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Dominique Loiseau

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

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The International Journal of Biochemistry & Cell Biology|April 25, 2009
OPA1-associated disorders: phenotypes and pathophysiologyPatrizia Amati-Bonneau, Dan Milea, Dominique Bonneau, et al.
BMC Research Notes|December 24, 2011
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respirationClaire Angebault, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Annals of Neurology|April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A diseaseDominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Annals of Neurology|May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defectArnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
Annals of Neurology|March 25, 2008
Reversible optic neuropathy with OPA1 exon 5b mutationKaren Cornille, Dan Milea, Patrizia Amati-Bonneau, et al.
Genome Research|October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distributionGhizlane Elachouri, Sara Vidoni, Claudia Zanna, 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.
The International Journal of Biochemistry & Cell Biology|April 25, 2009
OPA1-associated disorders: phenotypes and pathophysiologyPatrizia Amati-Bonneau, Dan Milea, Dominique Bonneau, et al.
BMC Research Notes|December 24, 2011
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respirationClaire Angebault, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Annals of Neurology|April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A diseaseDominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Annals of Neurology|May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defectArnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
Annals of Neurology|March 25, 2008
Reversible optic neuropathy with OPA1 exon 5b mutationKaren Cornille, Dan Milea, Patrizia Amati-Bonneau, et al.
Genome Research|October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distributionGhizlane Elachouri, Sara Vidoni, Claudia Zanna, et al.
Pageof 2