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

Patrick F Chinnery

Showing results (51-60 of 473) with videos related to

Pageof 48
Sort By:
Brain : a Journal of Neurology|August 19, 2015
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutationPatrick Yu-Wai-Man, Patrick F Chinnery
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|November 21, 2008
How can we treat mitochondrial encephalomyopathies? Approaches to therapyRita Horvath, Grainne Gorman, Patrick F Chinnery
Brain : a Journal of Neurology|July 12, 2014
Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Patrick Yu-Wai-Man, Patrick F Chinnery
Handbook of Clinical Neurology|February 22, 2023
PrefaceRita Horvath, Michio Hirano, Patrick F Chinnery
Brain : a Journal of Neurology|January 25, 2012
Dysfunctional mitochondrial maintenance: what breaks the circle of life?Patrick Yu-Wai-Man, Patrick F Chinnery
Neurology|May 18, 2011
AMACR mutations cause late-onset autosomal recessive cerebellar ataxiaDavid Dick, Rita Horvath, Patrick F Chinnery
Brain : a Journal of Neurology|May 8, 2013
Reply: Sensorineural hearing loss in OPA1-linked disordersPatrick Yu-Wai-Man, Patrick F Chinnery
Ophthalmology|August 7, 2013
Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimatesPatrick Yu-Wai-Man, Patrick F Chinnery
Annals of Neurology|January 23, 2015
Increased yield of exome sequencing by off-target mitochondrial DNA analysisHelen Griffin, Angela Pyle, Patrick F Chinnery
Cell Metabolism|January 3, 2024
Show MERCI on mobile mitochondriaJelle van den Ameele, Patrick F Chinnery
Pageof 48

Showing results (51-60 of 473) with videos related to

Sort By:
Pageof 48
Brain : a Journal of Neurology|August 19, 2015
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutationPatrick Yu-Wai-Man, Patrick F Chinnery
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|November 21, 2008
How can we treat mitochondrial encephalomyopathies? Approaches to therapyRita Horvath, Grainne Gorman, Patrick F Chinnery
Brain : a Journal of Neurology|July 12, 2014
Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Patrick Yu-Wai-Man, Patrick F Chinnery
Handbook of Clinical Neurology|February 22, 2023
PrefaceRita Horvath, Michio Hirano, Patrick F Chinnery
Brain : a Journal of Neurology|January 25, 2012
Dysfunctional mitochondrial maintenance: what breaks the circle of life?Patrick Yu-Wai-Man, Patrick F Chinnery
Neurology|May 18, 2011
AMACR mutations cause late-onset autosomal recessive cerebellar ataxiaDavid Dick, Rita Horvath, Patrick F Chinnery
Brain : a Journal of Neurology|May 8, 2013
Reply: Sensorineural hearing loss in OPA1-linked disordersPatrick Yu-Wai-Man, Patrick F Chinnery
Ophthalmology|August 7, 2013
Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimatesPatrick Yu-Wai-Man, Patrick F Chinnery
Annals of Neurology|January 23, 2015
Increased yield of exome sequencing by off-target mitochondrial DNA analysisHelen Griffin, Angela Pyle, Patrick F Chinnery
Cell Metabolism|January 3, 2024
Show MERCI on mobile mitochondriaJelle van den Ameele, Patrick F Chinnery
Pageof 48