secondary to hereditary organic acidurias: a study of 29 casesJ M Saudubray, F X Coudé, H Ogier, et al.
Pediatric Research|January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosisF X Coude, H Ogier, A Munnich, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|October 2, 2007
[Mitochondrial neurogastrointestinal encephalomyopathy]P Rousset, M Elmaleh-Bergès, H Ogier de Baulny, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Enzymatic and immunological demonstration of normal and defective succinic semialdehyde dehydrogenase activity in fetal brain, liver and kidneyK L Chambliss, C F Lee, H Ogier, et al.
Lancet (London, England)|May 14, 1983
Antenatal diagnosis of glutaricaciduria type IIG Mitchell, J M Saudubray, Y Benoit, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Diagnosis of carnitine acylcarnitine translocase deficiency by complementation analysisM Brivet, A Slama, H Ogier, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1984
[Type II oculo-cutaneous tyrosinosis]N Gounod, H Ogier, J L Dufier, et al.
The Journal of Pediatrics|November 1, 1995
Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocaseH Ogier de Baulny, A Slama, G Touati, et al.
Progress in Clinical and Biological Research|January 1, 1982
Acute and long-term management of infants with aminoacidopathies and organic aciduriasJ M Saudubray, H Ogier, C Charpentier, et al.
Pageof 13