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Number of items: 4.


Mead, S; Uphill, J; Beck, J; Poulter, M; Campbell, T; Lowe, J; Adamson, G; Hummerich, H; Klopp, N; Ruckert, IM; +11 more... Wichmann, HE; Azazi, D; Plagnol, V; Pako, WH; Whitfield, J; Alpers, MP; Whittaker, J; Balding, DJ; Zerr, I; Kretzschmar, H; Collinge, J; (2012) Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Human molecular genetics, 21 (8). pp. 1897-1906. ISSN 0964-6906 DOI: Full text not available from this repository.


Mead, S; Poulter, M; Uphill, J; Beck, J; Whitfield, J; Webb, TEF; Campbell, T; Adamson, G; Deriziotis, P; Tabrizi, SJ; +5 more... Hummerich, H; Verzilli, C; Alpers, MP; Whittaker, JC; Collinge, J; (2009) Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. Lancet neurology, 8 (1). pp. 57-66. ISSN 1474-4422 DOI:


Llewelyn, CA; Hewitt, PE; Knight, RSG; Amar, K; Cousens, S; MacKenzie, J; Will, RG; (2004) Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. Lancet, 363 (9407). pp. 417-421. ISSN 0140-6736 DOI: Full text not available from this repository.


D'Aignaux, JN; Cousens, SN; Smith, PG; (2001) Predictability of the UK variant Creutzfeldt-Jakob disease epidemic. Science (New York, NY), 294 (5547). pp. 1729-31. ISSN 0036-8075 DOI: Full text not available from this repository.

This list was generated on Wed Jul 24 19:02:08 2019 BST.