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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. Brain. 2008 Oct;131(Pt 10):2632-46. doi: 10.1093/brain/awn202. Epub 2008 Aug 30. Brain. 2008. PMID: 18757886 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.
Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1.
Carswell C, Rañopa M, Pal S, Macfarlane R, Siddique D, Thomas D, Webb T, Wroe S, Walker S, Darbyshire J, Collinge J, Mead S, Rudge P. Carswell C, et al. Dement Geriatr Cogn Dis Extra. 2012 Jan;2(1):286-97. doi: 10.1159/000339730. Epub 2012 Aug 8. Dement Geriatr Cogn Dis Extra. 2012. PMID: 22962552 Free PMC article.
54 results