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 (191-200 of 473) with videos related to

Pageof 48
Sort By:
BMJ Neurology Open|June 11, 2024
Evidence for sodium valproate toxicity in mitochondrial diseases: a systematic analysisThiloka E Ratnaike, Nour Elkhateeb, Angela Lochmüller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 17, 2021
Isolated homozygous R217X <i>OPTN</i> mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDPMatthew Nolan, Paola Barbagallo, Martin R Turner, et al.
Neurogenetics|November 4, 2006
Mitochondrial DNA haplogroups and amyotrophic lateral sclerosisPatrick F Chinnery, Catherine Mowbray, Hannah Elliot, et al.
Journal of Neurology|May 11, 2015
Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filteringDaniyal Daud, Helen Griffin, Konstantinos Douroudis, et al.
Interface Focus|December 27, 2021
How COVID-19 has changed medical research fundingPatrick F Chinnery, Jonathan J Pearce, Anna M Kinsey, et al.
Neurology. Clinical Practice|April 6, 2018
<i>PLP1</i> mutations and central demyelination: Evidence from electrophysiologic phenotyping in female manifesting carriersMichael J Keogh, Stephan R Jaiser, Hannah E Steele, et al.
Neurotrauma Reports|October 7, 2022
Cell-Free Mitochondrial DNA in Acute Brain InjurySaeed Kayhanian, Angelos Glynos, Richard Mair, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Neurology. Genetics|January 23, 2023
High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob DiseaseAlexander G Murley, Yu Nie, Zoe Golder, et al.
Pageof 48

Showing results (191-200 of 473) with videos related to

Sort By:
Pageof 48
BMJ Neurology Open|June 11, 2024
Evidence for sodium valproate toxicity in mitochondrial diseases: a systematic analysisThiloka E Ratnaike, Nour Elkhateeb, Angela Lochmüller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 17, 2021
Isolated homozygous R217X <i>OPTN</i> mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDPMatthew Nolan, Paola Barbagallo, Martin R Turner, et al.
Neurogenetics|November 4, 2006
Mitochondrial DNA haplogroups and amyotrophic lateral sclerosisPatrick F Chinnery, Catherine Mowbray, Hannah Elliot, et al.
Journal of Neurology|May 11, 2015
Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filteringDaniyal Daud, Helen Griffin, Konstantinos Douroudis, et al.
Interface Focus|December 27, 2021
How COVID-19 has changed medical research fundingPatrick F Chinnery, Jonathan J Pearce, Anna M Kinsey, et al.
Neurology. Clinical Practice|April 6, 2018
<i>PLP1</i> mutations and central demyelination: Evidence from electrophysiologic phenotyping in female manifesting carriersMichael J Keogh, Stephan R Jaiser, Hannah E Steele, et al.
Neurotrauma Reports|October 7, 2022
Cell-Free Mitochondrial DNA in Acute Brain InjurySaeed Kayhanian, Angelos Glynos, Richard Mair, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Neurology. Genetics|January 23, 2023
High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob DiseaseAlexander G Murley, Yu Nie, Zoe Golder, et al.
Pageof 48