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A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene.
Olszewska DA, Fearon C, McGuigan C, McVeigh TP, Houlden H, Polke JM, Lawlor B, Coen R, Hutchinson M, Hutton M, Beausang A, Delon I, Brett F, Sevastou I, Seto-Salvia N, de Silva R, Lynch T. Olszewska DA, et al. Among authors: brett f. Neurobiol Aging. 2021 Oct;106:343.e1-343.e8. doi: 10.1016/j.neurobiolaging.2021.05.010. Epub 2021 May 23. Neurobiol Aging. 2021. PMID: 34274155 Free article.
Creutzfeldt-Jakob disease in Ireland: epidemiological aspects 1980-2002.
Horan G, Keohane C, Molloy S, Howley R, Harney M, Heffernan J, McGuigan C, Hutchinson M, Brett F, Farrell M. Horan G, et al. Among authors: brett f. Eur Neurol. 2004;51(3):132-7. doi: 10.1159/000077063. Epub 2004 Feb 26. Eur Neurol. 2004. PMID: 14988606
Suspected factitious hypoglycemia.
Brett F, Beausang A, Tormey W, Curtis M. Brett F, et al. Clin Neuropathol. 2016 Nov/Dec;35(6):393-395. doi: 10.5414/NP300971. Clin Neuropathol. 2016. PMID: 27641434 No abstract available.
Clinically-diagnosed Susac syndrome in a 50-year-old.
Brett FM, Looby S, Fearon C, Widdess-Walsh P. Brett FM, et al. Clin Neuropathol. 2017 Nov/Dec;36(6):288-290. doi: 10.5414/NP301039. Clin Neuropathol. 2017. PMID: 28899478 No abstract available.
138 results