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Patrick F Chinnery

Neurology

Showing results (1-10 of 10) with videos related to

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Neurology|August 9, 2006
Progressive depletion of mtDNA in mitochondrial myopathySteve E Durham, Denise T Brown, Douglass M Turnbull, et al.
Neurology|September 6, 2015
Prevalence of neurogenetic disorders in the North of EnglandDavid Bargiela, Patrick Yu-Wai-Man, Michael Keogh, et al.
Neurology|November 8, 2013
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutationsGerald Pfeffer, Ailbhe Burke, Patrick Yu-Wai-Man, et al.
Neurology|August 12, 2016
Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort studyHannah E Steele, Elizabeth Harris, Rita Barresi, et al.
Neurology|April 22, 2021
[<sup>11</sup>C]PK11195-PET Brain Imaging of the Mitochondrial Translocator Protein in Mitochondrial DiseaseJelle van den Ameele, Young T Hong, Roido Manavaki, et al.
Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.
Neurology|May 4, 2018
Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo <i>PTEN</i> mutationBoglarka Bansagi, Vietxuan Phan, Mark R Baker, et al.
Neurology|March 3, 2017
Genetic heterogeneity of motor neuropathiesBoglarka Bansagi, Helen Griffin, Roger G Whittaker, et al.
Neurology|December 24, 2013
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD studyAlison J Yarnall, David P Breen, Gordon W Duncan, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Neurology|August 9, 2006
Progressive depletion of mtDNA in mitochondrial myopathySteve E Durham, Denise T Brown, Douglass M Turnbull, et al.
Neurology|September 6, 2015
Prevalence of neurogenetic disorders in the North of EnglandDavid Bargiela, Patrick Yu-Wai-Man, Michael Keogh, et al.
Neurology|November 8, 2013
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutationsGerald Pfeffer, Ailbhe Burke, Patrick Yu-Wai-Man, et al.
Neurology|August 12, 2016
Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort studyHannah E Steele, Elizabeth Harris, Rita Barresi, et al.
Neurology|April 22, 2021
[<sup>11</sup>C]PK11195-PET Brain Imaging of the Mitochondrial Translocator Protein in Mitochondrial DiseaseJelle van den Ameele, Young T Hong, Roido Manavaki, et al.
Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.
Neurology|May 4, 2018
Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo <i>PTEN</i> mutationBoglarka Bansagi, Vietxuan Phan, Mark R Baker, et al.
Neurology|March 3, 2017
Genetic heterogeneity of motor neuropathiesBoglarka Bansagi, Helen Griffin, Roger G Whittaker, et al.
Neurology|December 24, 2013
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD studyAlison J Yarnall, David P Breen, Gordon W Duncan, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
Pageof 1