| Document Date: 2013-11-05 09:38:54
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City Gill / Appleford / / Company Cooper SA / EUROCJD Group / Uitterlinden AG / Diack AB / GE / Oxford University Press / Priola SA / Simmons / Tullo AB / / Continent Europe / / Country Netherlands / Turkey / France / United States / United Kingdom / Scotland / / Event Product Issues / / Facility Hospital Epidemiology / / IndustryTerm plasma products / contaminated plasma products / Brain banking / in vitro cell-free conversion systems / / MedicalCondition Human Prion Diseases / Haik S. Variant Creutzfeldt-Jakob disease / Panencephalopathic Creutzfeldt-Jakob disease / bovine spongiform encephalopathy epizootic / Will R. Variant cjd / sub-clinical variant Creutzfeldt-Jakob disease / Dementia / human prion disease / Familial prion disease / Tagliavini F. Sporadic Creutzfeldt-Jakob disease / sporadic cjd / strain / neurological disorders / Haemophilia / Tagliavini F. MM2-thalamic CreutzfeldtJakob disease / inherited bleeding disorders / sporadic CreutzfeldtJakob disease / prion disease / Iatrogenic Creutzfeldt-Jakob disease / UK sporadic and variant Creutzfeldt-Jakob disease / Human Prion Infection / subclinical variant Creutzfeldt-Jakob disease / CreutzfeldtJakob disease / human genetic transmissible spongiform encephalopathies / French variant Creutzfeldt-Jakob disease epidemic / BMC Infectious Diseases / Kapur N. Variant Creutzfeldt-Jakob disease / variant and sporadic Creutzfeldt-Jakob disease / mitochondrial diseases / sporadic and genetic CreutzfeldtJakob disease / sporadic Creutzfeldt-Jakob disease / Variant CJD infection / Brain Pathology / variant Creutzfeldt-Jakob disease / Will B. Variant CJD / Creutzfeldt-Jakob disease / disease / variant Creutzfeldt-Jakob disease infection / mitrochondrial diseases / observed disease / Speech Apraxia / Hewitt P. Variant Creutzfeldt-Jakob disease / progressive supranuclear palsy / Rudge P. Variant CJD / GerstmannStraussler-Scheinker disease / neurological disease / transmissible spongiform encephalopathies / Movement Disorders / Gerstmann-Straussler-Scheinker disease / variant CJD / Schonberger LB. Iatrogenic Creutzfeldt-Jakob disease / neurodegenerative diseases / probable variant Creutzfeldt-Jakob disease / Mead S. Inherited prion disease / disorders / / MedicalTreatment blood transfusion / surgery / blood transfusions / / NaturalFeature Bishop MT / / Organization Oxford University / / Person Al-Shahi Salman / Arch Dis / Ann Neurol / Pedro Cuesta / Murray K. Creutzfeldt-Jakob / Mead S. Inherited / Barron R. Differential / / Position Bishop MT / Bishop / / Product plasma products / medical instruments / / PublishedMedium Infection Control and Hospital Epidemiology / / RadioStation Molesworth AM / Winstone AM / Richardson AM / Watt / / TVStation Wand / / Technology antibodies / transplantation / stem cells / MRI / prions / /
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ARTICLES BY THE NCJDRSU SINCE[removed]last updated November[removed]Bishop MT, Diack AB, Ritchie DL, Ironside JW, Will RG, Manson JC. Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical