Works by Ritchie, Diane L.

Results: 23

Variant CJD: Reflections a Quarter of a Century on.

Published in:

Pathogens, 2021, v. 10, n. 11, p. 1413, doi. 10.3390/pathogens10111413

By:

Ritchie, Diane L.;
Peden, Alexander H.;
Barria, Marcelo A.

Publication type:

Article

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

Published in:

Pathogens, 2021, v. 10, n. 5, p. 596, doi. 10.3390/pathogens10050596

By:

Garcés, Moisés;
Guijarro, Isabel M.;
Ritchie, Diane L.;
Badiola, Juan J.;
Monzón, Marta;
Zou, Wen-Quan

Publication type:

Article

P.145: Assessing the risk of transmission of prion infectivity by blood transfusion in a non-human primate model: The Baxter study.

Published in:

Prion, 2014, v. 8, p. 92

By:

Ritchie, Diane L.;
Brown, Paul;
Gibson, Susan;
Kreil, Thomas R.;
Abee, Christian;
Ironside, James W.

Publication type:

Article

O.13: Variable protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties.

Published in:

Prion, 2014, v. 8, p. 17

By:

Diack, Abigail B.;
Ritchie, Diane L.;
Peden, Alexander H.;
Brown, Deborah;
Boyle, Aileen;
Morabito, Laura;
Maclennan, David;
Burgoyne, Paul;
Piccardo, Pedro;
Ironside, James W.;
Manson, Jean C.

Publication type:

Article

Enhanced Creutzfeldt‐Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease.

Published in:

Brain Pathology, 2024, v. 34, n. 2, p. 1, doi. 10.1111/bpa.13214

By:

Peden, Alexander H.;
Libori, Adriana;
Ritchie, Diane L.;
Yull, Helen;
Smith, Colin;
Kanguru, Lovney;
Molesworth, Anna;
Knight, Richard;
Barria, Marcelo A.

Publication type:

Article

Risks of transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

Published in:

Folia Neuropathologica, 2005, v. 43, n. 4, p. 271

By:

Peden, Alexander H.;
Ritchie, Diane L.;
Ironside, James W.

Publication type:

Article

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

Published in:

Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-00958-x

By:

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

Publication type:

Article

Characterization of variably protease-sensitive prionopathy by capillary electrophoresis.

Published in:

Scientific Reports, 2024, v. 12, n. 1, p. 1, doi. 10.1038/s41598-024-79217-1

By:

Myskiw, Jennifer;
Bailey-Elkin, Ben A.;
Avery, Kristen;
Barria, Marcelo A.;
Ritchie, Diane L.;
Cohen, Mark L.;
Appleby, Brian S.;
Booth, Stephanie A

Publication type:

Article

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

Published in:

Biomolecules (2218-273X), 2021, v. 11, n. 2, p. 207, doi. 10.3390/biom11020207

By:

Ritchie, Diane L.;
Barria, Marcelo A.

Publication type:

Article

Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.

Published in:

2018

By:

Abu‐Rumeileh, Samir;
Redaelli, Veronica;
Baiardi, Simone;
Mackenzie, Graeme;
Windl, Otto;
Ritchie, Diane L.;
Didato, Giuseppe;
Hernandez‐Vara, Jorge;
Rossi, Marcello;
Capellari, Sabina;
Imperiale, Daniele;
Rizzone, Mario Giorgio;
Belotti, Alessia;
Sorbi, Sandro;
Rozemuller, Annemieke J. M.;
Cortelli, Pietro;
Gelpi, Ellen;
Will, Robert G.;
Zerr, Inga;
Giaccone, Giorgio

Publication type:

journal article

Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties.

Published in:

2014

By:

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

Publication type:

journal article

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

Published in:

2016

By:

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

Publication type:

Correction Notice

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

Published in:

PLoS Pathogens, 2016, v. 12, n. 2, p. 1, doi. 10.1371/journal.ppat.1005416

By:

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

Publication type:

Article

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

Published in:

Acta Neuropathologica, 2021, v. 142, n. 4, p. 707, doi. 10.1007/s00401-021-02350-y

By:

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

Publication type:

Article

Blood transmission studies of prion infectivity in the squirrel monkey (Saimiri sciureus): the Baxter study.

Published in:

2016

By:

Ritchie, Diane L.;
Gibson, Susan V.;
Abee, Christian R.;
Kreil, Thomas R.;
Ironside, James W.;
Brown, Paul

Publication type:

journal article

Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrP<sup>Sc</sup> from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein Misfolding Cyclic Amplification.

Published in:

Molecular Neurobiology, 2023, v. 60, n. 11, p. 6275, doi. 10.1007/s12035-023-03444-2

By:

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.

Publication type:

Article

Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients.

Published in:

Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01247-x

By:

Douet, Jean-Yves;
Huor, Alvina;
Cassard, Hervé;
Lugan, Séverine;
Aron, Naïma;
Mesic, Chloé;
Vilette, Didier;
Barrio, Tomás;
Streichenberger, Nathalie;
Perret-Liaudet, Armand;
Delisle, Marie-Bernadette;
Péran, Patrice;
Deslys, Jean-Philippe;
Comoy, Emmanuel;
Vilotte, Jean-Luc;
Goudarzi, Katayoun;
Béringue, Vincent;
Barria, Marcelo A.;
Ritchie, Diane L.;
Ironside, James W.

Publication type:

Article

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

Published in:

PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002878

By:

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

Publication type:

Article

A Naturally Occurring Bovine Tauopathy Is Geographically Widespread in the UK.

Published in:

PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0129499

By:

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

Publication type:

Article

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991-2008.

Published in:

2013

By:

Head, Mark W;
Yull, Helen M;
Ritchie, Diane L;
Langeveld, Jan P;
Fletcher, Nicholas A;
Knight, Richard S;
Ironside, James W

Publication type:

journal article

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

Published in:

2013

By:

Bishop, Matthew T;
Diack, Abigail B;
Ritchie, Diane L;
Ironside, James W;
Will, Robert G;
Manson, Jean C

Publication type:

journal article

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991–2008.

Published in:

Brain: A Journal of Neurology, 2013, v. 136, n. 4, p. 1102, doi. 10.1093/brain/aws366

By:

Head, Mark W.;
Yull, Helen M.;
Ritchie, Diane L.;
Langeveld, Jan P.;
Fletcher, Nicholas A.;
Knight, Richard S.;
Ironside, James W.

Publication type:

Article

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

Published in:

Brain: A Journal of Neurology, 2013, v. 136, n. 4, p. 1139, doi. 10.1093/brain/awt032

By:

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

Publication type:

Article