Mika H Martikainen

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 9

Top Topics

Deep Brain Stimulation

Magnetic Resonance

Top Venues

BMJ neurology open

Case reports in neurological medicine

Wellcome open research

This page only lists publications with an associated author ORCID identifier.

Publications

Mika H Martikainen, Kari Majamaa
Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009-2022: an observational, population-based study. BMJ neurology open 6 (1) (2024)
Sakari Kaasalainen, Harri Arikka, Mika H Martikainen, Valtteri Kaasinen
Novel SLC18A2 Variant in Infantile Dystonia-Parkinsonism Type 2. Case reports in neurological medicine 2024 (2024)
Sakari Kaasalainen, Harri Arikka, Mika H Martikainen, Valtteri Kaasinen
Novel SLC18A2 Variant in Infantile Dystonia-Parkinsonism Type 2. Case reports in neurological medicine 2024 (2024)
Mika H Martikainen, Kari Majamaa
Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009-2022: an observational, population-based study. BMJ neurology open 6 (1) (2024)
Mika H Martikainen, Miika Suomela, Kari Majamaa
Magnetic resonance imaging negative myelopathy in Leber's hereditary optic neuropathy: a case report. BMC neurology 22 (1) (2022)
Mika H Martikainen, Miika Suomela, Kari Majamaa
Magnetic resonance imaging negative myelopathy in Leber's hereditary optic neuropathy: a case report. BMC neurology 22 (1) (2022)
Mika H Martikainen, Miika Suomela, Kari Majamaa
Magnetic resonance imaging negative myelopathy in Leber's hereditary optic neuropathy: a case report. BMC neurology 22 (1) (2022)
Yi Shiau Ng, Laurence A Bindoff, Gráinne S Gorman, Rita Horvath, Thomas Klopstock, Michelangelo Mancuso, Mika H Martikainen, Robert McFarland, Victoria Nesbitt, Robert D S Pitceathly, Andrew M Schaefer, Doug M Turnbull
Consensus-based statements for the management of mitochondrial stroke-like episodes. Wellcome open research 4 (2019)
Laura Kytövuori, Maria Gardberg, Kari Majamaa, Mika H Martikainen
The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype. Brain and behavior 7 (12) (2017)