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  1. Article

    Open Access

    Proteome Analysis of Cultivated Vascular Smooth Muscle Cells from a CADASIL Patient

    Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a vascular dementing disease caused by mutations in the NOTCH3 gene, most which are missense mutations leadi...

    Saara Ihalainen, Rabah Soliymani, Erika Iivanainen, Kati Mykkänen in Molecular Medicine (2007)

  2. Article

    Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL

    Johanna Annunen-Rasila, Saara Finnilä, Kati Mykkänen, Jukka S. Moilanen in Neurogenetics (2006)

  3. No Access

    Article

    Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL

    Mutations in the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), which is clinically characterised by recurrent ischemic strokes, migraine w...

    Johanna Annunen-Rasila, Saara Finnilä, Kati Mykkänen, Jukka S. Moilanen in Neurogenetics (2006)