Pöyhönen M - Search Results

1

Detection of the founder effect in Finnish CADASIL families.

Mykkänen K, Savontaus ML, Juvonen V, Sistonen P, Tuisku S, Tuominen S, Penttinen M, Lundkvist J, Viitanen M, Kalimo H, Pöyhönen M. Mykkänen K, et al. Among authors: poyhonen m. Eur J Hum Genet. 2004 Oct;12(10):813-9. doi: 10.1038/sj.ejhg.5201221. Eur J Hum Genet. 2004. PMID: 15378071

2

Tumor-independent Detection of Inherited Mismatch Repair Deficiency for the Diagnosis of Lynch Syndrome with High Specificity and Sensitivity.

Kansikas M, Vähätalo L, Kantelinen J, Kasela M, Putula J, Døhlen A, Paloviita P, Kärkkäinen E, Lahti N, Arnez P, Kilpinen S, Alcala-Repo B, Pylvänäinen K, Pöyhönen M, Peltomäki P, Järvinen HJ, Seppälä TT, Renkonen-Sinisalo L, Lepistö A, Mecklin JP, Nyström M. Kansikas M, et al. Among authors: poyhonen m. Cancer Res Commun. 2023 Mar 2;3(3):361-370. doi: 10.1158/2767-9764.CRC-22-0384. eCollection 2023 Mar. Cancer Res Commun. 2023. PMID: 36875157 Free PMC article.

3

Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description.

Haltia M, Viitanen M, Sulkava R, Ala-Hurula V, Poyhonen M, Goldfarb L, Brown P, Levy E, Houlden H, Crook R, et al. Haltia M, et al. Among authors: poyhonen m. Ann Neurol. 1994 Sep;36(3):362-7. doi: 10.1002/ana.410360307. Ann Neurol. 1994. PMID: 8080244

4

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.

5

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation.

Tuominen S, Juvonen V, Amberla K, Jolma T, Rinne JO, Tuisku S, Kurki T, Marttila R, Pöyhönen M, Savontaus ML, Viitanen M, Kalimo H. Tuominen S, et al. Among authors: poyhonen m. Stroke. 2001 Aug;32(8):1767-74. doi: 10.1161/01.str.32.8.1767. Stroke. 2001. PMID: 11486103

6

[CADASIL disease: a hereditary arterial disease leading to brain infarctions and dementia].

Kalimo H, Aho T, Amberla K, Baumann M, Herva R, Juvonen V, Kalimo K, Mononen H, Myllylä V, Pöyhönen M, Rinne J, Savontaus ML, Sonninen P, Sonninen V, Tuisku S, Viitanen M. Kalimo H, et al. Among authors: poyhonen m. Duodecim. 1998;114(20):2041-51. Duodecim. 1998. PMID: 11717724 Review. Finnish. No abstract available.

7

Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patients.

Tuominen S, Miao Q, Kurki T, Tuisku S, Pöyhönen M, Kalimo H, Viitanen M, Sipilä HT, Bergman J, Rinne JO. Tuominen S, et al. Among authors: poyhonen m. Stroke. 2004 May;35(5):1063-7. doi: 10.1161/01.STR.0000124124.69842.2d. Epub 2004 Mar 11. Stroke. 2004. PMID: 15017012

8

Insidious cognitive decline in CADASIL.

Amberla K, Wäljas M, Tuominen S, Almkvist O, Pöyhönen M, Tuisku S, Kalimo H, Viitanen M. Amberla K, et al. Among authors: poyhonen m. Stroke. 2004 Jul;35(7):1598-602. doi: 10.1161/01.STR.0000129787.92085.0a. Epub 2004 May 13. Stroke. 2004. PMID: 15143298

9

Scanning laser Doppler flowmetry shows reduced retinal capillary blood flow in CADASIL.

Harju M, Tuominen S, Summanen P, Viitanen M, Pöyhönen M, Nikoskelainen E, Kalimo H, Kivelä T. Harju M, et al. Among authors: poyhonen m. Stroke. 2004 Nov;35(11):2449-52. doi: 10.1161/01.STR.0000145048.94499.b9. Epub 2004 Oct 7. Stroke. 2004. PMID: 15472092

10

Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Miao Q, Paloneva T, Tuominen S, Pöyhönen M, Tuisku S, Viitanen M, Kalimo H. Miao Q, et al. Among authors: poyhonen m. Brain Pathol. 2004 Oct;14(4):358-64. doi: 10.1111/j.1750-3639.2004.tb00078.x. Brain Pathol. 2004. PMID: 15605982 Free PMC article.

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