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Simon Mead

Showing results (31-40 of 231) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|November 17, 2017
Imaging and CSF analyses effectively distinguish CJD from its mimicsPeter Rudge, Harpreet Hyare, Alison Green, et al.
JAMA Neurology|December 11, 2013
Creutzfeld-Jakob disease--replyHeather Angus-Leppan, Peter Rudge, Simon Mead, et al.
The Lancet. Neurology|January 24, 2026
Genetic causes and modifiers of prion diseasesSimon Mead, Peter Hermann, Tze How Mok, et al.
BMC Medical Genetics|September 17, 2009
HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10qSarah E Lloyd, Martin Rossor, Nick Fox, et al.
JAMA Neurology|May 24, 2013
Autoantibodies in sporadic Creutzfeldt-Jakob diseaseHeather Angus-Leppan, Peter Rudge, Simon Mead, et al.
International Psychogeriatrics|October 25, 2018
The most problematic symptoms of prion disease - an analysis of carer experiencesLiz Ford, Peter Rudge, Kathy Robinson, et al.
European Journal of Neurology|March 2, 2026
Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'Akin Nihat, Tze How Mok, Eric Vallabh Minikel, et al.
European Journal of Human Genetics : EJHG|June 26, 2022
Estimation of the number of inherited prion disease mutation carriers in the UKRosie Corbie, Tracy Campbell, Lee Darwent, et al.
Brain : a Journal of Neurology|May 21, 2024
Academic neurology in the UK: a plea to turn away from the precipiceHelen Devine, Edwin Jabbari, James Scott, et al.
Biological Psychiatry|May 13, 2018
Reply to: Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion ProteinSilvia A Purro, Simon Mead, Azadeh Khalili-Shirazi, et al.
Pageof 24

Showing results (31-40 of 231) with videos related to

Sort By:
Pageof 24
Journal of Neurology, Neurosurgery, and Psychiatry|November 17, 2017
Imaging and CSF analyses effectively distinguish CJD from its mimicsPeter Rudge, Harpreet Hyare, Alison Green, et al.
JAMA Neurology|December 11, 2013
Creutzfeld-Jakob disease--replyHeather Angus-Leppan, Peter Rudge, Simon Mead, et al.
The Lancet. Neurology|January 24, 2026
Genetic causes and modifiers of prion diseasesSimon Mead, Peter Hermann, Tze How Mok, et al.
BMC Medical Genetics|September 17, 2009
HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10qSarah E Lloyd, Martin Rossor, Nick Fox, et al.
JAMA Neurology|May 24, 2013
Autoantibodies in sporadic Creutzfeldt-Jakob diseaseHeather Angus-Leppan, Peter Rudge, Simon Mead, et al.
International Psychogeriatrics|October 25, 2018
The most problematic symptoms of prion disease - an analysis of carer experiencesLiz Ford, Peter Rudge, Kathy Robinson, et al.
European Journal of Neurology|March 2, 2026
Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'Akin Nihat, Tze How Mok, Eric Vallabh Minikel, et al.
European Journal of Human Genetics : EJHG|June 26, 2022
Estimation of the number of inherited prion disease mutation carriers in the UKRosie Corbie, Tracy Campbell, Lee Darwent, et al.
Brain : a Journal of Neurology|May 21, 2024
Academic neurology in the UK: a plea to turn away from the precipiceHelen Devine, Edwin Jabbari, James Scott, et al.
Biological Psychiatry|May 13, 2018
Reply to: Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion ProteinSilvia A Purro, Simon Mead, Azadeh Khalili-Shirazi, et al.
Pageof 24