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J M Collombet

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Journal of Neuroscience Research|September 1, 1996
Time course and regional expression of C-FOS and HSP70 in hippocampus and piriform cortex following soman-induced seizuresV Baille-Le Crom, J M Collombet, M F Burckhart, et al.
Molecular and Cellular Biochemistry|March 1, 1997
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathiesJ M Collombet, H Faure-Vigny, G Mandon, et al.
Acta Neurologica Scandinavica|June 1, 1995
An abnormal exercise test response revealing a respiratory chain complex III deficiencyB Mousson, J M Collombet, R Dumoulin, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new caseN Guffon, C Lopez-Mediavilla, R Dumoulin, et al.
Neuroreport|December 29, 1995
Early regional changes of GFAP mRNA in rat hippocampus and dentate gyrus during soman-induced seizuresV Baille-Le Crom, J M Collombet, P Carpentier, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Journal of Neuroscience Research|September 1, 1996
Time course and regional expression of C-FOS and HSP70 in hippocampus and piriform cortex following soman-induced seizuresV Baille-Le Crom, J M Collombet, M F Burckhart, et al.
Molecular and Cellular Biochemistry|March 1, 1997
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathiesJ M Collombet, H Faure-Vigny, G Mandon, et al.
Acta Neurologica Scandinavica|June 1, 1995
An abnormal exercise test response revealing a respiratory chain complex III deficiencyB Mousson, J M Collombet, R Dumoulin, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new caseN Guffon, C Lopez-Mediavilla, R Dumoulin, et al.
Neuroreport|December 29, 1995
Early regional changes of GFAP mRNA in rat hippocampus and dentate gyrus during soman-induced seizuresV Baille-Le Crom, J M Collombet, P Carpentier, et al.
Pageof 2