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Simon Mead

Showing results (61-70 of 231) with videos related to

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Journal of Neurology|April 1, 2022
Assessing initial MRI reports for suspected CJD patientsAaron Jesuthasan, Danielle Sequeira, Harpreet Hyare, et al.
The Lancet Regional Health. Europe|December 30, 2025
Estimating future variant Creutzfeldt-Jakob disease cases in the UK: a cohort-based probabilistic modelBarnaby Roberts, James Riley, Thomas J Evans, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Neuropathology and Applied Neurobiology|November 30, 2013
A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementiaTammaryn Lashley, Jonathan D Rohrer, Colin Mahoney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 12, 2011
11C-PiB PET does not detect PrP-amyloid in prion disease patients including variant Creutzfeldt-Jakob diseaseHarpreet Hyare, Anil Ramlackhansingh, Giorgio Gelosa, et al.
JAMA Neurology|October 5, 2016
Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient UrineConnie Luk, Samantha Jones, Claire Thomas, et al.
Acta Neuropathologica|February 17, 2018
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgeryZane Jaunmuktane, Annelies Quaegebeur, Ricardo Taipa, et al.
Archives of Neurology|December 12, 2007
Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British womanSimon Mead, Susan Joiner, Melanie Desbruslais, et al.
Brain Communications|August 17, 2022
Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob diseaseAkın Nihat, Janice M Ranson, Dominique Harris, et al.
BMC Medical Genetics|April 9, 2016
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international studyRubika Balendra, James Uphill, Claire Collinson, et al.
Pageof 24

Showing results (61-70 of 231) with videos related to

Sort By:
Pageof 24
Journal of Neurology|April 1, 2022
Assessing initial MRI reports for suspected CJD patientsAaron Jesuthasan, Danielle Sequeira, Harpreet Hyare, et al.
The Lancet Regional Health. Europe|December 30, 2025
Estimating future variant Creutzfeldt-Jakob disease cases in the UK: a cohort-based probabilistic modelBarnaby Roberts, James Riley, Thomas J Evans, et al.
Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.
Neuropathology and Applied Neurobiology|November 30, 2013
A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementiaTammaryn Lashley, Jonathan D Rohrer, Colin Mahoney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 12, 2011
11C-PiB PET does not detect PrP-amyloid in prion disease patients including variant Creutzfeldt-Jakob diseaseHarpreet Hyare, Anil Ramlackhansingh, Giorgio Gelosa, et al.
JAMA Neurology|October 5, 2016
Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient UrineConnie Luk, Samantha Jones, Claire Thomas, et al.
Acta Neuropathologica|February 17, 2018
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgeryZane Jaunmuktane, Annelies Quaegebeur, Ricardo Taipa, et al.
Archives of Neurology|December 12, 2007
Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British womanSimon Mead, Susan Joiner, Melanie Desbruslais, et al.
Brain Communications|August 17, 2022
Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob diseaseAkın Nihat, Janice M Ranson, Dominique Harris, et al.
BMC Medical Genetics|April 9, 2016
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international studyRubika Balendra, James Uphill, Claire Collinson, et al.
Pageof 24