CJD mimics and chameleons

por Mead, Simon, Rudge, Peter
Publicado 2017

Detection of Creutzfeldt-Jakob disease prions in skin: implications for healthcare

por Nihat, Akin, Mead, Simon
Publicado 2018

The Future of Seed Amplification Assays and Clinical Trials

por Coysh, Thomas, Mead, Simon
Publicado 2022

Gene expression and epigenetic markers of prion diseases

por Viré, Emmanuelle A., Mead, Simon
Publicado 2022

Genetics of prion diseases

por Lloyd, Sarah E, Mead, Simon, Collinge, John
Publicado 2013

Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease

por Rossi, Meghan, Mead, Simon, Collinge, John, Rudge, Peter, Vincent, Angela
Publicado 2015

Imaging and CSF analyses effectively distinguish CJD from its mimics

por Rudge, Peter, Hyare, Harpreet, Green, Alison, Collinge, John, Mead, Simon
Publicado 2018

HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q

por Lloyd, Sarah E, Rossor, Martin, Fox, Nick, Mead, Simon, Collinge, John
Publicado 2009

Estimation of the number of inherited prion disease mutation carriers in the UK

por Corbie, Rosie, Campbell, Tracy, Darwent, Lee, Rudge, Peter, Collinge, John, Mead, Simon
Publicado 2022

Tau, prions and Aβ: the triad of neurodegeneration

por Reiniger, Lilla, Lukic, Ana, Linehan, Jacqueline, Rudge, Peter, Collinge, John, Mead, Simon, Brandner, Sebastian
Publicado 2010

The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature

por Caine, Diana, Nihat, Akin, Crabb, Philippa, Rudge, Peter, Cipolotti, Lisa, Collinge, John, Mead, Simon
Publicado 2018

Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease

por Hassan, Ahamad, Campbell, Tracy, Darwent, Lee, Odd, Hans, Green, Alison, Collinge, John, Mead, Simon
Publicado 2021

Prion protein gene mutation detection using long-read Nanopore sequencing

por Kroll, François, Dimitriadis, Athanasios, Campbell, Tracy, Darwent, Lee, Collinge, John, Mead, Simon, Vire, Emmanuelle
Publicado 2022

Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study

por Sequeira, Danielle, Nihat, Akin, Mok, Tzehow, Coysh, Thomas, Rudge, Peter, Collinge, John, Mead, Simon
Publicado 2022

Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutation

por Themistocleous, Andreas C., Kennett, Robin, Husain, Masud, Palace, Jacqueline, Mead, Simon, Bennett, David L. H.
Publicado 2014

MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease

por Carswell, Christopher, Thompson, Andrew, Lukic, Ana, Stevens, John, Rudge, Peter, Mead, Simon, Collinge, John, Hyare, Harpreet
Publicado 2012

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

por Rudge, Peter, Jaunmuktane, Zane, Hyare, Harpreet, Ellis, Matthew, Koltzenburg, Martin, Collinge, John, Brandner, Sebastian, Mead, Simon
Publicado 2019

Familial Creutzfeldt-Jakob Disease in an Indian Kindred

por Katrak, Sarosh M., Pauranik, Apoorva, Desai, Shrinivas B., Mead, Simon, Beck, Jon, Brandner, Sebastian, Collinge, John
Publicado 2019

Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases

por Mok, Tze How, Nihat, Akin, Luk, Connie, Sequeira, Danielle, Batchelor, Mark, Mead, Simon, Collinge, John, Jackson, Graham S.
Publicado 2021

Neurofilament light chain and tau concentrations are markedly increased in the serum of patients with sporadic Creutzfeldt-Jakob disease, and tau correlates with rate of disease pr...

por Thompson, Andrew Geoffrey Bourne, Luk, Connie, Heslegrave, Amanda J, Zetterberg, Henrik, Mead, Simon H, Collinge, John, Jackson, Graham S
Publicado 2018