1. Association of a null allele of SPRN with variant Creutzfeldt–Jakob disease. Issue 12 (19th September 2008) Authors: Beck, J A; Campbell, T A; Adamson, G; Poulter, M; Uphill, J B; Molou, E; Collinge, J; Mead, S Journal: Journal of medical genetics Issue: Volume 45:Issue 12(2008) Page Start: 813 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. K11 C9orf72 Expansions Are The Most Common Genetic Cause Of Huntington's Disease Phenocopy Presentations In A Uk Cohort. (17th September 2014) Authors: Hensman Moss, DJ; Poulter, M; Beck, J; Polke, JM; Campbell, T; Adamson, G; Hehir, J; Mudanohwo, E; McColgan, P; Wild, EJ; Haworth, A; Sweeney, MG; Houlden, H; Mead, S; Tabrizi, SJ Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 85(2014)Supplement 1 Page Start: A82 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. TREM2 VARIANTS INCREASE RISK OF TYPICAL EARLY-ONSET ALZHEIMER'S DISEASE BUT NOT OF PRION OR FRONTOTEMPORAL DEMENTIA. Issue 8 (9th July 2014) Authors: Slattery, CF; Beck, J; Harper, L; Adamson, G; Abdi, Z; Uphill, J; Campbell, T; Druyeh, R; Mahoney, CJ; Rohrer, JD; Kenny, J; Lowe, J; Leung, KK; Barnes, J; Clegg, SL; Blair, M; Nicholas, JM; Guerreiro, RJ; Rowe, JB; Ponto, C Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 85:Issue 8(2014) Page Start: e3 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗