Prion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?

por Ritchie, Diane L., Barria, Marcelo A.
Publicado 2021

Variant CJD: Reflections a Quarter of a Century on

por Ritchie, Diane L., Peden, Alexander H., Barria, Marcelo A.
Publicado 2021

Study protocol for enhanced CJD surveillance in the 65+ years population group in Scotland: an observational neuropathological screening study of banked brain tissue donations for...

por Peden, Alexander Howard, Kanguru, Lovney, Ritchie, Diane L, Smith, Colin, Molesworth, Anna M
Publicado 2019

Novel Morphological Glial Alterations in the Spectrum of Prion Disease Types: A Focus on Common Findings

por Garcés, Moisés, Guijarro, Isabel M., Ritchie, Diane L., Badiola, Juan J., Monzón, Marta
Publicado 2021

Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathies

por De Sousa, Paul A., Ritchie, Diane, Green, Alison, Chandran, Siddharthan, Knight, Richard, Head, Mark W.
Publicado 2018

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob disease

por Bishop, Matthew T., Diack, Abigail B., Ritchie, Diane L., Ironside, James W., Will, Robert G., Manson, Jean C.
Publicado 2013

Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes

por Ward, Anne, Hollister, Jason R., McNally, Kristin, Ritchie, Diane L., Zanusso, Gianluigi, Priola, Suzette A.
Publicado 2020

A Naturally Occurring Bovine Tauopathy Is Geographically Widespread in the UK

por Jeffrey, Martin, Piccardo, Pedro, Ritchie, Diane L., Ironside, James W., Green, Alison J. E., McGovern, Gillian
Publicado 2015

No Major Change in vCJD Agent Strain after Secondary Transmission via Blood Transfusion

por Bishop, Matthew T., Ritchie, Diane L., Will, Robert G., Ironside, James W., Head, Mark W., Thomson, Val, Bruce, Moira, Manson, Jean C.
Publicado 2008

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

por Moore, Roger A., Head, Mark W., Ironside, James W., Ritchie, Diane L., Zanusso, Gianluigi, Pyo Choi, Young, Priola, Suzette A.
Publicado 2016

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

por Moore, Roger A., Head, Mark W., Ironside, James W., Ritchie, Diane L., Zanusso, Gianluigi, Choi, Young Pyo, Priola, Suzette A.
Publicado 2016

The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt...

por Peden, Alexander H, Sarode, Deep P, Mulholland, Carl R, Barria, Marcelo A, Ritchie, Diane L, Ironside, James W, Head, Mark W
Publicado 2014

UK Iatrogenic Creutzfeldt–Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches

por Ritchie, Diane L., Barria, Marcelo A., Peden, Alexander H., Yull, Helen M., Kirkpatrick, James, Adlard, Peter, Ironside, James W., Head, Mark W.
Publicado 2016

Similarities of Variant Creutzfeldt-Jakob Disease Strain in Mother and Son in Spain to UK Reference Case

por Diack, Abigail B., Boyle, Aileen, Ritchie, Diane, Plinston, Chris, Kisielewski, Dorothy, de Pedro-Cuesta, Jesús, Rábano, Alberto, Will, Robert G., Manson, Jean C.
Publicado 2017

Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrP(Sc) from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein M...

por Suleiman, Suzanne, McGuire, Lynne I., Chong, Angela, Ritchie, Diane L., Boyle, Aileen, McManus, Lee, Brydon, Fraser, Smith, Colin, Knight, Richard, Green, Alison, Diack, Abigail B., Barria, Marcelo A.
Publicado 2023

Variably Protease-Sensitive Prionopathy, a Unique Prion Variant with Inefficient Transmission Properties

por Diack, Abigail B., Ritchie, Diane L., Peden, Alexander H., Brown, Deborah, Boyle, Aileen, Morabito, Laura, Maclennan, David, Burgoyne, Paul, Jansen, Casper, Knight, Richard S., Piccardo, Pedro, Ironside, James W., Manson, Jean C.
Publicado 2014

Constant Transmission Properties of Variant Creutzfeldt-Jakob Disease in 5 Countries

por Diack, Abigail B., Ritchie, Diane, Bishop, Matthew, Pinion, Victoria, Brandel, Jean-Philippe, Haik, Stephane, Tagliavini, Fabrizio, Van Duijn, Cornelia, Belay, Ermias D., Gambetti, Pierluigi, Schonberger, Lawrence B., Piccardo, Pedro, Will, Robert G., Manson, Jean C.
Publicado 2012

Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK

por Ritchie, Diane L., Adlard, Peter, Peden, Alexander H., Lowrie, Suzanne, Le Grice, Margaret, Burns, Kimberley, Jackson, Rosemary J., Yull, Helen, Keogh, Michael J., Wei, Wei, Chinnery, Patrick F., Head, Mark W., Ironside, James W.
Publicado 2017

Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey

por Clewley, Jonathan P, Kelly, Carole M, Andrews, Nick, Vogliqi, Kelly, Mallinson, Gary, Kaisar, Maria, Hilton, David A, Ironside, James W, Edwards, Philip, McCardle, Linda M, Ritchie, Diane L, Dabaghian, Reza, Ambrose, Helen E, Gill, O Noel
Publicado 2009

Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification

por Baiardi, Simone, Rossi, Marcello, Mammana, Angela, Appleby, Brian S., Barria, Marcelo A., Calì, Ignazio, Gambetti, Pierluigi, Gelpi, Ellen, Giese, Armin, Ghetti, Bernardino, Herms, Jochen, Ladogana, Anna, Mikol, Jacqueline, Pal, Suvankar, Ritchie, Diane L., Ruf, Viktoria, Windl, Otto, Capellari, Sabina, Parchi, Piero
Publicado 2021