Stable low prevalence of Huntington’s disease in Finland by Jussi O.T. Sipilä, Kari Majamaa

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Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009–2022: an observational, population-based study by Kari Majamaa, Mika H Martikainen

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Neurological manifestations in adult patients with the m.3243A>G variant in mitochondrial DNA by Kari Majamaa, Mikko Kärppä, Jukka S Moilanen

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Relative contribution of comorbid diseases to health-related quality of life in patients with Parkinson’s disease by Maija-Helena Keränen, Laura Kytövuori, Juha Huhtakangas, Mikko Kärppä, Kari Majamaa

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A severe neurodegenerative disease with Lewy bodies and a mutation in the glucocerebrosidase gene by Jussi O. T. Sipilä, Laura Kytövuori, Tuomas Rauramaa, Hugo Rauhamaa, Valtteri Kaasinen, Kari Majamaa

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An Unusual Developmental Profile of Salla Disease in a Patient with the SallaFIN Mutation by Liisa E. Paavola, Anne M. Remes, Pirkko H. Sonninen, Vesa V. Kiviniemi, Tapio T. Korhonen, Kari Majamaa

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Biallelic expansion in RFC1 as a rare cause of Parkinson’s disease by Laura Kytövuori, Jussi Sipilä, Hiroshi Doi, Anri Hurme-Niiranen, Ari Siitonen, Eriko Koshimizu, Satoko Miyatake, Naomichi Matsumoto, Fumiaki Tanaka, Kari Majamaa

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