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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 cases
J M Saudubray, F X Coudé, H Ogier, et al.
Pediatric Research
|
January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosis
F 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 kidney
K L Chambliss, C F Lee, H Ogier, et al.
Lancet (London, England)
|
May 14, 1983
Antenatal diagnosis of glutaricaciduria type II
G Mitchell, J M Saudubray, Y Benoit, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Diagnosis of carnitine acylcarnitine translocase deficiency by complementation analysis
M 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 translocase
H 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 acidurias
J M Saudubray, H Ogier, C Charpentier, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 127) with videos related to
Sort By:
Page
of 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 cases
J M Saudubray, F X Coudé, H Ogier, et al.
Pediatric Research
|
January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosis
F 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 kidney
K L Chambliss, C F Lee, H Ogier, et al.
Lancet (London, England)
|
May 14, 1983
Antenatal diagnosis of glutaricaciduria type II
G Mitchell, J M Saudubray, Y Benoit, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Diagnosis of carnitine acylcarnitine translocase deficiency by complementation analysis
M 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 translocase
H 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 acidurias
J M Saudubray, H Ogier, C Charpentier, et al.
Page
of 13