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Variant Creutzfeldt-Jakob Disease (vCJD) and Transfusion 
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Associations-Organizations  

 

 Journals 

Clewley JP, et al. Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey. BMJ 2009 May21;338:b1442.

Kaski D, et al. Variant CJD in an individual heterozygous for PRNP codon 129. The Lancet 2009 Dec 19;374(9707): 2128.

Pocchiari M. Prevalence of vCJD in the UK. (editorial) BMJ 2009 May 21;338:b435.

Lefrère J-J, Hewitt P. From mad cows to sensible blood transfusion: the risk of prion transmission by labile blood components in the United Kingdom and in France. Transfusion 2009; 49(4):797812.

Coste J, Prowse C, Eglin R, Fang C; for the Subgroup on TSE. A report on transmissible spongiform encephalopathies and transfusion safety. Vox Sang 2009 Feb 10. [Epub ahead of print]

Dietz K, et al. Blood transfusion and spread of variant Creutzfeldt-Jakob disease. Emerging Infectious Diseases 2007 Jan; 13(1).

Editors. Fourth case of transfusion-associated vCJD infection in the United Kingdom.Euro Surveill. 2007 Jan 18;12(1).

Houston F, McCutcheon S, Goldmann W, Chong A, Foster J, Siso S, et al. Prion diseases are efficiently transmitted by blood transfusion in sheep. Blood 2008 Jul 22. [Epub ahead of print]

Turner ML, Ludlam CA. An update on the assessment and management of the risk of transmission of variant Creutzfeldt-Jakob disease by blood and plasma products. Br J Haematol. 2009 Jan;144(1):14–23.

 

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