Search research articles
Contact Us
Filters
Showing results (41-50 of 91) with videos related to
Page
of 10
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]
J M Pinard, C Marsac, E Barkaoui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 1, 1983
Biotin dependent carboxylase activities in normal human and multicarboxylase deficient patient fibroblasts: relationship to the biotin content of the culture medium
C Marsac, M Gaudry, C Augereau, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutation
F Degoul, M Diry, D Rodriguez, et al.
Annals of Neurology
|
June 1, 1991
Zidovudine myopathy: a distinctive disorder associated with mitochondrial dysfunction
C Mhiri, M Baudrimont, G Bonne, et al.
Muscle & Nerve
|
November 1, 1995
Myasthenic symptoms in patients with mitochondrial myopathies
N Le Forestier, R K Gherardi, C Meyrignac, et al.
American Journal of Human Genetics
|
January 1, 1987
The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe
B H Robinson, J Oei, J M Saudubray, et al.
Human Molecular Genetics
|
April 18, 1998
Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle gene
F Degoul, H Brulé, C Cepanec, et al.
Free Radical Research
|
November 8, 2001
UV-A irradiation induces a decrease in the mitochondrial respiratory activity of human NCTC 2544 keratinocytes
M Djavaheri-Mergny, C Marsac, C Mazière, et al.
Neuropediatrics
|
November 5, 2003
Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation
I Desguerre, F Pinton, R Nabbout, et al.
Revue Neurologique
|
January 1, 1991
[Familial mitochondrial encephalopathy. A clinicopathologic study]
B Estournet, C Duyckaerts, C Marsac, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 91) with videos related to
Sort By:
Page
of 10
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]
J M Pinard, C Marsac, E Barkaoui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 1, 1983
Biotin dependent carboxylase activities in normal human and multicarboxylase deficient patient fibroblasts: relationship to the biotin content of the culture medium
C Marsac, M Gaudry, C Augereau, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutation
F Degoul, M Diry, D Rodriguez, et al.
Annals of Neurology
|
June 1, 1991
Zidovudine myopathy: a distinctive disorder associated with mitochondrial dysfunction
C Mhiri, M Baudrimont, G Bonne, et al.
Muscle & Nerve
|
November 1, 1995
Myasthenic symptoms in patients with mitochondrial myopathies
N Le Forestier, R K Gherardi, C Meyrignac, et al.
American Journal of Human Genetics
|
January 1, 1987
The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe
B H Robinson, J Oei, J M Saudubray, et al.
Human Molecular Genetics
|
April 18, 1998
Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle gene
F Degoul, H Brulé, C Cepanec, et al.
Free Radical Research
|
November 8, 2001
UV-A irradiation induces a decrease in the mitochondrial respiratory activity of human NCTC 2544 keratinocytes
M Djavaheri-Mergny, C Marsac, C Mazière, et al.
Neuropediatrics
|
November 5, 2003
Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation
I Desguerre, F Pinton, R Nabbout, et al.
Revue Neurologique
|
January 1, 1991
[Familial mitochondrial encephalopathy. A clinicopathologic study]
B Estournet, C Duyckaerts, C Marsac, et al.
Page
of 10