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British Medical Bulletin|October 3, 2003
Acquired prion disease: iatrogenic CJD, variant CJD, kuruRobert G WillSwiss Medical Weekly|December 31, 2015
The end of the BSE saga: do we still need surveillance for human prion diseases?Herbert Budka, Robert G WillComptes Rendus Biologies|February 28, 2002
Predicting the size of the vCJD epidemic in FranceAnnick Alpérovitch, Robert G WillCold Spring Harbor Perspectives in Medicine|October 30, 2016
Sporadic and Infectious Human Prion DiseasesRobert G Will, James W IronsideJournal of the Royal Society, Interface|February 9, 2007
Is there the potential for an epidemic of variant Creutzfeldt-Jakob disease via blood transfusion in the UK?Paul Clarke, Robert G Will, Azra C GhaniProceedings of the National Academy of Sciences of the United States of America|June 16, 2010
Defining sporadic Creutzfeldt-Jakob disease strains and their transmission propertiesMatthew T Bishop, Robert G Will, Jean C MansonBMJ (Clinical Research Ed.)|June 22, 2002
First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological featuresMichael D Spencer, Richard S G Knight, Robert G WillEmerging Infectious Diseases|October 24, 2007
Source of variant Creutzfeldt-Jakob disease outside United KingdomPascual Sanchez-Juan, Simon N Cousens, Robert G Will, et al.Health & Social Care in the Community|July 18, 2002
Variant Creutzfeldt-Jakob disease: costs borne by familiesSusan Myles, Margaret J Douglas, Hester J T Ward, et al.Neuroepidemiology|March 21, 2009
Survival and re-operation rates after neurosurgical procedures in Scotland: implications for targeted surveillance of sub-clinical variant Creutzfeldt-Jakob diseaseSheila M Bird, Elizabeth L C Merrall, Hester J T Ward, et al.Pageof 5