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 (71-80 of 370) with videos related to

Pageof 37
Sort By:
Journal of Neuromuscular Diseases|November 19, 2016
Adult-onset Mendelian PEO Associated with Mitochondrial DiseaseEwen W Sommerville, Patrick F Chinnery, Gráinne S Gorman, et al.
Biochimica Et Biophysica Acta|December 4, 2004
The epidemiology of mitochondrial disorders--past, present and futureAndrew M Schaefer, Robert W Taylor, Douglass M Turnbull, et al.
Neurology|August 9, 2006
Progressive depletion of mtDNA in mitochondrial myopathySteve E Durham, Denise T Brown, Douglass M Turnbull, et al.
The Cochrane Database of Systematic Reviews|April 20, 2012
Treatment for mitochondrial disordersGerald Pfeffer, Kari Majamaa, Douglass M Turnbull, et al.
American Journal of Human Genetics|June 15, 2007
Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->GSteve E Durham, David C Samuels, Lynsey M Cree, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 11, 2004
The role of apolipoprotein E gene polymorphisms in primary open-angle glaucomaThomas Ressiniotis, Philip G Griffiths, Michael Birch, et al.
Nucleic Acids Research|October 8, 2003
A compositional segmentation of the human mitochondrial genome is related to heterogeneities in the guanine mutation rateDavid C Samuels, Richard J Boys, Daniel A Henderson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 29, 2007
An investigation of mitochondrial haplogroups in autismLindsey Kent, Louise Gallagher, Hannah R Elliott, et al.
Annals of Neurology|May 4, 2004
Molecular epidemiology of spinocerebellar ataxia type 6Kate Craig, Sharon M Keers, Kate Archibald, et al.
Neurogenetics|January 27, 2012
Neuroferritinopathy: a new inborn error of iron metabolismMichael J Keogh, Patricia Jonas, Alan Coulthard, et al.
Pageof 37

Showing results (71-80 of 370) with videos related to

Sort By:
Pageof 37
Journal of Neuromuscular Diseases|November 19, 2016
Adult-onset Mendelian PEO Associated with Mitochondrial DiseaseEwen W Sommerville, Patrick F Chinnery, Gráinne S Gorman, et al.
Biochimica Et Biophysica Acta|December 4, 2004
The epidemiology of mitochondrial disorders--past, present and futureAndrew M Schaefer, Robert W Taylor, Douglass M Turnbull, et al.
Neurology|August 9, 2006
Progressive depletion of mtDNA in mitochondrial myopathySteve E Durham, Denise T Brown, Douglass M Turnbull, et al.
The Cochrane Database of Systematic Reviews|April 20, 2012
Treatment for mitochondrial disordersGerald Pfeffer, Kari Majamaa, Douglass M Turnbull, et al.
American Journal of Human Genetics|June 15, 2007
Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->GSteve E Durham, David C Samuels, Lynsey M Cree, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 11, 2004
The role of apolipoprotein E gene polymorphisms in primary open-angle glaucomaThomas Ressiniotis, Philip G Griffiths, Michael Birch, et al.
Nucleic Acids Research|October 8, 2003
A compositional segmentation of the human mitochondrial genome is related to heterogeneities in the guanine mutation rateDavid C Samuels, Richard J Boys, Daniel A Henderson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 29, 2007
An investigation of mitochondrial haplogroups in autismLindsey Kent, Louise Gallagher, Hannah R Elliott, et al.
Annals of Neurology|May 4, 2004
Molecular epidemiology of spinocerebellar ataxia type 6Kate Craig, Sharon M Keers, Kate Archibald, et al.
Neurogenetics|January 27, 2012
Neuroferritinopathy: a new inborn error of iron metabolismMichael J Keogh, Patricia Jonas, Alan Coulthard, et al.
Pageof 37