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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 2
2004 1
2005 1
2006 2
2007 2
2009 2
2010 2
2012 1
2013 1
2014 2
2015 1
2016 2
2017 3
2018 4
2019 1
2020 1
2021 5
2023 1
2024 2

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32 results

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Page 1
Feasibility and patient acceptability of a commercially available wearable and a smart phone application in identification of motor states in parkinson's disease.
Liikkanen S, Sinkkonen J, Suorsa J, Kaasinen V, Pekkonen E, Kärppä M, Scheperjans F, Huttunen T, Sarapohja T, Pesonen U, Kuoppamäki M, Keränen T. Liikkanen S, et al. Among authors: karppa m. PLOS Digit Health. 2023 Apr 7;2(4):e0000225. doi: 10.1371/journal.pdig.0000225. eCollection 2023 Apr. PLOS Digit Health. 2023. PMID: 37027348 Free PMC article.
Hartia-lantiodystrofioiden molekyyligenetiikka Suomessa.
Raheem O, Suominen T, Hackman P, Vihola A, Auranen M, Kalimo H, Mahjneh I, Kärppä M, Haapasalo H, Udd B. Raheem O, et al. Among authors: karppa m. Duodecim. 2006;122(17):2130-6. Duodecim. 2006. PMID: 17115630 Finnish. No abstract available.
Validation of the Finnish Version of the Unified Dyskinesia Rating Scale.
Kaasinen V, Scheperjans F, Kärppä M, Korpela J, Brück A, Sipilä JOT, Joutsa J, Järvelä J, Eerola-Rautio J, Martikainen MH, Airaksinen K, Stebbins GT, Martinez-Martin P, Goetz CG, Lin J, Luo S, Pekkonen E. Kaasinen V, et al. Among authors: karppa m. Eur Neurol. 2021;84(6):444-449. doi: 10.1159/000517369. Epub 2021 Jul 14. Eur Neurol. 2021. PMID: 34261060
Amyloid myopathy: a diagnostic challenge.
Tuomaala H, Kärppä M, Tuominen H, Remes AM. Tuomaala H, et al. Among authors: karppa m. Neurol Int. 2009 Nov 16;1(1):e7. doi: 10.4081/ni.2009.e7. Neurol Int. 2009. PMID: 21577365 Free PMC article.
Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy.
Samuelsson K, Radovic A, Press R, Auranen M, Ylikallio E, Tyynismaa H, KäRppä M, Veteläinen M, Peltola N, Mellgren SI, Mygland Å, Tallaksen C, Andersen H, Terkelsen AJ, Fontain F, Hietaharju A. Samuelsson K, et al. Among authors: karppa m. Muscle Nerve. 2019 Mar;59(3):354-357. doi: 10.1002/mus.26348. Epub 2018 Dec 4. Muscle Nerve. 2019. PMID: 30246259
Atypical phenotypes in titinopathies explained by second titin mutations.
Evilä A, Vihola A, Sarparanta J, Raheem O, Palmio J, Sandell S, Eymard B, Illa I, Rojas-Garcia R, Hankiewicz K, Negrão L, Löppönen T, Nokelainen P, Kärppä M, Penttilä S, Screen M, Suominen T, Richard I, Hackman P, Udd B. Evilä A, et al. Among authors: karppa m. Ann Neurol. 2014 Feb;75(2):230-40. doi: 10.1002/ana.24102. Epub 2014 Feb 24. Ann Neurol. 2014. PMID: 24395473
Hereditary myopathy with early respiratory failure: occurrence in various populations.
Palmio J, Evilä A, Chapon F, Tasca G, Xiang F, Brådvik B, Eymard B, Echaniz-Laguna A, Laporte J, Kärppä M, Mahjneh I, Quinlivan R, Laforêt P, Damian M, Berardo A, Taratuto AL, Bueri JA, Tommiska J, Raivio T, Tuerk M, Gölitz P, Chevessier F, Sewry C, Norwood F, Hedberg C, Schröder R, Edström L, Oldfors A, Hackman P, Udd B. Palmio J, et al. Among authors: karppa m. J Neurol Neurosurg Psychiatry. 2014 Mar;85(3):345-53. doi: 10.1136/jnnp-2013-304965. Epub 2013 Apr 19. J Neurol Neurosurg Psychiatry. 2014. PMID: 23606733
32 results