Mutation m.15923A>G in the MT-TT gene causes mild myopathy – case report of an adult-onset phenotype

by Mikko Kärppä, Laura Kytövuori, Markku Saari, Kari Majamaa
Published 2018-09-01

Amyloid myopathy: a diagnostic challenge

by Heli Tuomaala, Mikko Kärppä, Hannu Tuominen, Anne M. Remes
Published 2009-08-01

Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder

by Laura Kytövuori, Mikko Kärppä, Hannu Tuominen, Johanna Uusimaa, Markku Saari, Reetta Hinttala, Kari Majamaa
Published 2017-05-01

Efficacy and safety of fremanezumab in patients with migraine and inadequate response to prior preventive treatment: subgroup analyses by country of a randomized, placebo-controlle...

by Egilius L. H. Spierings, Mikko Kärppä, Xiaoping Ning, Joshua M. Cohen, Verena Ramirez Campos, Ronghua Yang, Uwe Reuter
Published 2021-04-01