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Stable low prevalence of Huntington's disease in Finland.
Sipilä JOT, Majamaa K. Sipilä JOT, et al. Among authors: majamaa k. Clin Park Relat Disord. 2023 Apr 28;8:100198. doi: 10.1016/j.prdoa.2023.100198. eCollection 2023. Clin Park Relat Disord. 2023. PMID: 37152417 Free PMC article. No abstract available.
Association of biallelic RFC1 expansion with early-onset Parkinson's disease.
Ylikotila P, Sipilä J, Alapirtti T, Ahmasalo R, Koshimizu E, Miyatake S, Hurme-Niiranen A, Siitonen A, Doi H, Tanaka F, Matsumoto N, Majamaa K, Kytövuori L. Ylikotila P, et al. Among authors: majamaa k. Eur J Neurol. 2023 May;30(5):1256-1261. doi: 10.1111/ene.15717. Epub 2023 Feb 12. Eur J Neurol. 2023. PMID: 36705320
Cognitive impairment is not uncommon in patients with biallelic RFC1 AAGGG repeat expansion, but the expansion is rare in patients with cognitive disease.
Korpioja A, Krüger J, Hurme-Niiranen A, Solje E, Katisko K, Lipponen J, Lehtilahti M, Remes AM, Majamaa K, Kytövuori L. Korpioja A, et al. Among authors: majamaa k. Parkinsonism Relat Disord. 2022 Oct;103:98-101. doi: 10.1016/j.parkreldis.2022.08.034. Epub 2022 Sep 6. Parkinsonism Relat Disord. 2022. PMID: 36088850 Free article.
Association between mitochondrial DNA haplogroups J and K, serum branched-chain amino acids and lowered capability for endurance exercise.
Kiiskilä JM, Hassinen IE, Kettunen J, Kytövuori L, Mikkola I, Härkönen P, Jokelainen JJ, Keinänen-Kiukaanniemi S, Perola M, Majamaa K. Kiiskilä JM, et al. Among authors: majamaa k. BMC Sports Sci Med Rehabil. 2022 May 26;14(1):95. doi: 10.1186/s13102-022-00485-3. BMC Sports Sci Med Rehabil. 2022. PMID: 35619160 Free PMC article.
Biallelic expansion in RFC1 as a rare cause of Parkinson's disease.
Kytövuori L, Sipilä J, Doi H, Hurme-Niiranen A, Siitonen A, Koshimizu E, Miyatake S, Matsumoto N, Tanaka F, Majamaa K. Kytövuori L, et al. Among authors: majamaa k. NPJ Parkinsons Dis. 2022 Jan 10;8(1):6. doi: 10.1038/s41531-021-00275-7. NPJ Parkinsons Dis. 2022. PMID: 35013364 Free PMC article.
219 results