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James G Colebatch

Showing results (101-110 of 110) with videos related to

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Plos One|May 15, 2018
The provision of written information and its effect on levels of pain and anxiety during electrodiagnostic studies: A randomised controlled trialYan Ling Lai, Annemarie Van Heuven, Adeniyi Borire, et al.
Journal of Neural Engineering|October 29, 2025
Feasibility of decoding cerebellar movement-related potentials for brain-computer interface applicationsJohn S Russo, James G Colebatch, Chin-Hsuan Sophie Lin, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|January 10, 2025
Topical review: Ocular surface abnormalities in neurodegenerative disordersSophie E Waller, Joseph B Stockwell, Victor S C Fung, et al.
European Journal of Neurology|October 15, 2024
Video head impulse gain is impaired in myotonic dystrophy types 1 and 2Zeljka Calic, Stojan Peric, Milorad Vujnic, et al.
Muscle & Nerve|May 27, 2016
Utility of maximum perfusion intensity as an ultrasonographic marker of intraneural blood flowAdeniyi A Borire, Leo H Visser, Luca Padua, et al.
Movement Disorders Clinical Practice|October 27, 2018
Resolution of Othello Syndrome After Subthalamic Nucleus Deep Brain Stimulation in 3 Patients with Parkinson's DiseaseRobert J Adam, Robert McLeod, Ainhi D Ha, et al.
Movement Disorders Clinical Practice|April 6, 2019
Deep Brain Stimulation as Management of Generalized Dystonia in the 18p Deletion SyndromeStephen R Duma, Alessandro F Fois, Hugo Morales-Briceño, et al.
Neurology|November 3, 2017
Practice guideline: Cervical and ocular vestibular evoked myogenic potential testing: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of NeurologyTerry D Fife, James G Colebatch, Kevin A Kerber, et al.
Human Molecular Genetics|June 19, 2013
Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)Melody Caramins, James G Colebatch, Matthew N Bainbridge, et al.
Cerebellum (London, England)|August 6, 2018
High Degree of Genetic Heterogeneity for Hereditary Cerebellar Ataxias in AustraliaCe Kang, Christina Liang, Kate E Ahmad, et al.
Pageof 11

Showing results (101-110 of 110) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 110 results.
Plos One|May 15, 2018
The provision of written information and its effect on levels of pain and anxiety during electrodiagnostic studies: A randomised controlled trialYan Ling Lai, Annemarie Van Heuven, Adeniyi Borire, et al.
Journal of Neural Engineering|October 29, 2025
Feasibility of decoding cerebellar movement-related potentials for brain-computer interface applicationsJohn S Russo, James G Colebatch, Chin-Hsuan Sophie Lin, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|January 10, 2025
Topical review: Ocular surface abnormalities in neurodegenerative disordersSophie E Waller, Joseph B Stockwell, Victor S C Fung, et al.
European Journal of Neurology|October 15, 2024
Video head impulse gain is impaired in myotonic dystrophy types 1 and 2Zeljka Calic, Stojan Peric, Milorad Vujnic, et al.
Muscle & Nerve|May 27, 2016
Utility of maximum perfusion intensity as an ultrasonographic marker of intraneural blood flowAdeniyi A Borire, Leo H Visser, Luca Padua, et al.
Movement Disorders Clinical Practice|October 27, 2018
Resolution of Othello Syndrome After Subthalamic Nucleus Deep Brain Stimulation in 3 Patients with Parkinson's DiseaseRobert J Adam, Robert McLeod, Ainhi D Ha, et al.
Movement Disorders Clinical Practice|April 6, 2019
Deep Brain Stimulation as Management of Generalized Dystonia in the 18p Deletion SyndromeStephen R Duma, Alessandro F Fois, Hugo Morales-Briceño, et al.
Neurology|November 3, 2017
Practice guideline: Cervical and ocular vestibular evoked myogenic potential testing: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of NeurologyTerry D Fife, James G Colebatch, Kevin A Kerber, et al.
Human Molecular Genetics|June 19, 2013
Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)Melody Caramins, James G Colebatch, Matthew N Bainbridge, et al.
Cerebellum (London, England)|August 6, 2018
High Degree of Genetic Heterogeneity for Hereditary Cerebellar Ataxias in AustraliaCe Kang, Christina Liang, Kate E Ahmad, et al.
Pageof 11