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

Christophe Verny

Showing results (41-50 of 92) with videos related to

Pageof 10
Sort By:
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Ocular Immunology and Inflammation|January 23, 2025
Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic PresentationLaurie Mourozeau, Virginie Pichon, Aymane Bouzidi, et al.
Mitochondrion|July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutationChristophe Verny, Naig Guegen, Valerie Desquiret, et al.
Brain : a Journal of Neurology|November 1, 2022
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probandsAude Rocatcher, Valérie Desquiret-Dumas, Majida Charif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathyCédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Neuroimage. Clinical|March 1, 2020
Neocortical morphometry in Huntington's disease: Indication of the coexistence of abnormal neurodevelopmental and neurodegenerative processesJean-Francois Mangin, Denis Rivière, Edouard Duchesnay, et al.
Neurogenetics|April 29, 2014
Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcificationGaël Nicolas, Anne-Claire Richard, Cyril Pottier, et al.
Parkinsonism & Related Disorders|September 27, 2025
Comparison of tetrabenazine, tiapride and olanzapine in Huntington's disease: a one-year French randomized multicenter study (Neuro-HD)Katia Youssov, Etienne Audureau, Jérémie Pariente, et al.
Neuropsychologia|June 10, 2011
The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's diseasePhilippe Allain, Véronique Gaura, Luciano Fasotti, et al.
Journal of Medical Genetics|January 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformationsFrançoise Bergametti, Geraldine Viot, Christophe Verny, et al.
Pageof 10

Showing results (41-50 of 92) with videos related to

Sort By:
Pageof 10
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Ocular Immunology and Inflammation|January 23, 2025
Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic PresentationLaurie Mourozeau, Virginie Pichon, Aymane Bouzidi, et al.
Mitochondrion|July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutationChristophe Verny, Naig Guegen, Valerie Desquiret, et al.
Brain : a Journal of Neurology|November 1, 2022
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probandsAude Rocatcher, Valérie Desquiret-Dumas, Majida Charif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathyCédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Neuroimage. Clinical|March 1, 2020
Neocortical morphometry in Huntington's disease: Indication of the coexistence of abnormal neurodevelopmental and neurodegenerative processesJean-Francois Mangin, Denis Rivière, Edouard Duchesnay, et al.
Neurogenetics|April 29, 2014
Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcificationGaël Nicolas, Anne-Claire Richard, Cyril Pottier, et al.
Parkinsonism & Related Disorders|September 27, 2025
Comparison of tetrabenazine, tiapride and olanzapine in Huntington's disease: a one-year French randomized multicenter study (Neuro-HD)Katia Youssov, Etienne Audureau, Jérémie Pariente, et al.
Neuropsychologia|June 10, 2011
The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's diseasePhilippe Allain, Véronique Gaura, Luciano Fasotti, et al.
Journal of Medical Genetics|January 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformationsFrançoise Bergametti, Geraldine Viot, Christophe Verny, et al.
Pageof 10