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Manuscripts | Pictures | Drawings | Photographs
Series 02: Allen & Unwin Further Production files, ca. 1976-1990
Date:1976-1990
Call Numbers:MLMSS 6686/Boxes 152-179
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Manuscripts | Pictures | Drawings | Photographs
Series 04: Allen & Unwin Further publisher files, ca. 1977-1990
Date:1977-1990
Call Numbers:MLMSS 6686/Boxes 224-253
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Pictures | Drawings | Photographs | Manuscripts
Series 08: Allen & Unwin cover art, ca. 1980-1990
Date:1980-1990
Call Numbers:MLMSS 6686/Boxes 272X-287X, Folder 288X
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Manuscripts | Drawings | Photographs
Series 01 Part 01: Allen & Unwin Production files. F Sequence, ca. 1980-1990
Date:1980-1990
Call Numbers:MLMSS 6686/Boxes 1-30
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ArticlesPeer ReviewedFull Text
Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification
Author / Creator: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
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2021-10, Vol.142 (4), p.707-728
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ArticlesPeer ReviewedFull Text
Prion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?
Author / Creator:Ritchie, Diane L ; Barria, Marcelo A
Publisher:Switzerland: MDPI AG
Journal title:Biomolecules (Basel, Switzerland), 2021-02, Vol.11 (2), p.207
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ArticlesPeer ReviewedFull Text
Characterization of variably protease-sensitive prionopathy by capillary electrophoresis
Author / Creator:Myskiw, Jennifer ; Bailey-Elkin, Ben A. ; Avery, Kristen ; Barria, Marcelo A. ; Ritchie, Diane L. ; Cohen, Mark L. ; Appleby, Brian S. ; Booth, Stephanie A
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2024-11, Vol.14 (1), p.27867-14, Article 27867
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ArticlesPeer ReviewedFull Text
Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient
Author / Creator:Peden, Alexander H ; Head, Mark W ; Diane, L Ritchie ; Jeanne, E Bell ; James, W Ironside
Publisher:London: Elsevier Ltd
Journal title:The Lancet (British edition), 2004-08, Vol.364 (9433), p.527-529
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ArticlesPeer ReviewedFull Text
Variant CJD: Reflections a Quarter of a Century on
Author / Creator:Ritchie, Diane L. ; Peden, Alexander H. ; Barria, Marcelo A.
Publisher:Basel: MDPI AG
Journal title:Pathogens (Basel), 2021-10, Vol.10 (11), p.1413
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Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes
Author / Creator:Ward, Anne ; Hollister, Jason R ; McNally, Kristin ; Ritchie, Diane L ; Zanusso, Gianluigi ; Priola, Suzette A
Publisher:London: BioMed Central Ltd
Journal title:Acta neuropathologica communications, 2020-06, Vol.8 (1), p.1-83, Article 83
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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 evidence of prion di...
Author / Creator:Peden, Alexander Howard ; Kanguru, Lovney ; Ritchie, Diane L ; Smith, Colin ; Molesworth, Anna M
Publisher:England: British Medical Journal Publishing Group
Journal title:BMJ open, 2019-10, Vol.9 (10), p.e033744-e033744
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ArticlesPeer ReviewedFull Text
The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients
Author / Creator:Moore, Roger A ; Head, Mark W ; Ironside, James W ; Ritchie, Diane L ; Zanusso, Gianluigi ; Choi, Young Pyo ; Pyo Choi, Young ; Priola, Suzette A
Publisher:United States: Public Library of Science
Journal title:PLoS pathogens, 2016-02, Vol.12 (2), p.e1005416-e1005416
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ArticlesPeer ReviewedFull Text
A Naturally Occurring Bovine Tauopathy Is Geographically Widespread in the UK
Author / Creator:Jeffrey, Martin ; Piccardo, Pedro ; Ritchie, Diane L ; Ironside, James W ; Green, Alison J E ; McGovern, Gillian
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-06, Vol.10 (6), p.e0129499
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ArticlesPeer ReviewedFull Text
Novel Morphological Glial Alterations in the Spectrum of Prion Disease Types: A Focus on Common Findings
Author / Creator:Garcés, Moisés ; Guijarro, Isabel M. ; Ritchie, Diane L. ; Badiola, Juan J. ; Monzón, Marta
Publisher:Basel: MDPI AG
Journal title:Pathogens (Basel), 2021-05, Vol.10 (5), p.596
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ArticlesPeer ReviewedFull Text
Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients
Author / Creator: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 ; Andréoletti, Olivier
Publisher:England: BioMed Central Ltd
Journal title:Acta neuropathologica communications, 2021-08, Vol.9 (1), p.145-145, Article 145
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ArticlesPeer ReviewedFull Text
Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients
Author / Creator:Moore, Roger A ; Head, Mark W ; Ironside, James W ; Ritchie, Diane L ; Zanusso, Gianluigi ; Choi, Young Pyo ; Priola, Suzette A
Publisher:United States: Public Library of Science
Journal title:PLoS pathogens, 2016-03, Vol.12 (3), p.e1005496
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ArticlesPeer ReviewedFull Text
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK
Author / Creator: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.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2017-08, Vol.134 (2), p.221-240
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ArticlesPeer ReviewedFull Text
Enhanced Creutzfeldt‐Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease
Author / Creator:Peden, Alexander H. ; Libori, Adriana ; Ritchie, Diane L. ; Yull, Helen ; Smith, Colin ; Kanguru, Lovney ; Molesworth, Anna ; Knight, Richard ; Barria, Marcelo A.
Publisher:Switzerland: John Wiley & Sons, Inc
Journal title:Brain pathology (Zurich, Switzerland), 2024-03, Vol.34 (2), p.e13214-n/a
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ArticlesPeer ReviewedFull Text
No major change in vCJD agent strain after secondary transmission via blood transfusion
Author / Creator:Bishop, Matthew T ; Ritchie, Diane L ; Will, Robert G ; Ironside, James W ; Head, Mark W ; Thomson, Val ; Bruce, Moira ; Manson, Jean C
Publisher:United States: Public Library of Science
Journal title:PloS one, 2008-08, Vol.3 (8), p.e2878-e2878
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ArticlesPeer ReviewedFull Text
Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrPSc from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein Misfolding Cyclic Ampli...
Author / Creator: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.
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2023-11, Vol.60 (11), p.6275-6293
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Series 02: Allen & Unwin Further Production files, ca. 1976-1990

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Series 04: Allen & Unwin Further publisher files, ca. 1977-1990

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Series 08: Allen & Unwin cover art, ca. 1980-1990

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Series 01 Part 01: Allen & Unwin Production files. F Sequence, ca. 1980-1990

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

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

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Characterization of variably protease-sensitive prionopathy by capillary electrophoresis

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Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

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Variant CJD: Reflections a Quarter of a Century on

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

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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 evidence of prion di...

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

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A Naturally Occurring Bovine Tauopathy Is Geographically Widespread in the UK

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

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

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

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

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

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No major change in vCJD agent strain after secondary transmission via blood transfusion

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Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrPSc from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein Misfolding Cyclic Ampli...

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