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Simon Mead

Showing results (171-180 of 231) with videos related to

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Journal of Neurology|March 29, 2025
PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Neurobiology of Disease|November 23, 2023
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6Emma Jones, Elizabeth Hill, Jacqueline Linehan, et al.
Acta Neuropathologica|April 2, 2020
Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizooticO Noel Gill, Yvonne Spencer, Angela Richard-Loendt, et al.
Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
JAMA Neurology|February 24, 2016
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.
Neurology|September 2, 2016
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementiaJonathan D Rohrer, Ione O C Woollacott, Katrina M Dick, et al.
Acta Neuropathologica Communications|September 21, 2022
Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementiaSterre C M de Boer, Lauren Woolley, Merel O Mol, et al.
Pageof 24

Showing results (171-180 of 231) with videos related to

Sort By:
Pageof 24
Journal of Neurology|March 29, 2025
PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Neurobiology of Disease|November 23, 2023
Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6Emma Jones, Elizabeth Hill, Jacqueline Linehan, et al.
Acta Neuropathologica|April 2, 2020
Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizooticO Noel Gill, Yvonne Spencer, Angela Richard-Loendt, et al.
Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
JAMA Neurology|February 24, 2016
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.
Neurology|September 2, 2016
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementiaJonathan D Rohrer, Ione O C Woollacott, Katrina M Dick, et al.
Acta Neuropathologica Communications|September 21, 2022
Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementiaSterre C M de Boer, Lauren Woolley, Merel O Mol, et al.
Pageof 24