Impact of age and sex on the efficacy of fremanezumab in patients with difficult-to-treat migraine: results of the randomized, placebo-controlled, phase 3b FOCUS study
MaassenVanDenBrink, Antoinette, Terwindt, Gisela M., Cohen, Joshua M., Barash, Steve, Campos, Verena Ramirez, Galic, Maja, Ning, Xiaoping, Kärppä, Mikko
Published in Journal of headache and pain (18.12.2021)
Published in Journal of headache and pain (18.12.2021)
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Efficacy and safety of fremanezumab in patients with migraine and inadequate response to prior preventive treatment: subgroup analyses by country of a randomized, placebo-controlled trial
Spierings, Egilius L. H., Kärppä, Mikko, Ning, Xiaoping, Cohen, Joshua M., Campos, Verena Ramirez, Yang, Ronghua, Reuter, Uwe
Published in Journal of headache and pain (16.04.2021)
Published in Journal of headache and pain (16.04.2021)
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Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study
Marttila, Maria, Kytövuori, Laura, Helisalmi, Seppo, Kallio, Mika, Laitinen, Marjo, Hiltunen, Mikko, Kärppä, Mikko, Majamaa, Kari
Published in Neuroepidemiology (01.01.2017)
Published in Neuroepidemiology (01.01.2017)
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Journal Article
Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder
Kytövuori, Laura, Kärppä, Mikko, Tuominen, Hannu, Uusimaa, Johanna, Saari, Markku, Hinttala, Reetta, Majamaa, Kari
Published in BMC neurology (18.05.2017)
Published in BMC neurology (18.05.2017)
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Journal Article
Hereditary myopathy with early respiratory failure: occurrence in various populations
Palmio, Johanna, Evilä, Anni, Chapon, Françoise, Tasca, Giorgio, Xiang, Fengqing, Brådvik, Björn, Eymard, Bruno, Echaniz-Laguna, Andoni, Laporte, Jocelyn, Kärppä, Mikko, Mahjneh, Ibrahim, Quinlivan, Rosaline, Laforêt, Pascal, Damian, Maxwell, Berardo, Andres, Taratuto, Ana Lia, Bueri, Jose Antonio, Tommiska, Johanna, Raivio, Taneli, Tuerk, Matthias, Gölitz, Philipp, Chevessier, Frederic, Sewry, Caroline, Norwood, Fiona, Hedberg, Carola, Schröder, Rolf, Edström, Lars, Oldfors, Anders, Hackman, Peter, Udd, Bjarne
Published in Journal of neurology, neurosurgery and psychiatry (01.03.2014)
Published in Journal of neurology, neurosurgery and psychiatry (01.03.2014)
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Journal Article
Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish family
Palmio, Johanna, Kärppä, Mikko, Baumann, Peter, Penttilä, Sini, Moilanen, Jukka, Udd, Bjarne
Published in Clinical case reports (01.12.2016)
Published in Clinical case reports (01.12.2016)
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Journal Article
Feasibility and patient acceptability of a commercially available wearable and a smart phone application in identification of motor states in parkinson's disease
Liikkanen, Sammeli, Sinkkonen, Janne, Suorsa, Joni, Kaasinen, Valtteri, Pekkonen, Eero, Kärppä, Mikko, Scheperjans, Filip, Huttunen, Teppo, Sarapohja, Toni, Pesonen, Ullamari, Kuoppamäki, Mikko, Keränen, Tapani
Published in PLOS digital health (01.04.2023)
Published in PLOS digital health (01.04.2023)
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Long-term efficacy and tolerability of lemborexant compared with placebo in adults with insomnia disorder: results from the phase 3 randomized clinical trial SUNRISE 2
Kärppä, Mikko, Yardley, Jane, Pinner, Kate, Filippov, Gleb, Zammit, Gary, Moline, Margaret, Perdomo, Carlos, Inoue, Yuichi, Ishikawa, Kohei, Kubota, Naoki
Published in Sleep (New York, N.Y.) (01.09.2020)
Published in Sleep (New York, N.Y.) (01.09.2020)
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Journal Article
Long-term effectiveness and safety of lemborexant in adults with insomnia disorder: results from a phase 3 randomized clinical trial
Yardley, Jane, Kärppä, Mikko, Inoue, Yuichi, Pinner, Kate, Perdomo, Carlos, Ishikawa, Kohei, Filippov, Gleb, Kubota, Naoki, Moline, Margaret
Published in Sleep medicine (01.04.2021)
Published in Sleep medicine (01.04.2021)
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Challenges and needs in cerebrovascular disease pathway: A qualitative descriptive study from the patients' and healthcare professionals' perspectives
Härkönen, Henna, Myllykangas, Kirsi, Gomes, Julius, Immonen, Milla, Kärppä, Mikko, Hyvämäki, Piia, Jansson, Miia
Published in Journal of advanced nursing (01.09.2024)
Published in Journal of advanced nursing (01.09.2024)
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Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population
Majamaa, Kari, Moilanen, Jukka S., Uimonen, Seija, Remes, Anne M., Salmela, Pasi I., Kärppä, Mikko, Majamaa-Voltti, Kirsi A.M., Rusanen, Harri, Sorri, Martti, Peuhkurinen, Keijo J., Hassinen, Ilmo E.
Published in American journal of human genetics (01.08.1998)
Published in American journal of human genetics (01.08.1998)
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Patient experiences on the quality of cerebrovascular diseases counselling using digital solutions in hospital—A qualitative research study
Myllykangas, Kirsi, Härkönen, Henna, Kääriäinen, Maria, Kärppä, Mikko, Jansson, Miia
Published in Journal of clinical nursing (01.06.2024)
Published in Journal of clinical nursing (01.06.2024)
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Journal Article
Phenotype of Patients With Charcot-Marie-Tooth With the p.His123Arg Mutation in GDAP1 in Northern Finland
Lehtilahti, Maria, Kallio, Mika, Majamaa, Kari, Kärppä, Mikko
Published in Neurology. Genetics (01.12.2021)
Published in Neurology. Genetics (01.12.2021)
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Journal Article
Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype
Kärppä, Mikko, Kytövuori, Laura, Saari, Markku, Majamaa, Kari
Published in BMC neurology (20.09.2018)
Published in BMC neurology (20.09.2018)
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Journal Article
Atypical phenotypes in titinopathies explained by second titin mutations
Evilä, Anni, Vihola, Anna, Sarparanta, Jaakko, Raheem, Olayinka, Palmio, Johanna, Sandell, Satu, Eymard, Bruno, Illa, Isabel, Rojas-Garcia, Ricard, Hankiewicz, Karolina, Negrão, Luis, Löppönen, Tuija, Nokelainen, Pekka, Kärppä, Mikko, Penttilä, Sini, Screen, Mark, Suominen, Tiina, Richard, Isabelle, Hackman, Peter, Udd, Bjarne
Published in Annals of neurology (01.02.2014)
Published in Annals of neurology (01.02.2014)
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Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family
Kullar, Peter J, Gomez-Duran, Aurora, Gammage, Payam A, Garone, Caterina, Minczuk, Michal, Golder, Zoe, Wilson, Janet, Montoya, Julio, Häkli, Sanna, Kärppä, Mikko, Horvath, Rita, Majamaa, Kari, Chinnery, Patrick F
Published in Brain (London, England : 1878) (01.01.2018)
Published in Brain (London, England : 1878) (01.01.2018)
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Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate‐induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy
Hynynen, Johanna, Pokka, Tytti, Komulainen‐Ebrahim, Jonna, Myllynen, Päivi, Kärppä, Mikko, Pylvänen, Laura, Kälviäinen, Reetta, Sokka, Arja, Jyrkilä, Aino, Lähdetie, Jaana, Haataja, Leena, Mäkitalo, Anna, Ylikotila, Pauli, Eriksson, Kai, Haapala, Piia, Ansakorpi, Hanna, Hinttala, Reetta, Vieira, Päivi, Majamaa, Kari, Rantala, Heikki, Uusimaa, Johanna
Published in Epilepsia (Copenhagen) (01.11.2018)
Published in Epilepsia (Copenhagen) (01.11.2018)
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Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small‐fiber and mixed neuropathy
Samuelsson, Kristin, Radovic, Ana, Press, Rayomand, Auranen, Mari, Ylikallio, Emil, Tyynismaa, Henna, KäRppä, Mikko, Veteläinen, Matilda, Peltola, Niina, Mellgren, Svein Ivar, Mygland, Åse, Tallaksen, Chantal, Andersen, Henning, Terkelsen, Astrid Juhl, Fontain, Freja, Hietaharju, Aki
Published in Muscle & nerve (01.03.2019)
Published in Muscle & nerve (01.03.2019)
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