Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Amati-Bonneau

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
Revue Neurologique|June 1, 2005
[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs]C Verny, P Amati-Bonneau, F Dubas, et al.
Revue Neurologique|May 7, 2014
Mitochondrial dysfunction affecting visual pathwaysS Leruez, P Amati-Bonneau, C Verny, et al.
Clinical Genetics|December 25, 2004
Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1P Amati-Bonneau, L Pasquier, E Lainey, et al.
Journal Francais D'Ophtalmologie|February 24, 2007
[A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothers]R Macarez, P Amati-Bonneau, X Burelle, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
Revue Neurologique|May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondriaV Procaccio, C Bris, J M Chao de la Barca, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Revue Neurologique|June 1, 2005
[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs]C Verny, P Amati-Bonneau, F Dubas, et al.
Revue Neurologique|May 7, 2014
Mitochondrial dysfunction affecting visual pathwaysS Leruez, P Amati-Bonneau, C Verny, et al.
Clinical Genetics|December 25, 2004
Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1P Amati-Bonneau, L Pasquier, E Lainey, et al.
Journal Francais D'Ophtalmologie|February 24, 2007
[A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothers]R Macarez, P Amati-Bonneau, X Burelle, et al.
Revue Neurologique|November 9, 2010
[Hereditary optic atrophies]C Scherer, V Procaccio, M Ferre, et al.
Revue Neurologique|May 6, 2014
Perspectives of drug-based neuroprotection targeting mitochondriaV Procaccio, C Bris, J M Chao de la Barca, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Pageof 2