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Year Number of Results
1990 1
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1993 4
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1997 3
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1999 2
2000 8
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2002 1
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2004 8
2005 3
2006 3
2007 3
2009 3
2010 1
2011 2
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2013 3
2014 6
2015 3
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107 results

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Page 1
CADASIL and CARASIL.
Tikka S, Baumann M, Siitonen M, Pasanen P, Pöyhönen M, Myllykangas L, Viitanen M, Fukutake T, Cognat E, Joutel A, Kalimo H. Tikka S, et al. Among authors: poyhonen m. Brain Pathol. 2014 Sep;24(5):525-44. doi: 10.1111/bpa.12181. Brain Pathol. 2014. PMID: 25323668 Free PMC article. Review.
Genetics of dementia in a Finnish cohort.
Pasanen P, Myllykangas L, Pöyhönen M, Kiviharju A, Siitonen M, Hardy J, Bras J, Paetau A, Tienari PJ, Guerreiro R, Verkkoniemi-Ahola A. Pasanen P, et al. Among authors: poyhonen m. Eur J Hum Genet. 2018 Jun;26(6):827-837. doi: 10.1038/s41431-018-0117-3. Epub 2018 Feb 23. Eur J Hum Genet. 2018. PMID: 29476165 Free PMC article.
Genetic analysis reveals novel variants for vascular cognitive impairment.
Mönkäre S, Kuuluvainen L, Schleutker J, Bras J, Roine S, Pöyhönen M, Guerreiro R, Myllykangas L. Mönkäre S, et al. Among authors: poyhonen m. Acta Neurol Scand. 2022 Jul;146(1):42-50. doi: 10.1111/ane.13613. Epub 2022 Mar 20. Acta Neurol Scand. 2022. PMID: 35307828 Free PMC article.
Whole-exome sequencing of Finnish patients with vascular cognitive impairment.
Mönkäre S, Kuuluvainen L, Kun-Rodrigues C, Carmona S, Schleutker J, Bras J, Pöyhönen M, Guerreiro R, Myllykangas L. Mönkäre S, et al. Among authors: poyhonen m. Eur J Hum Genet. 2021 Apr;29(4):663-671. doi: 10.1038/s41431-020-00775-9. Epub 2020 Dec 2. Eur J Hum Genet. 2021. PMID: 33268848 Free PMC article.
CADASIL: hereditary disease of arteries causing brain infarcts and dementia.
Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, Pöyhönen M, Rinne JO, Savontaus M, Tuisku S, Winblad B. Kalimo H, et al. Among authors: poyhonen m. Neuropathol Appl Neurobiol. 1999 Aug;25(4):257-65. doi: 10.1046/j.1365-2990.1999.00198.x. Neuropathol Appl Neurobiol. 1999. PMID: 10476042 Review.
107 results