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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: viitanen m. Eur J Hum Genet. 2004 Oct;12(10):813-9. doi: 10.1038/sj.ejhg.5201221. Eur J Hum Genet. 2004. PMID: 15378071
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
Annunen-Rasila J, Finnilä S, Mykkänen K, Moilanen JS, Veijola J, Pöyhönen M, Viitanen M, Kalimo H, Majamaa K. Annunen-Rasila J, et al. Among authors: viitanen m. Neurogenetics. 2006 Jul;7(3):185-94. doi: 10.1007/s10048-006-0049-x. Epub 2006 Jun 29. Neurogenetics. 2006. PMID: 16807713
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: viitanen m. Stroke. 2004 Jul;35(7):1598-602. doi: 10.1161/01.STR.0000129787.92085.0a. Epub 2004 May 13. Stroke. 2004. PMID: 15143298
Arterioles of the lenticular nucleus in CADASIL.
Miao Q, Paloneva T, Tuisku S, Roine S, Poyhonen M, Viitanen M, Kalimo H. Miao Q, et al. Among authors: viitanen m. Stroke. 2006 Sep;37(9):2242-7. doi: 10.1161/01.STR.0000236838.84150.c2. Epub 2006 Jul 27. Stroke. 2006. PMID: 16873707
324 results