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Page 1
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
Webb TE, Poulter M, Beck J, Uphill J, Adamson G, Campbell T, Linehan J, Powell C, Brandner S, Pal S, Siddique D, Wadsworth JD, Joiner S, Alner K, Petersen C, Hampson S, Rhymes C, Treacy C, Storey E, Geschwind MD, Nemeth AH, Wroe S, Collinge J, Mead S. Webb TE, et al. Among authors: wroe s. Brain. 2008 Oct;131(Pt 10):2632-46. doi: 10.1093/brain/awn202. Epub 2008 Aug 30. Brain. 2008. PMID: 18757886 Free PMC article.
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation.
Alner K, Hyare H, Mead S, Rudge P, Wroe S, Rohrer JD, Ridgway GR, Ourselin S, Clarkson M, Hunt H, Fox NC, Webb T, Collinge J, Cipolotti L. Alner K, et al. Among authors: wroe s. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1):109-14. doi: 10.1136/jnnp-2011-300167. Epub 2011 Aug 17. J Neurol Neurosurg Psychiatry. 2012. PMID: 21849340
PRION-1 scales analysis supports use of functional outcome measures in prion disease.
Mead S, Ranopa M, Gopalakrishnan GS, Thompson AG, Rudge P, Wroe S, Kennedy A, Hudson F, MacKay A, Darbyshire JH, Collinge J, Walker AS. Mead S, et al. Among authors: wroe s. Neurology. 2011 Nov 1;77(18):1674-83. doi: 10.1212/WNL.0b013e3182364890. Epub 2011 Oct 19. Neurology. 2011. PMID: 22013183 Free PMC article.
Neuroimaging findings in human prion disease.
Macfarlane RG, Wroe SJ, Collinge J, Yousry TA, Jäger HR. Macfarlane RG, et al. Among authors: wroe sj. J Neurol Neurosurg Psychiatry. 2007 Jul;78(7):664-70. doi: 10.1136/jnnp.2006.094821. Epub 2006 Nov 29. J Neurol Neurosurg Psychiatry. 2007. PMID: 17135459 Free PMC article. Review.
151 results