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Longitudinal neuroanatomical and cognitive progression of posterior cortical atrophy.
Firth NC, Primativo S, Marinescu RV, Shakespeare TJ, Suarez-Gonzalez A, Lehmann M, Carton A, Ocal D, Pavisic I, Paterson RW, Slattery CF, Foulkes AJM, Ridha BH, Gil-Néciga E, Oxtoby NP, Young AL, Modat M, Cardoso MJ, Ourselin S, Ryan NS, Miller BL, Rabinovici GD, Warrington EK, Rossor MN, Fox NC, Warren JD, Alexander DC, Schott JM, Yong KXX, Crutch SJ. Firth NC, et al. Among authors: rossor mn. Brain. 2019 Jul 1;142(7):2082-2095. doi: 10.1093/brain/awz136. Brain. 2019. PMID: 31219516 Free PMC article.
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor.
Fox NC, Kennedy AM, Harvey RJ, Lantos PL, Roques PK, Collinge J, Hardy J, Hutton M, Stevens JM, Warrington EK, Rossor MN. Fox NC, et al. Among authors: rossor mn. Brain. 1997 Mar;120 ( Pt 3):491-501. doi: 10.1093/brain/120.3.491. Brain. 1997. PMID: 9126060
468 results