Diane L Ritchie

Diane L Ritchie

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Diane L Ritchie

Diane L Ritchie

Publications by authors named "Diane L Ritchie"

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Neuropathology of Human Prion Diseases.

Prog Mol Biol Transl Sci 2017 3;150:319-339. Epub 2017 Aug 3.

National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, School of Clinical Sciences, University of Edinburgh, Western General Hospital, Edinburgh, United Kingdom. Electronic address:

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http://dx.doi.org/10.1016/bs.pmbts.2017.06.011DOI Listing
May 2018

Prion diseases.

Handb Clin Neurol 2017 ;145:393-403

National CJD Research and Surveillance Unit, Centre for Clinical Brain Sciences, School of Clinical Sciences, University of Edinburgh, Western General Hospital, Edinburgh, United Kingdom.

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http://dx.doi.org/10.1016/B978-0-12-802395-2.00028-6DOI Listing
January 2018

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

Acta Neuropathol 2017 08 27;134(2):221-240. Epub 2017 Mar 27.

National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, Deanery of Clinical Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.

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http://dx.doi.org/10.1007/s00401-017-1703-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508038PMC
August 2017

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

Acta Neuropathol 2017 04 3;133(4):579-595. Epub 2016 Nov 3.

National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, Deanery of Clinical Sciences, The University of Edinburgh, Edinburgh, UK.

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http://dx.doi.org/10.1007/s00401-016-1638-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348565PMC
April 2017

Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes.

J Proteome Res 2016 12 30;15(12):4518-4531. Epub 2016 Sep 30.

Rocky Mountain Laboratories, National Institute of Allergy & Infectious Disease, National Institutes of Health , Hamilton, Montana 59840, United States.

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http://dx.doi.org/10.1021/acs.jproteome.6b00633DOI Listing
December 2016

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

PLoS One 2015 19;10(6):e0129499. Epub 2015 Jun 19.

Animal and Plant Health Agency, Lasswade Veterinary Laboratory, Pentlands Science Park, Bush Loan, Penicuik, Midlothian, Scotland.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0129499PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474601PMC
April 2016

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

Transfusion 2016 Mar 23;56(3):712-21. Epub 2015 Nov 23.

National Institute of Neurological Diseases and Stroke, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1111/trf.13422DOI Listing
March 2016

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

PLoS Pathog 2016 Feb 3;12(2):e1005416. Epub 2016 Feb 3.

Rocky Mountain Laboratories, National Institute of Allergy & Infectious Diseases, National Institutes of Health, Hamilton, Montana, United States of America.

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http://dx.doi.org/10.1371/journal.ppat.1005416DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740439PMC
February 2016

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

Acta Neuropathol Commun 2014 Oct 21;2:152. Epub 2014 Oct 21.

National CJD Research & Surveillance Unit (NCJDRSU), School of Clinical Sciences (Division of Clinical Neurosciences), College of Medicine and Veterinary Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.

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http://dx.doi.org/10.1186/s40478-014-0152-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210614PMC
October 2014

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

Brain 2013 Apr 28;136(Pt 4):1139-45. Epub 2013 Feb 28.

National Creutzfeldt–Jakob Disease Research and Surveillance Unit, University of Edinburgh, Bryan Matthews Building, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.

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https://academic.oup.com/brain/article-lookup/doi/10.1093/br
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http://dx.doi.org/10.1093/brain/awt032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613713PMC
April 2013

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

Brain 2013 Apr;136(Pt 4):1102-15

National Creutzfeldt-Jakob Disease Research & Surveillance Unit, Bryan Matthews Building, Western General Hospital, Edinburgh EH4 2XU, UK.

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http://dx.doi.org/10.1093/brain/aws366DOI Listing
April 2013

Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type mice.

J Gen Virol 2009 Dec 5;90(Pt 12):3075-82. Epub 2009 Aug 5.

National CJD Surveillance Unit, School of Molecular and Clinical Medicine (Pathology), University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.

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http://dx.doi.org/10.1099/vir.0.013227-0DOI Listing
December 2009

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

PLoS One 2008 Aug 6;3(8):e2878. Epub 2008 Aug 6.

National CJD Surveillance Unit, University of Edinburgh, Western General Hospital, Edinburgh, United Kingdom.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0002878PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2478718PMC
August 2008

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease.

J Gen Virol 2007 Mar;88(Pt 3):1068-72

National Creutzfeldt-Jakob Disease Surveillance Unit (NCJDSU) and Division of Pathology, School of Molecular and Clinical Medicine, University of Edinburgh, Western General Hospital, Edinburgh, UK.

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http://dx.doi.org/10.1099/vir.0.81913-0DOI Listing
March 2007

Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study.

BMJ 2006 May 10;332(7551):1186-8. Epub 2006 Apr 10.

National Creutzfeldt-Jakob Disease Surveillance Unit, School of Molecular and Clinical Medicine, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU. [corrected]

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http://dx.doi.org/10.1136/bmj.38804.511644.55DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1463905PMC
May 2006

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

Folia Neuropathol 2005 ;43(4):271-8

National Kreutzfeld-Jakob Disiease Surveillance Unit, Division of Pathology, School of Molecular and Clinical Medicine, University of Edinburgh, Western General Hospital, EH4 2XU, United Kingdom.

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April 2006

Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob disease.

Am J Pathol 2006 Mar;168(3):927-35

National Creutzfeldt-Jakob Disease Surveillance Unit and Division of Pathology, School of Molecular and Clinical Medicine, University of Edinburgh, Western General Hospital, Edinburgh, United Kingdom.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1606529PMC
http://dx.doi.org/10.2353/ajpath.2006.050788DOI Listing
March 2006

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease.

Am J Pathol 2006 Jan;168(1):151-7

National CJD Surveillance Unit, School of Molecular and Clinical Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592651PMC
http://dx.doi.org/10.2353/ajpath.2006.050766DOI Listing
January 2006

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

Lancet 2004 Aug 7-13;364(9433):527-9

National Creutzfeldt-Jakob Disease Surveillance Unit, Division of Pathology, School of Molecular and Clinical Medicine, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU, UK.

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http://dx.doi.org/10.1016/S0140-6736(04)16811-6DOI Listing
August 2004