Browsing by author "Forrest, SL"
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[18F]AV-1451 PET in behavioural variant frontotemporal dementia due to MAPT mutation
Bevan Jones, WR; Cope, TE; Passamonti, L; Fryer, TD; Hong, YT; Aigbirhio, F; Kril, JJ; Forrest, SL; Allinson, K; Coles, JP; Spillantini, MG; Hodges, JR; O'Brien, JT; Rowe, JBPublished 2016-10-18The validation of tau radioligands could improve the diagnosis of frontotemporal lobar degeneration and the assessment of disease-modifying therapies. Here, we demonstrate that binding of the tau radioligand [18F]AV-1451 ...Open AccessArticle -
Expanding the phenotypic associations of globular glial tau subtypes
Burrell, JR; Forrest, SL; Bak, TH; Hodges, JR; Halliday, GM; Kril, JJPublished 2016-04-08Clinicopathologic correlation in non-Alzheimer's tauopathies is variable, despite refinement of pathologic diagnostic criteria. In the present study, the clinical and neuroimaging characteristics of globular glial tauopathy ...Open AccessArticle -
Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies
Forrest, SL; Kril, JJ; Stevens, C; Kwok, JB; Hallupp, M; Kim, W; Huang, Y; McGinley, C; Werka, H; Kiernan, MC; Gotz, J; Spillantini, MG; Hodges, JR; Ittner, LM; Halliday, GMPublished 2017-01-01See Josephs (doi:10.1093/brain/awx367) for a scientific commentary on this article.In many neurodegenerative disorders, familial forms have provided important insights into the pathogenesis of their corresponding sporadic ...Open AccessArticle
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