Showing results (1-10 of 636) with videos related to
Sort By:
Pageof 64
Journal of the Neurological Sciences|July 17, 1998
A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob diseaseH Furukawa, K Doh-ura, H Kikuchi, et al.Rinsho Shinkeigaku = Clinical Neurology|December 1, 1996
[Prion diseases and a new variant of Creutzfeldt-Jakob disease]K Doh-ura, T KitamotoJournal of Virology|April 25, 2000
Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulationK Doh-Ura, T Iwaki, B CaugheyPathology International|July 27, 1999
Argyrophilic grains in late-onset Creutzfeldt-Jakob diseased brainT Kawashima, K Doh-ura, T IwakiRinsho Shinkeigaku = Clinical Neurology|February 1, 1989
[Recurrent unilateral painful oculomotor nerve palsy with an ipsilateral posterior ethmoidal mucocele]K Doh-ura, J Kira, Y Itoyama, et al.Microbial Pathogenesis|January 1, 1995
Identification of differentially expressed genes in scrapie-infected mouse neuroblastoma cellsK Doh-ura, S Perryman, R Race, et al.Neurology|February 1, 1991
A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Sträussler syndromeT Kitamoto, K Yamaguchi, K Doh-ura, et al.Acta Neuropathologica|June 23, 1999
Preferential neurodegeneration in the cervical spinal cord of progressive supranuclear palsyH Kikuchi, K Doh-ura, J Kira, et al.Acta Neuropathologica|November 9, 2001
Cognitive dysfunction in patients with amyotrophic lateral sclerosis is associated with spherical or crescent-shaped ubiquitinated intraneuronal inclusions in the parahippocampal gyrus and amygdala, but not in the neostriatumT Kawashima, K Doh-ura, H Kikuchi, et al.Journal of Neuropathology and Experimental Neurology|September 27, 2000
Enhanced CD9 expression in the mouse and human brains infected with transmissible spongiform encephalopathiesK Doh-ura, E Mekada, K Ogomori, et al.Pageof 64