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 (81-90 of 92) with videos related to

Pageof 10
Sort By:
Plos One|September 23, 2016
COMT Val158Met Polymorphism Modulates Huntington's Disease ProgressionRuth de Diego-Balaguer, Catherine Schramm, Isabelle Rebeix, et al.
Neurobiology of Disease|July 14, 2009
A genetic variation in the ADORA2A gene modifies age at onset in Huntington's diseaseClaire-Marie Dhaenens, Sylvie Burnouf, Clémence Simonin, et al.
Investigative Ophthalmology & Visual Science|February 5, 2017
Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1delTTAG/+ MiceJuan Manuel Chao de la Barca, Gilles Simard, Emmanuelle Sarzi, et al.
Brain : a Journal of Neurology|September 17, 2016
The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stressJuan Manuel Chao de la Barca, Gilles Simard, Patrizia Amati-Bonneau, et al.
Neurobiology of Disease|June 5, 2013
Association between caffeine intake and age at onset in Huntington's diseaseClémence Simonin, Cécile Duru, Julia Salleron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2021
Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disordersCeline Bris, David Goudenège, Valerie Desquiret-Dumas, et al.
Brain : a Journal of Neurology|September 26, 2013
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, Camille Charbonnier, et al.
Brain : a Journal of Neurology|December 26, 2007
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesPatrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, et al.
Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
Annals of Neurology|August 21, 2015
New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-SaguenayJulie Pilliod, Sébastien Moutton, Julie Lavie, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Plos One|September 23, 2016
COMT Val158Met Polymorphism Modulates Huntington's Disease ProgressionRuth de Diego-Balaguer, Catherine Schramm, Isabelle Rebeix, et al.
Neurobiology of Disease|July 14, 2009
A genetic variation in the ADORA2A gene modifies age at onset in Huntington's diseaseClaire-Marie Dhaenens, Sylvie Burnouf, Clémence Simonin, et al.
Investigative Ophthalmology & Visual Science|February 5, 2017
Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1delTTAG/+ MiceJuan Manuel Chao de la Barca, Gilles Simard, Emmanuelle Sarzi, et al.
Brain : a Journal of Neurology|September 17, 2016
The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stressJuan Manuel Chao de la Barca, Gilles Simard, Patrizia Amati-Bonneau, et al.
Neurobiology of Disease|June 5, 2013
Association between caffeine intake and age at onset in Huntington's diseaseClémence Simonin, Cécile Duru, Julia Salleron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2021
Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disordersCeline Bris, David Goudenège, Valerie Desquiret-Dumas, et al.
Brain : a Journal of Neurology|September 26, 2013
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, Camille Charbonnier, et al.
Brain : a Journal of Neurology|December 26, 2007
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesPatrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, et al.
Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
Annals of Neurology|August 21, 2015
New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-SaguenayJulie Pilliod, Sébastien Moutton, Julie Lavie, et al.
Pageof 10