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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. Among authors: pal 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.
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. Among authors: pal s. 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.
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.
Hermann P, Appleby B, Brandel JP, Caughey B, Collins S, Geschwind MD, Green A, Haïk S, Kovacs GG, Ladogana A, Llorens F, Mead S, Nishida N, Pal S, Parchi P, Pocchiari M, Satoh K, Zanusso G, Zerr I. Hermann P, et al. Among authors: pal s. Lancet Neurol. 2021 Mar;20(3):235-246. doi: 10.1016/S1474-4422(20)30477-4. Lancet Neurol. 2021. PMID: 33609480 Free PMC article. Review.
The importance of ongoing international surveillance for Creutzfeldt-Jakob disease.
Watson N, Brandel JP, Green A, Hermann P, Ladogana A, Lindsay T, Mackenzie J, Pocchiari M, Smith C, Zerr I, Pal S. Watson N, et al. Among authors: pal s. Nat Rev Neurol. 2021 Jun;17(6):362-379. doi: 10.1038/s41582-021-00488-7. Epub 2021 May 10. Nat Rev Neurol. 2021. PMID: 33972773 Free PMC article. Review.
4,701 results