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

Philip G Griffiths

Showing results (31-40 of 35) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 35 results.
Ophthalmology|April 27, 2010
The prevalence and natural history of dominant optic atrophy due to OPA1 mutationsPatrick Yu-Wai-Man, Philip G Griffiths, Ailbhe Burke, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEOLaura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
Brain : a Journal of Neurology|December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenanceGavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
Plos One|October 3, 2013
Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegiaCynthia Yu-Wai-Man, Fiona E Smith, Michael J Firbank, et al.
Brain : a Journal of Neurology|July 27, 2011
A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathyThomas Klopstock, Patrick Yu-Wai-Man, Konstantinos Dimitriadis, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Ophthalmology|April 27, 2010
The prevalence and natural history of dominant optic atrophy due to OPA1 mutationsPatrick Yu-Wai-Man, Philip G Griffiths, Ailbhe Burke, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEOLaura C Greaves, Patrick Yu-Wai-Man, Emma L Blakely, et al.
Brain : a Journal of Neurology|December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenanceGavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
Plos One|October 3, 2013
Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegiaCynthia Yu-Wai-Man, Fiona E Smith, Michael J Firbank, et al.
Brain : a Journal of Neurology|July 27, 2011
A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathyThomas Klopstock, Patrick Yu-Wai-Man, Konstantinos Dimitriadis, et al.
Pageof 4