Pöyhönen M - Search Results

1

CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cells.

Tikka S, Ng YP, Di Maio G, Mykkänen K, Siitonen M, Lepikhova T, Pöyhönen M, Viitanen M, Virtanen I, Kalimo H, Baumann M. Tikka S, et al. Among authors: poyhonen m. J Cereb Blood Flow Metab. 2012 Dec;32(12):2171-80. doi: 10.1038/jcbfm.2012.123. Epub 2012 Sep 5. J Cereb Blood Flow Metab. 2012. PMID: 22948298 Free PMC article. Clinical Trial.

2

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

3

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.

4

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

5

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

6

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

7

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

8

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

9

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.

10

Neurologic symptoms are common during gestation and puerperium in CADASIL.

Roine S, Pöyhönen M, Timonen S, Tuisku S, Marttila R, Sulkava R, Kalimo H, Viitanen M. Roine S, et al. Among authors: poyhonen m. Neurology. 2005 Apr 26;64(8):1441-3. doi: 10.1212/01.WNL.0000158655.71323.8A. Neurology. 2005. PMID: 15851739

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