Electrochemical methods for the removal of anionic contaminants from water – A review von Pulkka, Susanna, Martikainen, Mika, Bhatnagar, Amit, Sillanpää, Mika

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Magnetic resonance imaging negative myelopathy in Leber's hereditary optic neuropathy: a case report von Martikainen, Mika H, Suomela, Miika, Majamaa, Kari

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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease von Jokela, Manu, Karhu, Jari, Nurminen, Janne, Martikainen, Mika H.

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

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Deep brain stimulation for monogenic Parkinson’s disease: a systematic review von Kuusimäki, Tomi, Korpela, Jaana, Pekkonen, Eero, Martikainen, Mika H., Antonini, Angelo, Kaasinen, Valtteri

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A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism von Kytövuori, Laura, Lipponen, Joonas, Rusanen, Harri, Komulainen, Tuomas, Martikainen, Mika H., Majamaa, Kari

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Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease von Martikainen, Mika H, Ng, Yi Shiau, Gorman, Gráinne S, Alston, Charlotte L, Blakely, Emma L, Schaefer, Andrew M, Chinnery, Patrick F, Burn, David J, Taylor, Robert W, McFarland, Robert, Turnbull, Doug M

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Novel SLC18A2 Variant in Infantile Dystonia-Parkinsonism Type 2 von Kaasalainen, Sakari, Arikka, Harri, Martikainen, Mika H., Kaasinen, Valtteri

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Novel GJB1 mutation causing adult-onset Charcot–Marie–Tooth disease in a female patient von Martikainen, Mika H, Majamaa, Kari

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Consensus-based statements for the management of mitochondrial stroke-like episodes von Ng, Yi Shiau, Bindoff, Laurence A, Gorman, Gráinne S, Horvath, Rita, Klopstock, Thomas, Mancuso, Michelangelo, Martikainen, Mika H, Mcfarland, Robert, Nesbitt, Victoria, Pitceathly, Robert D S, Schaefer, Andrew M, Turnbull, Doug M

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Pathogenic variants in MT‐ATP6: A United Kingdom–based mitochondrial disease cohort study von Ng, Yi Shiau, Martikainen, Mika H., Gorman, Gráinne S., Blain, Alasdair, Bugiardini, Enrico, Bunting, Apphia, Schaefer, Andrew M., Alston, Charlotte L., Blakely, Emma L., Sharma, Sunil, Hughes, Imelda, Lim, Albert, de Goede, Christian, McEntagart, Meriel, Spinty, Stefan, Horrocks, Iain, Roberts, Mark, Woodward, Cathy E., Chinnery, Patrick F., Horvath, Rita, Nesbitt, Victoria, Fratter, Carl, Poulton, Joanna, Hanna, Michael G., Pitceathly, Robert D. S., Taylor, Robert W., Turnbull, Doug M., McFarland, Robert

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Impaired information-processing speed and working memory in leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) and DARS2 mutations: a report... von Martikainen, Mika H., Ellfolk, Ulla, Majamaa, Kari

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Decreased male reproductive success in association with mitochondrial dysfunction von Martikainen, Mika H, Grady, John P, Ng, Yi Shiau, Alston, Charlotte L, Gorman, Grainne S, Taylor, Robert W, McFarland, Robert, Turnbull, Doug M

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Successful treatment of POLG-related mitochondrial epilepsy with antiepileptic drugs and low glycaemic index diet von Martikainen, Mika H., Päivärinta, Markku, Jääskeläinen, Satu, Majamaa, Kari

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Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutation von Martikainen, Mika H, Päivärinta, Markku, Hietala, Marja, Kaasinen, Valtteri

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Spectrum of Movement Disorders in Mitochondrial Disorders–Reply von Martikainen, Mika H, Burn, David J, Turnbull, Doug M

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SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population von Pasanen, Petra, Palin, Eino, Pohjolan-Pirhonen, Risto, Pöyhönen, Minna, Rinne, Juha O, Päivärinta, Markku, Martikainen, Mika H, Kaasinen, Valtteri, Hietala, Marja, Gardberg, Maria, Saukkonen, Anna Maija, Eerola-Rautio, Johanna, Kaakkola, Seppo, Lyytinen, Jukka, Tienari, Pentti J, Paetau, Anders, Suomalainen, Anu, Myllykangas, Liisa

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Mitochondrial DNA variation in sudden cardiac death: a population-based study von Kytövuori, Laura, Junttila, Juhani, Huikuri, Heikki, Keinänen-Kiukaanniemi, Sirkka, Majamaa, Kari, Martikainen, Mika H.

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Validation of the Finnish Version of the Unified Dyskinesia Rating Scale von Kaasinen, Valtteri, Scheperjans, Filip, Kärppä, Mikko, Korpela, Jaana, Brück, Anna, Sipilä, Jussi O.T., Joutsa, Juho, Järvelä, Juha, Eerola-Rautio, Johanna, Martikainen, Mika H., Airaksinen, Katja, Stebbins, Glenn T., Martinez-Martin, Pablo, Goetz, Christopher G., Lin, Jeffrey, Luo, Sheng, Pekkonen, Eero

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The diagnosis of posterior reversible encephalopathy syndrome von Ng, Yi Shiau, Gorman, Grainne S, Turnbull, Doug M, Martikainen, Mika H

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