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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: stevens jm. Brain. 1997 Mar;120 ( Pt 3):491-501. doi: 10.1093/brain/120.3.491. Brain. 1997. PMID: 9126060
The clinical profile of right temporal lobe atrophy.
Chan D, Anderson V, Pijnenburg Y, Whitwell J, Barnes J, Scahill R, Stevens JM, Barkhof F, Scheltens P, Rossor MN, Fox NC. Chan D, et al. Among authors: stevens jm. Brain. 2009 May;132(Pt 5):1287-98. doi: 10.1093/brain/awp037. Epub 2009 Mar 18. Brain. 2009. PMID: 19297506
367 results