1. 022 Voxelwise analysis of cerebral diffusion tensor imaging in prion diseases. Issue 3 (9th February 2012) Authors: Porter, M C; Hyare, H; De Vita, E; Thompson, A; Lukic, A; Yousry, T; Rudge, P; Mead, S; Collinge, J; Thornton, J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83:Issue 3(2012) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 1130 White matter lesions in familial Alzheimer's disease: evidence for influence of mutation position on amyloid angiopathy?. Issue 3 (9th February 2012) Authors: Ryan, N; Biessels, G; Bastos-Leite, A; Beck, J; Mead, S; Morris, H; Schott, J M; Rossor, M N; Fox, N C Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83:Issue 3(2012) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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) ↗
4. Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation. Issue 11 (28th October 2009) Authors: Rohrer, J D; Beck, J; Warren, J D; King, A; Sarraj, S Al; Holton, J; Revesz, T; Collinge, J; Mead, S Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 80:Issue 11(2009) Page Start: 1297 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation. Issue 1 (17th August 2011) Authors: Alner, K; Hyare, H; Mead, S; Rudge, P; Wroe, S; Rohrer, J D; Ridgway, G R; Ourselin, S; Clarkson, M; Hunt, H; Fox, N C; Webb, T; Collinge, J; Cipolotti, L Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83:Issue 1(2012) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained. Issue 9 (27th August 2010) Authors: Stevens, J C; Beck, J; Lukic, A; Ryan, N; Abbs, S; Collinge, J; Fox, N C; Mead, S Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 82:Issue 9(2011) Page Start: 1054 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. 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) ↗
8. MULTI-PARAMETER MRI ANALYSIS IN THE NATIONAL PRION COHORT. Issue 10 (9th September 2014) Authors: Porter, M-C; De Vita, E; Simpson, I; Franko, E; Bjurstrom, N; Rudge, P; Mead, S; Collinge, J; Thornton, J; Hyare, H Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 85:Issue 10(2014) Page Start: e4 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. PALLIATIVE AND HOSPICE SERVICES IN LONG TERM CARE. (11th November 2018) Authors: Harrison, T; Blozis, S; Dionne-Vahalik, M; Mead, S Journal: Innovation in aging Issue: Volume 2(2018)Supplement 1 Page Start: 152 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. PATU2 Novel truncation mutation of PRNP causes chronic diarrhoea, sensory neuropathy and autonomic failure associated with prion protein deposition in the cerebral blood vessels and small bowel. Issue 11 (22nd October 2010) Authors: Mead, S; Linehan, J; Beck, J; Caine, D; Gandhi, S; Wadsworth, J D F; Joiner, S; Gallujipali, D; Hyare, H; Lees, A; Holton, J; Sandberg, M; Revesz, T; Carswell, C; Warren, J D; Collinge, J; Wood, N Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 81:Issue 11(2010) Page Start: e24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗