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Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study.
Reiman EM, Arboleda-Velasquez JF, Quiroz YT, Huentelman MJ, Beach TG, Caselli RJ, Chen Y, Su Y, Myers AJ, Hardy J, Paul Vonsattel J, Younkin SG, Bennett DA, De Jager PL, Larson EB, Crane PK, Keene CD, Kamboh MI, Kofler JK, Duque L, Gilbert JR, Gwirtsman HE, Buxbaum JD, Dickson DW, Frosch MP, Ghetti BF, Lunetta KL, Wang LS, Hyman BT, Kukull WA, Foroud T, Haines JL, Mayeux RP, Pericak-Vance MA, Schneider JA, Trojanowski JQ, Farrer LA, Schellenberg GD, Beecham GW, Montine TJ, Jun GR; Alzheimer’s Disease Genetics Consortium. Reiman EM, et al. Among authors: kukull wa. Nat Commun. 2020 Feb 3;11(1):667. doi: 10.1038/s41467-019-14279-8. Nat Commun. 2020. PMID: 32015339 Free PMC article.
Cognitive impairment: dementia and Alzheimer's disease.
Larson EB, Kukull WA, Katzman RL. Larson EB, et al. Among authors: kukull wa. Annu Rev Public Health. 1992;13:431-49. doi: 10.1146/annurev.pu.13.050192.002243. Annu Rev Public Health. 1992. PMID: 1599598 Review.
APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.
Schellenberg GD, Anderson L, O'dahl S, Wisjman EM, Sadovnick AD, Ball MJ, Larson EB, Kukull WA, Martin GM, Roses AD, et al. Schellenberg GD, et al. Among authors: kukull wa. Am J Hum Genet. 1991 Sep;49(3):511-7. Am J Hum Genet. 1991. PMID: 1679288 Free PMC article.
324 results