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Page 1
Serum neurofilament light in familial Alzheimer disease: A marker of early neurodegeneration.
Weston PSJ, Poole T, Ryan NS, Nair A, Liang Y, Macpherson K, Druyeh R, Malone IB, Ahsan RL, Pemberton H, Klimova J, Mead S, Blennow K, Rossor MN, Schott JM, Zetterberg H, Fox NC. Weston PSJ, et al. Neurology. 2017 Nov 21;89(21):2167-2175. doi: 10.1212/WNL.0000000000004667. Epub 2017 Oct 25. Neurology. 2017. PMID: 29070659 Free PMC article.
Visuomotor integration deficits are common to familial and sporadic preclinical Alzheimer's disease.
Lu K, Nicholas JM, Weston PSJ, Stout JC, O'Regan AM, James SN, Buchanan SM, Lane CA, Parker TD, Keuss SE, Keshavan A, Murray-Smith H, Cash DM, Sudre CH, Malone IB, Coath W, Wong A, Richards M, Henley SMD, Fox NC, Schott JM, Crutch SJ. Lu K, et al. Among authors: weston psj. Brain Commun. 2021 Jan 25;3(1):fcab003. doi: 10.1093/braincomms/fcab003. eCollection 2021. Brain Commun. 2021. PMID: 33615219 Free PMC article.
Plasma amyloid-β ratios in autosomal dominant Alzheimer's disease: the influence of genotype.
O'Connor A, Pannee J, Poole T, Arber C, Portelius E, Swift IJ, Heslegrave AJ, Abel E, Willumsen N, Rice H, Weston PSJ, Ryan NS, Polke JM, Nicholas JM, Mead S, Wray S, Chávez-Gutiérrez L, Frost C, Blennow K, Zetterberg H, Fox NC. O'Connor A, et al. Among authors: weston psj. Brain. 2021 Nov 29;144(10):2964-2970. doi: 10.1093/brain/awab166. Brain. 2021. PMID: 33892504 Free PMC article.
[No title available]
[No authors listed] [No authors listed] PMID: 39112071
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series.
Ryan NS, Nicholas JM, Weston PSJ, Liang Y, Lashley T, Guerreiro R, Adamson G, Kenny J, Beck J, Chavez-Gutierrez L, de Strooper B, Revesz T, Holton J, Mead S, Rossor MN, Fox NC. Ryan NS, et al. Among authors: weston psj. Lancet Neurol. 2016 Dec;15(13):1326-1335. doi: 10.1016/S1474-4422(16)30193-4. Epub 2016 Oct 21. Lancet Neurol. 2016. PMID: 27777022 Free article.
31 results