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

Year Number of Results
1961 1
1994 1
1995 1
2001 2
2002 2
2003 2
2004 1
2005 2
2006 3
2007 3
2008 7
2009 8
2010 12
2011 16
2012 13
2013 5
2014 4
2015 6
2016 5
2017 4
2018 4
2019 2
2020 5
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Similar Articles for PMID: 22268086

93 results
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Sensorimotor, visual, and auditory cortical atrophy in Unverricht-Lundborg disease mapped with cortical thickness analysis.
Koskenkorva P, Niskanen E, Hyppönen J, Könönen M, Mervaala E, Soininen H, Kälviäinen R, Vanninen R. Koskenkorva P, et al. AJNR Am J Neuroradiol. 2012 May;33(5):878-83. doi: 10.3174/ajnr.A2882. Epub 2012 Jan 19. AJNR Am J Neuroradiol. 2012. PMID: 22268086 Free article.
Motor cortex and thalamic atrophy in Unverricht-Lundborg disease: voxel-based morphometric study.
Koskenkorva P, Khyuppenen J, Niskanen E, Könönen M, Bendel P, Mervaala E, Lehesjoki AE, Kälviäinen R, Vanninen R. Koskenkorva P, et al. Neurology. 2009 Aug 25;73(8):606-11. doi: 10.1212/WNL.0b013e3181b3888b. Neurology. 2009. PMID: 19704079
Altered cortical inhibition in Unverricht-Lundborg type progressive myoclonus epilepsy (EPM1).
Danner N, Julkunen P, Khyuppenen J, Hukkanen T, Könönen M, Säisänen L, Koskenkorva P, Vanninen R, Lehesjoki AE, Kälviäinen R, Mervaala E. Danner N, et al. Epilepsy Res. 2009 Jul;85(1):81-8. doi: 10.1016/j.eplepsyres.2009.02.015. Epub 2009 Mar 24. Epilepsy Res. 2009. PMID: 19321308
Reduced cortical activation in inferior frontal junction in Unverricht-Lundborg disease (EPM1) - A motor fMRI study.
Könönen M, Danner N, Koskenkorva P, Kälviäinen R, Hyppönen J, Mervaala E, Karjalainen P, Vanninen R, Niskanen E. Könönen M, et al. Epilepsy Res. 2015 Mar;111:78-84. doi: 10.1016/j.eplepsyres.2015.01.006. Epub 2015 Jan 24. Epilepsy Res. 2015. PMID: 25769376
Severer phenotype in Unverricht-Lundborg disease (EPM1) patients compound heterozygous for the dodecamer repeat expansion and the c.202C>T mutation in the CSTB gene.
Koskenkorva P, Hyppönen J, Aikiä M, Mervaala E, Kiviranta T, Eriksson K, Lehesjoki AE, Vanninen R, Kälviäinen R. Koskenkorva P, et al. Neurodegener Dis. 2011;8(6):515-22. doi: 10.1159/000323470. Epub 2011 Jul 15. Neurodegener Dis. 2011. PMID: 21757863
Thickened skull, scoliosis and other skeletal findings in Unverricht-Lundborg disease link cystatin B function to bone metabolism.
Suoranta S, Manninen H, Koskenkorva P, Könönen M, Laitinen R, Lehesjoki AE, Kälviäinen R, Vanninen R. Suoranta S, et al. Bone. 2012 Dec;51(6):1016-24. doi: 10.1016/j.bone.2012.08.123. Epub 2012 Aug 23. Bone. 2012. PMID: 23010349
White matter degeneration with Unverricht-Lundborg progressive myoclonus epilepsy: a translational diffusion-tensor imaging study in patients and cystatin B-deficient mice.
Manninen O, Koskenkorva P, Lehtimäki KK, Hyppönen J, Könönen M, Laitinen T, Kalimo H, Kopra O, Kälviäinen R, Gröhn O, Lehesjoki AE, Vanninen R. Manninen O, et al. Radiology. 2013 Oct;269(1):232-9. doi: 10.1148/radiol.13122458. Epub 2013 Jun 20. Radiology. 2013. PMID: 23788720
Alterations of motor cortical excitability and anatomy in Unverricht-Lundborg disease.
Danner N, Julkunen P, Hyppönen J, Niskanen E, Säisänen L, Könönen M, Koskenkorva P, Vanninen R, Kälviäinen R, Mervaala E. Danner N, et al. Mov Disord. 2013 Nov;28(13):1860-7. doi: 10.1002/mds.25615. Epub 2013 Aug 7. Mov Disord. 2013. PMID: 23925991
TMS-EEG reveals impaired intracortical interactions and coherence in Unverricht-Lundborg type progressive myoclonus epilepsy (EPM1).
Julkunen P, Säisänen L, Könönen M, Vanninen R, Kälviäinen R, Mervaala E. Julkunen P, et al. Epilepsy Res. 2013 Sep;106(1-2):103-12. doi: 10.1016/j.eplepsyres.2013.04.001. Epub 2013 Apr 30. Epilepsy Res. 2013. PMID: 23642573
Refining the phenotype of Unverricht-Lundborg disease (EPM1): a population-wide Finnish study.
Hyppönen J, Äikiä M, Joensuu T, Julkunen P, Danner N, Koskenkorva P, Vanninen R, Lehesjoki AE, Mervaala E, Kälviäinen R. Hyppönen J, et al. Neurology. 2015 Apr 14;84(15):1529-36. doi: 10.1212/WNL.0000000000001466. Epub 2015 Mar 13. Neurology. 2015. PMID: 25770194
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