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Neuropathology and Applied Neurobiology|October 24, 2009
Brain pathology in three subjects from the same pedigree with presenilin-1 (PSEN1) P264L mutationP Martikainen, M Pikkarainen, K Pöntynen, et al.Journal of Refractive Surgery (Thorofare, N.J. : 1995)|September 25, 2008
Photorefractive keratectomy retreatment after LASIKWaldir Neira-Zalentein, Jukka A O Moilanen, Ilpo S Tuisku, et al.Neuropathology and Applied Neurobiology|September 4, 1999
CADASIL: hereditary disease of arteries causing brain infarcts and dementiaH Kalimo, M Viitanen, K Amberla, et al.Acta Ophthalmologica|June 8, 2023
Epithelial recurrent erosion dystrophy (ERED) from the splice site altering COL17A1 variant c.3156C>T in families of Finnish-Swedish ancestryJoni A Turunen, Ilpo S Tuisku, Pauliina Repo, et al.Stroke|August 4, 2001
Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutationS Tuominen, V Juvonen, K Amberla, et al.Pageof 2