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Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations.
Sakae N, Roemer SF, Bieniek KF, Murray ME, Baker MC, Kasanuki K, Graff-Radford NR, Petrucelli L, Van Blitterswijk M, Rademakers R, Dickson DW. Sakae N, et al. Among authors: roemer sf. Ann Clin Transl Neurol. 2019 Sep;6(9):1782-1796. doi: 10.1002/acn3.50875. Epub 2019 Aug 25. Ann Clin Transl Neurol. 2019. PMID: 31448566 Free PMC article.
Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease.
Valentino RR, Heckman MG, Johnson PW, Baker MC, Soto-Beasley AI, Walton RL, Koga S, Roemer SF, Suh E, Uitti RJ, Trojanowski JQ, Grossman M, Van Deerlin VM, Rademakers R, Wszolek ZK, Dickson DW, Ross OA. Valentino RR, et al. Among authors: roemer sf. Neurology. 2021 Mar 30;96(13):e1755-e1760. doi: 10.1212/WNL.0000000000011649. Epub 2021 Feb 10. Neurology. 2021. PMID: 33568542 Free PMC article.
Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficits.
Rademakers R, Nicholson AM, Ren Y, Koga S, Nguyen HP, Brooks M, Qiao W, Quicksall ZS, Matchett B, Perkerson RB, Kurti A, Castanedes-Casey M, Phillips V, Librero AL, Fernandez De Castro CH, Baker MC, Roemer SF, Murray ME, Asmann Y, Fryer JD, Bu G, Dickson DW, Zhou X. Rademakers R, et al. Among authors: roemer sf. Brain Pathol. 2021 May;31(3):e12945. doi: 10.1111/bpa.12945. Epub 2021 Mar 11. Brain Pathol. 2021. PMID: 33709463 Free PMC article.
Rainwater Charitable Foundation criteria for the neuropathologic diagnosis of progressive supranuclear palsy.
Roemer SF, Grinberg LT, Crary JF, Seeley WW, McKee AC, Kovacs GG, Beach TG, Duyckaerts C, Ferrer IA, Gelpi E, Lee EB, Revesz T, White CL 3rd, Yoshida M, Pereira FL, Whitney K, Ghayal NB, Dickson DW. Roemer SF, et al. Acta Neuropathol. 2022 Oct;144(4):603-614. doi: 10.1007/s00401-022-02479-4. Epub 2022 Aug 10. Acta Neuropathol. 2022. PMID: 35947184 Free PMC article.
25 results