PAPERS - RESEARCH FRONT: 13

TITLE 1ST AUTHOR YEAR
Prion disease and blood transfusion Flanagan P 1996
Creutzfeldt-Jakob disease - A survey of 14 patients Marchiori PE 1996
Prion disease and anaesthesia. Estebe JP 1997
BSE and human prion disease Harrison PJ 1997
Prion diseases Korczyn AD 1997
Bovine spongiform encephalopathy (BSE): Causes and consequences of a common source epidemic Nathanson N 1997
A prion primer Cashman NR 1997
An overview of the BSE epidemic in the UK Bradley R 1998
Transmission of spongiform encephalopathy through biological products Brown P 1998
Sporadic Creutzfeldt-Jakob disease - A clinico-neuropathological analysis of nine definite cases Costa CMD 1998
Prion diseases in man Ironside JW 1998
Prion protein immunohistochemical staining in the brains of monkeys with transmissible spongiform encephalopathy Baker HF 1998
Retrospective neuropathological review of prion disease in UK haemophilic patients Lee CA 1998
Creutzfeldt-Jakob disease in Sweden Lundberg PO 1998
Submicroscopic immunodetection of PrP in the brain of a patient with a new-variant of Creutzfeldt-Jakob disease Grigoriev V 1999
The transmission of prions to humans Will RG 1999
Pathology of variant Creutzfeldt-Jakob disease Ironside JW 2000
Detection of PrPSc in subclinical BSE with the paraffin-embedded tissue (PET) blot Schulz-Schaeffer WJ 2000
The new variant of Creutzfeldt-Jakob disease Zeidler M 2000
The human transmissible spongiform encephalopathies (TSEs): implications for dental practitioners Porter S 2000
Variant Creutzfeldt-Jakob disease: Immunocytochemical studies and image analysis Nailon WH 2000
vCJD - predicting the future? Hilton DA 2000
Psychiatric features of the new variant Creutzfeldt-Jakob disease. A case report Dervaux A 2001
Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-Jakob disease: Implications for human health Lasmezas CI 2001
Creutzfeldt-Jakob disease (CJD) in a case of suspected chronic heavy metal poisoning Oehmichen M 2001
The many faces of human prion diseases in Belgium and the world Van Everbroeck B 2001
Clinical implications of bovine spongiform encephalopathy MacKnight C 2001
Classical and variant Creutzfeldt-Jakob diseases and their potential impact on the practice of clinical dentistry in Australia Chan SWY 2001
Creutzfeldt-Jakob disease with E200K mutation in Slovakia: Characterization and development Mitrova E 2002
Neuropathology of variant Creutzfeldt-Jakob disease Ironside JW 2002
Profound sex-specific effects on incubation times for transmission of bovine spongiform encephalopathy to mice Abiola OO 2002
Prion diseases: Epidemiology in man Pedersen NS 2002
Blood infectivity in transmissible spongiform encephalopathies Dickmeiss E 2002
Factor VIII and transmissible spongiform encephalopathy: the case for safety Cervenakova L 2002
Psychological versus biological clinical interpretation: A patient with prion disease Solvason HB 2002
Prion diseases Kretzschmar HA 2002
Human prion diseases Kretzschmar HA 2002
Is there a risk of prion disease after the administration of urinary-derived gonadotrophins? Balen A 2002
Sporadic Creutzfeldt-Jakob disease: phenotypic variability Moreno MJ 2002
Use of 14-3-3 in the diagnosis of Creutzfeldt-Jakob disease Green AJE 2002
Acquired prion disease: iatrogenic CJD, variant CJD, kuru Will RG 2003
Projection of Creutzfeldt-Jakob disease frequency based on cadaveric dura transplantation in Japan Hamada C 2003
Monitoring the occurrence of emerging forms of Creutzfeldt-Jakob disease in the United States Belay ED 2003
Variant Creutzfeldt-Jakob disease Ward HJT 2003
Present-day knowledge of BSE and Creutzfeldt-Jakob disease Schatzl HM 2003
Failure of immunocompetitive capillary electrophoresis assay to detect disease-specific prion protein in buffy coat from humans and chimpanzees with Creutzfeldt-Jakob disease Cervenakova L 2003
Sporadic Creutzfeldt-Jakob disease mimicking variant Creutzfeldt-Jakob disease Martindale J 2003
Use and validity of the 14-3-3 protein test in the diagnosis of prion diseases: a 4-year prospective study Diaz RSV 2003
Latrogenic Creutzfeldt-Jakob disease with florid plaques Kretzschmar HA 2003
Variant Creutzfeldt-Jakob disease and its transmission by blood Ironside JW 2003
Neuronal and astrocytic responses involving the serotonergic system in human spongiform encephalopathies Fraser E 2003
Prions and the oral cavity Smith AJ 2003
Prion disease - Possible implications for oral health care Porter SR 2003
Update on prion disease Brandel JP 2003
The neuropsychological profile associated with variant Creutzfeldt-Jakob disease Kapur N 2003
Clinical features of variant Creutzfeldt-Jakob disease Will RG 2004
Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease Ironside JW 2004
Peripheral tissue involvement in sporadic, latrogenic, and variant Creutzfeldt-Jakob disease - An immunohistochemical, quantitative, and biochemical study Head MW 2004
Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion Llewelyn CA 2004
Rationale for diagnosing human prion disease Kovacs GG 2004
Prevalence of lymphoreticular prion protein accumulation in UK tissue samples Hilton DA 2004
Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting Ritchie DL 2004
The modern landscape of transfusion-related iatrogenic Creutzfeldt-Jakob disease and blood screening tests Brown P 2004
Variant Creutzfeldt-Jakob disease: risk of transmission by blood and blood products Ironside JW 2004
Molecular classification of scrapie strains in mice using gene expression profiling Booth S 2004
Working with transmissible spongiform encephalopathy agents Brown P 2005
The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction Peoc'h K 2005
The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease Cordery RJ 2005