Search Results - "Ironside, JW"

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    Predicting susceptibility and incubation time of human-to-human transmission of vCJD by Bishop, M T, Hart, P, Aitchison, L, Baybutt, H N, Plinston, C, Thomson, V, Tuzi, N L, Head, M W, Ironside, J W, Will, R G, Manson, J C

    Published in Lancet neurology (01-05-2006)
    “…Identification of possible transmission of variant Creutzfeldt-Jakob disease (vCJD) via blood transfusion has caused concern over spread of the disease within…”
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    Review: Creutzfeldt-Jakob disease by Ironside, J W

    Published in Brain pathology (Zurich, Switzerland) (01-10-1996)
    “…The clinicopathological spectrum of Creutzfeldt-Jakob disease has recently been extended by the identification of an apparently new variant of this disorder in…”
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    Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues by Bruce, ME, McConnell, I, Will, RG, Ironside, JW

    Published in The Lancet (British edition) (21-07-2001)
    “…Abnormal accumulations of prion protein (PrP) can be detected in the spleen, lymph nodes, and tonsils of patients with variant Creutzfeldt-Jakob disease…”
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    In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPSc by Jones, M, Peden, AH, Prowse, CV, Gröner, A, Manson, JC, Turner, ML, Ironside, JW, MacGregor, IR, Head, MW

    Published in The Journal of pathology (01-09-2007)
    “…Variant Creutzfeldt-Jakob disease (vCJD) poses a serious risk of secondary transmission and the need to detect infectivity in asymptomatic individuals is…”
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    Tissue and organ donation for research in forensic pathology: the MRC Sudden Death Brain and Tissue Bank by Millar, T, Walker, R, Arango, J.C, Ironside, JW, Harrison, DJ, MacIntyre, DJ, Blackwood, D, Smith, C, Bell, JE

    Published in The Journal of pathology (01-12-2007)
    “…Novel methodological approaches to the investigation of brain and non-central nervous system disorders have led to increased demand for well-characterized,…”
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    Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient by Peden, Alexander H, Head, Mark W, Diane, L Ritchie, Jeanne, E Bell, James, W Ironside

    Published in The Lancet (British edition) (07-08-2004)
    “…We report a case of preclinical variant Creutzfeldt-Jakob disease (vCJD) in a patient who died from a non-neurological disorder 5 years after receiving a blood…”
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    Prevalence of lymphoreticular prion protein accumulation in UK tissue samples by Hilton, David A, Ghani, Azra C, Conyers, Lisa, Edwards, Philip, McCardle, Linda, Ritchie, Diane, Penney, Mark, Hegazy, Doha, Ironside, James W

    Published in The Journal of pathology (01-07-2004)
    “…This study aims to provide an estimate of the number of individuals in the UK who may be incubating variant Creutzfeldt‐Jakob disease and at risk of causing…”
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    Incidence of variant Creutzfeldt-Jakob disease in the UK by Andrews, NJ, Farrington, CP, Cousens, SN, Smith, PG, Ward, H, Knight, RSG, Ironside, JW, Will, RG

    Published in The Lancet (British edition) (05-08-2000)
    “…The number of deaths from variant CJD (vCJD) in the UK increased in the last quarter of 1998, although numbers were lower in subsequent quarters. We analysed…”
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    Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study by Ironside, James W, Bishop, Matthew T, Connolly, Kelly, Hegazy, Doha, Lowrie, Suzanne, Grice, Margaret Le, Ritchie, Diane L, McCardle, Linda M, Hilton, David A

    Published in BMJ (20-05-2006)
    “…Abstract Objective To perform prion protein gene (PRNP) codon 129 analysis in DNA extracted from appendix tissue samples that had tested positive for disease…”
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    Prion Protein Accumulation and Neuroprotection in Hypoxic Brain Damage by McLennan, Neil F., Brennan, Paul M., McNeill, Alisdair, Davies, Ioan, Fotheringham, Andrew, Rennison, Kathleen A., Ritchie, Diane, Brannan, Francis, Head, Mark W., Ironside, James W., Williams, Alun, Bell, Jeanne E.

    Published in The American journal of pathology (01-07-2004)
    “…The function of the normal conformational isoform of prion protein, PrP C, remains unclear although lines of research have suggested a role in the cellular…”
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    Molecular classification of sporadic Creutzfeldt–Jakob disease by Hill, Andrew F., Joiner, Susan, Wadsworth, Jonathan D. F., Sidle, Katie C. L., Bell, Jeanne E., Budka, Herbert, Ironside, James W., Collinge, John

    Published in Brain (London, England : 1878) (01-06-2003)
    “…According to the protein‐only hypothesis of prion propagation, an abnormal isoform (designated PrPSc) of the cellular prion protein (PrPC) is the principal or…”
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    Variant Creutzfeldt-Jakob disease: risk of transmission by blood transfusion and blood therapies by IRONSIDE, J. W.

    “…In the last decade, a new variant of the human prion disease Creutzfeldt–Jakob disease (now known as variant CJD or vCJD) was identified and causally linked to…”
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    Diagnosing Variant Creutzfeldt-Jakob Disease with the Pulvinar Sign: MR Imaging Findings in 86 Neuropathologically Confirmed Cases by Collie, Donald A, Summers, David M, Sellar, Robin J, Ironside, James W, Cooper, Sarah, Zeidler, Martin, Knight, Richard, Will, Robert G

    Published in American journal of neuroradiology : AJNR (01-09-2003)
    “…Variant Creutzfeldt-Jakob disease (vCJD) is a rare but important cause of dementia and death in young patients and is causally linked to bovine spongiform…”
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    The accuracy of meningioma grading: a 10-year retrospective audit by Willis, J., Smith, C., Ironside, J. W., Erridge, S., Whittle, I. R., Everington, D.

    Published in Neuropathology and applied neurobiology (01-04-2005)
    “…Although descriptive classifications of meningioma subtypes are well established, there has been inconsistency in the categorization of meningiomas into…”
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