Kalimo H - 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: kalimo h. Eur J Hum Genet. 2004 Oct;12(10):813-9. doi: 10.1038/sj.ejhg.5201221. Eur J Hum Genet. 2004. PMID: 15378071

2

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: kalimo h. Stroke. 2004 May;35(5):1063-7. doi: 10.1161/01.STR.0000124124.69842.2d. Epub 2004 Mar 11. Stroke. 2004. PMID: 15017012

3

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: kalimo h. 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.

4

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: kalimo h. Neurogenetics. 2006 Jul;7(3):185-94. doi: 10.1007/s10048-006-0049-x. Epub 2006 Jun 29. Neurogenetics. 2006. PMID: 16807713

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: kalimo h. Stroke. 2001 Aug;32(8):1767-74. doi: 10.1161/01.str.32.8.1767. Stroke. 2001. PMID: 11486103

6

Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy.

Vilkki J, Savontaus ML, Kalimo H, Nikoskelainen EK. Vilkki J, et al. Among authors: kalimo h. Hum Genet. 1989 Jun;82(3):208-12. doi: 10.1007/BF00291155. Hum Genet. 1989. PMID: 2567271

7

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.

Tikka S, Mykkänen K, Ruchoux MM, Bergholm R, Junna M, Pöyhönen M, Yki-Järvinen H, Joutel A, Viitanen M, Baumann M, Kalimo H. Tikka S, et al. Among authors: kalimo h. Brain. 2009 Apr;132(Pt 4):933-9. doi: 10.1093/brain/awn364. Epub 2009 Jan 27. Brain. 2009. PMID: 19174371 Free PMC article.

8

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: kalimo h. 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.

9

CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.

Kalimo H, Ruchoux MM, Viitanen M, Kalaria RN. Kalimo H, et al. Brain Pathol. 2002 Jul;12(3):371-84. doi: 10.1111/j.1750-3639.2002.tb00451.x. Brain Pathol. 2002. PMID: 12146805 Free PMC article. Review.

10

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: kalimo h. Stroke. 2004 Jul;35(7):1598-602. doi: 10.1161/01.STR.0000129787.92085.0a. Epub 2004 May 13. Stroke. 2004. PMID: 15143298

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