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Apolipoprotein e genotype modifies the phenotype of Alzheimer disease.
Schott JM, Ridha BH, Crutch SJ, Healy DG, Uphill JB, Warrington EK, Rossor MN, Fox NC. Schott JM, et al. Among authors: warrington ek. Arch Neurol. 2006 Jan;63(1):155-6. doi: 10.1001/archneur.63.1.155. Arch Neurol. 2006. PMID: 16401755 No abstract available.
Sporadic and familial dementia with ubiquitin-positive tau-negative inclusions: clinical features of one histopathological abnormality underlying frontotemporal lobar degeneration.
Godbolt AK, Josephs KA, Revesz T, Warrington EK, Lantos P, King A, Fox NC, Al Sarraj S, Holton J, Cipolotti L, Khan MN, Rossor MN. Godbolt AK, et al. Among authors: warrington ek. Arch Neurol. 2005 Jul;62(7):1097-101. doi: 10.1001/archneur.62.7.1097. Arch Neurol. 2005. PMID: 16009765
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.
Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, Rossor MN, Collinge J, Mead S. Beck J, et al. Among authors: warrington ek. Brain. 2008 Mar;131(Pt 3):706-20. doi: 10.1093/brain/awm320. Epub 2008 Jan 29. Brain. 2008. PMID: 18234697 Free PMC article.
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: warrington ek. Brain. 2019 Jul 1;142(7):2082-2095. doi: 10.1093/brain/awz136. Brain. 2019. PMID: 31219516 Free PMC article.
236 results