L. McCardle

发表

Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent

S. Cousens, H. Fraser, I. Mcconnell, 1997, Nature.

Neuropathological phenotype and ‘prion protein’ genotype correlation in sporadic Creutzfeldt-Jakob disease

R. Lathe, J. Bell, O. Windl, 1994, Neuroscience Letters.

Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study.

W. Nailon, J. Ironside, M. Bishop, 2004, The American journal of pathology.

Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease.

J. Ironside, L. McCardle, M. Head, 2003, Investigative ophthalmology & visual science.

Immunohistochemistry for the Prion Protein: Comparison of Different Monoclonal Antibodies in Human Prion Disease Subtypes

H. Budka, J. Hainfellner, J. Ironside, 2002, Brain pathology.

Pathological diagnosis of variant Creutzfeldt‐Jakob disease

J. Ironside, A. Horsburgh, J. Ironside, 2002, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

Prion protein immunocytochemistry – UK five centre consensus report

P. Lantos, I. Allen, J. Lowe, 1997, Neuropathology and applied neurobiology.

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

J. Ironside, N. Andrews, O. N. Gill, 2009, BMJ : British Medical Journal.

Prevalence of lymphoreticular prion protein accumulation in UK tissue samples

Mark Penney, A. Ghani, J. Ironside, 2004, The Journal of pathology.

Disease‐associated prion protein is not detectable in human systemic amyloid deposits

M. Pepys, P. Hawkins, G. Tennent, 2007, The Journal of pathology.

The Detection of Prion Protein in CJD

L. McCardle, Margaret Le Grice, S. Lowrie, 2008 .

Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophilia

S. Love, S. Cousens, J. Ironside, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

Ubiquitin immunocytochemistry in human spongiform encephalopathies

J. Bell, J. Ironside, L. McCardle, 1993, Neuropathology and applied neurobiology.

A new variant of Creutzfeldt-Jakob disease: neuropathological and clinical features.

J. Bell, J. Ironside, R. Will, 1996, Cold Spring Harbor symposia on quantitative biology.

Ultrastructural analysis of the florid plaque in variant Creutzfeldt-Jakob disease.

P. Liberski, J. Ironside, L. McCardle, 2000, Folia neuropathologica.

Prion protein heterogeneity in sporadic but not variant Creutzfeldt–Jakob disease: U.K. cases 1991–2002

J. Ironside, M. Bishop, R. Will, 2004, Annals of neurology.

Laboratory diagnosis of variant Creutzfeldt–Jakob disease

R. Will, J. Ironside, L. McCardle, 2000, Histopathology.

Neuropathology of variant Creutzfeldt-Jakob disease.

J. Ironside, L. McCardle, M. Head, 2002, Acta neurobiologiae experimentalis.

Protection of personnel and environment against Creutzfeldt-Jakob disease in pathology laboratories.

J. Ironside, L. McCardle, N. Kopp, 1999, Clinical and experimental pathology.

Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizootic

J. Linehan, S. Brandner, M. Simmons, 2020, Acta Neuropathologica.

Minimise transmission risk of CJD and vCJD in healthcare settings. Report on the Prevention of CJD and vCJD by Advisory Committee on Dangerous Pathogens' Transmission Spongiform Encephalopathy (ACDP TSE) Subgroup.

D. Jeffries, R. Cumming, A. Fraise, 2015 .

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

James W Ironside, K. Connolly, J. Ironside, 2006, BMJ : British Medical Journal.

Retrospective study of prion-protein accumulation in tonsil and appendix tissues

A. Ghani, J. Ironside, L. McCardle, 2000, The Lancet.

Accumulation of prion protein in tonsil and appendix: review of tissue samples

A. Ghani, J. Ironside, L. McCardle, 2002, BMJ : British Medical Journal.

Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt–Jakob disease

C. Wiley, J. Ironside, L. McCardle, 2004, Journal of Clinical Pathology.

Variant Creutzfeldt-Jakob Disease

R. Will, L. McCardle, Margaret Le Grice, 2005, Transfusion Medicine and Hemotherapy.

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

L. McCardle, P. Edwards, C. Kelly, 2009, BMJ : British Medical Journal.