Authors: Finnila, S Tuisku, S Herva, R Majamaa, K

Citation: S. Finnila et al., A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL, J MOL MED-J, 79(11), 2001, pp. 641-647

Authors: Bode, MK Tikkakoski, T Tuisku, S Kronqvist, E Tuominen, H

Citation: Mk. Bode et al., Isolated neurosarcoidosis - MR findings and pathologic correlation - A case report, ACT RADIOL, 42(6), 2001, pp. 563-567

Authors: Tuominen, S Juvonen, V Amberla, K Jolma, T Rinne, JO Tuisku, S Kurki, T Marttila, R Poyhonen, M Savontaus, ML Viitanen, M Kalimo, H

Citation: S. Tuominen et al., Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation, STROKE, 32(8), 2001, pp. 1767-1774

Authors: Kalimo, H Viitanen, M Amberla, K Juvonen, V Marttila, R Poyhonen, M Rinne, JO Savontaus, ML Tuisku, S Winblad, B

Citation: H. Kalimo et al., CADASIL: hereditary disease of arteries causing brain infarcts and dementia, NEUROP AP N, 25(4), 1999, pp. 257-265