Päivärinta M - Search Results

1

Epidemiology of Huntington's disease in Finland.

Sipilä JO, Hietala M, Siitonen A, Päivärinta M, Majamaa K. Sipilä JO, et al. Among authors: paivarinta m. Parkinsonism Relat Disord. 2015 Jan;21(1):46-9. doi: 10.1016/j.parkreldis.2014.10.025. Epub 2014 Nov 3. Parkinsonism Relat Disord. 2015. PMID: 25466405 Free article.

2

Why We Still Need More Research on the Epidemiology of Huntington's Disease.

Sipilä JO, Päivärinta M. Sipilä JO, et al. Among authors: paivarinta m. Neuroepidemiology. 2016;46(2):154-5. doi: 10.1159/000444230. Epub 2016 Feb 3. Neuroepidemiology. 2016. PMID: 26836497 Free article. No abstract available.

3

Comparison of mid-age-onset and late-onset Huntington's disease in Finnish patients.

Sipilä JOT, Kauko T, Päivärinta M, Majamaa K. Sipilä JOT, et al. Among authors: paivarinta m. J Neurol. 2017 Oct;264(10):2095-2100. doi: 10.1007/s00415-017-8600-2. Epub 2017 Aug 28. J Neurol. 2017. PMID: 28849405 Free article.

4

Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion.

Juvonen V, Hietala M, Päivärinta M, Rantamäki M, Hakamies L, Kaakkola S, Vierimaa O, Penttinen M, Savontaus ML. Juvonen V, et al. Among authors: paivarinta m. Ann Neurol. 2000 Sep;48(3):354-61. Ann Neurol. 2000. PMID: 10976642

5

Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutation.

Martikainen MH, Päivärinta M, Hietala M, Kaasinen V. Martikainen MH, et al. Among authors: paivarinta m. Neurol Genet. 2015 Oct 15;1(4):e27. doi: 10.1212/NXG.0000000000000027. eCollection 2015 Dec. Neurol Genet. 2015. PMID: 27066564 Free PMC article.

6

SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population.

Pasanen P, Palin E, Pohjolan-Pirhonen R, Pöyhönen M, Rinne JO, Päivärinta M, Martikainen MH, Kaasinen V, Hietala M, Gardberg M, Saukkonen AM, Eerola-Rautio J, Kaakkola S, Lyytinen J, Tienari PJ, Paetau A, Suomalainen A, Myllykangas L. Pasanen P, et al. Among authors: paivarinta m. Neurobiol Aging. 2017 Feb;50:168.e5-168.e8. doi: 10.1016/j.neurobiolaging.2016.10.014. Epub 2016 Oct 19. Neurobiol Aging. 2017. PMID: 27838048

7

Steroid-responsive encephalopathy with a peculiar CSF biomarker profile in an 89-year-old man.

Sipilä JOT, Rissanen E, Korpela J, Päivärinta M. Sipilä JOT, et al. Among authors: paivarinta m. Oxf Med Case Reports. 2018 Sep 24;2018(10):omy073. doi: 10.1093/omcr/omy073. eCollection 2018 Oct. Oxf Med Case Reports. 2018. PMID: 30263128 Free PMC article.

8

Successful treatment of POLG-related mitochondrial epilepsy with antiepileptic drugs and low glycaemic index diet.

Martikainen MH, Päivärinta M, Jääskeläinen S, Majamaa K. Martikainen MH, et al. Among authors: paivarinta m. Epileptic Disord. 2012 Dec;14(4):438-41. doi: 10.1684/epd.2012.0543. Epileptic Disord. 2012. PMID: 23248042 Free article.

9

Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus.

Uusimaa J, Hinttala R, Rantala H, Päivärinta M, Herva R, Röyttä M, Soini H, Moilanen JS, Remes AM, Hassinen IE, Majamaa K. Uusimaa J, et al. Among authors: paivarinta m. Epilepsia. 2008 Jun;49(6):1038-45. doi: 10.1111/j.1528-1167.2008.01544.x. Epub 2008 Feb 20. Epilepsia. 2008. PMID: 18294203 Free article.

10

Discrepancies in reporting the CAG repeat lengths for Huntington's disease.

Quarrell OW, Handley O, O'Donovan K, Dumoulin C, Ramos-Arroyo M, Biunno I, Bauer P, Kline M, Landwehrmeyer GB; European Huntington’s Disease Network. Quarrell OW, et al. Eur J Hum Genet. 2012 Jan;20(1):20-6. doi: 10.1038/ejhg.2011.136. Epub 2011 Aug 3. Eur J Hum Genet. 2012. PMID: 21811303 Free PMC article.

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