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Journal of the Neurological Sciences|September 15, 1996
A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210H Furukawa, T Kitamoto, H Hashiguchi, et al.Brain Research|January 29, 1990
Cerebral amyloid in mice with Creutzfeldt-Jakob disease is influenced by the strain of the infectious agentT Kitamoto, R Yi, S Mohri, et al.Clinical Neuropathology|November 1, 1996
Immunhistological evaluation of Creutzfeldt-Jakob disease with reference to the type PrPres depositionJ Tateishi, T Kitamoto, H Kretzschmar, et al.Brain Research. Molecular Brain Research|June 1, 1995
New variant prion protein in a Japanese family with Gerstmann-Sträussler syndromeH Furukawa, T Kitamoto, Y Tanaka, et al.Brain Research|December 3, 1986
Congophilia in cerebral amyloidosis is modified by inactivation procedures on slow transmissible pathogensT Tashima, T Kitamoto, J Tateishi, et al.Acta Neuropathologica|January 1, 1992
The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long durationT Muramoto, T Kitamoto, H Koga, et al.Acta Neuropathologica|January 1, 1989
Ferritin immunohistochemistry as a marker for microgliaY Kaneko, T Kitamoto, J Tateishi, et al.Acta Neuropathologica|January 1, 1992
Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndromeM Miyazono, T Kitamoto, T Iwaki, 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.The American Journal of Pathology|June 1, 1989
Increased tau accumulation in senile plaques as a hallmark in Alzheimer's diseaseR W Shin, K Ogomori, T Kitamoto, et al.Pageof 28