Search Results - "Ironside, JW"
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Predicting susceptibility and incubation time of human-to-human transmission of vCJD
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
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
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
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
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
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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Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium
Published in Acta neuropathologica (01-06-2009)“…When 22 members of the BrainNet Europe (BNE) consortium assessed 31 cases with α-synuclein (αS) immunoreactive (IR) pathology applying the consensus protocol…”
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Prevalence of lymphoreticular prion protein accumulation in UK tissue samples
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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Pituitary gland pathology
Published in Journal of clinical pathology (01-08-2003)Get full text
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Assessment of β-amyloid deposits in human brain: a study of the BrainNet Europe Consortium
Published in Acta neuropathologica (01-03-2009)“…β-Amyloid (Aβ) related pathology shows a range of lesions which differ both qualitatively and quantitatively. Pathologists, to date, mainly focused on the…”
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Incidence of variant Creutzfeldt-Jakob disease in the UK
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
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
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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The need to unify neuropathological assessments of vascular alterations in the ageing brain: multicentre survey by the BrainNet Europe consortium
Published in Experimental gerontology (01-11-2012)“…Here, we summarise the results after carrying out a large survey regarding the assessment of vascular alterations, both vessel changes and vascular lesions in…”
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Molecular classification of sporadic Creutzfeldt–Jakob disease
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
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2006)“…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
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
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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Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe Consortium
Published in Neuropathology and applied neurobiology (01-02-2013)“…G. G. Kovacs, A. J. M. Rozemuller, J. C. van Swieten, E. Gelpi, K. Majtenyi, S. Al‐Sarraj, C. Troakes, I. Bódi, A. King, T. Hortobágyi, M. M. Esiri, O…”
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