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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: mcguigan c. 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.
Cognitive dysfunction in early multiple sclerosis: a review.
McNicholas N, O'Connell K, Yap SM, Killeen RP, Hutchinson M, McGuigan C. McNicholas N, et al. Among authors: mcguigan c. QJM. 2018 Jun 1;111(6):359-364. doi: 10.1093/qjmed/hcx070. QJM. 2018. PMID: 28371862 Review.
2017 McDonald diagnostic criteria: A review of the evidence.
McNicholas N, Hutchinson M, McGuigan C, Chataway J. McNicholas N, et al. Among authors: mcguigan c. Mult Scler Relat Disord. 2018 Aug;24:48-54. doi: 10.1016/j.msard.2018.05.011. Epub 2018 Jun 21. Mult Scler Relat Disord. 2018. PMID: 29936325 Review.
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: mcguigan c. Eur Neurol. 2004;51(3):132-7. doi: 10.1159/000077063. Epub 2004 Feb 26. Eur Neurol. 2004. PMID: 14988606
346 results