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Stroke|April 18, 2009
Different clinical phenotypes in monozygotic CADASIL twins with a novel NOTCH3 mutationKati Mykkänen, Maija Junna, Kaarina Amberla, et al.Neurogenetics|June 30, 2006
Mitochondrial DNA sequence variation and mutation rate in patients with CADASILJohanna Annunen-Rasila, Saara Finnilä, Kati Mykkänen, et al.Molecular Medicine (Cambridge, Mass.)|July 12, 2007
Proteome analysis of cultivated vascular smooth muscle cells from a CADASIL patientSaara Ihalainen, Rabah Soliymani, Erika Iivanainen, et al.European Journal of Human Genetics : EJHG|September 21, 2004
Detection of the founder effect in Finnish CADASIL familiesKati Mykkänen, Marja-Liisa Savontaus, Vesa Juvonen, et al.Brain : a Journal of Neurology|January 29, 2009
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patientsSaara Tikka, Kati Mykkänen, Marie-Magdeleine Ruchoux, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 6, 2012
CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cellsSaara Tikka, Yan Peng Ng, Giuseppe Di Maio, et al.RMD Open|January 3, 2025
Reliability of the OMERACT Giant cell arteritis Ultrasonography Score (OGUS): results of a patient-based exercise involving experts and non-experts in vascular ultrasonographyChristina Duftner, Norbert Redlinger, George A Bruyn, et al.Pageof 1