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

Kevin Talbot

Showing results (221-230 of 255) with videos related to

Pageof 26
Sort By:
Brain : a Journal of Neurology|March 24, 2017
C9orf72 and RAB7L1 regulate vesicle trafficking in amyotrophic lateral sclerosis and frontotemporal dementiaYoshitsugu Aoki, Raquel Manzano, Yi Lee, et al.
Genome Research|December 23, 2016
Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network ResourceMichael J Keogh, Wei Wei, Ian Wilson, et al.
Acta Neuropathologica Communications|February 4, 2017
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brainsWei Wei, Michael J Keogh, Ian Wilson, et al.
Acta Neuropathologica Communications|February 24, 2017
Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brainsWei Wei, Michael J Keogh, Ian Wilson, et al.
The Lancet. Neurology|February 19, 2013
Controversies and priorities in amyotrophic lateral sclerosisMartin R Turner, Orla Hardiman, Michael Benatar, et al.
Progress in Neurobiology|December 5, 2025
Divergence of cortical neurophysiology across different neurodegenerative disorders compared to healthy ageingMichael Trubshaw, Oliver Kohl, Chetan Gohil, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Disease Models & Mechanisms|May 28, 2009
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathyFrancesca Achilli, Virginie Bros-Facer, Hazel P Williams, et al.
Brain Communications|February 28, 2022
Multicentre appraisal of amyotrophic lateral sclerosis biofluid biomarkers shows primacy of blood neurofilament light chainAlexander G Thompson, Elizabeth Gray, Nick Verber, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Pageof 26

Showing results (221-230 of 255) with videos related to

Sort By:
Pageof 26
Brain : a Journal of Neurology|March 24, 2017
C9orf72 and RAB7L1 regulate vesicle trafficking in amyotrophic lateral sclerosis and frontotemporal dementiaYoshitsugu Aoki, Raquel Manzano, Yi Lee, et al.
Genome Research|December 23, 2016
Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network ResourceMichael J Keogh, Wei Wei, Ian Wilson, et al.
Acta Neuropathologica Communications|February 4, 2017
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brainsWei Wei, Michael J Keogh, Ian Wilson, et al.
Acta Neuropathologica Communications|February 24, 2017
Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brainsWei Wei, Michael J Keogh, Ian Wilson, et al.
The Lancet. Neurology|February 19, 2013
Controversies and priorities in amyotrophic lateral sclerosisMartin R Turner, Orla Hardiman, Michael Benatar, et al.
Progress in Neurobiology|December 5, 2025
Divergence of cortical neurophysiology across different neurodegenerative disorders compared to healthy ageingMichael Trubshaw, Oliver Kohl, Chetan Gohil, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Disease Models & Mechanisms|May 28, 2009
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathyFrancesca Achilli, Virginie Bros-Facer, Hazel P Williams, et al.
Brain Communications|February 28, 2022
Multicentre appraisal of amyotrophic lateral sclerosis biofluid biomarkers shows primacy of blood neurofilament light chainAlexander G Thompson, Elizabeth Gray, Nick Verber, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Pageof 26