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The American Journal of Pathology|December 1, 1991
Alzheimer's amyloid precursor protein-positive degenerative neurites exist even within kuru plaques not specific to Alzheimer's diseaseT Ohgami, T Kitamoto, A Weidmann, et al.Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1988
Incidence and characterization of age related amyloid deposits in the human anterior pituitary glandT Tashima, T Kitamoto, J Tateishi, et al.Biochemical and Biophysical Research Communications|September 15, 1989
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndromeK Doh-ura, J Tateishi, H Sasaki, et al.Journal of Virology|November 1, 1991
Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob diseaseT Kitamoto, T Muramoto, S Mohri, et al.Acta Neuropathologica|January 1, 1988
Focal intracerebral accumulation of a novel type of amyloid protein. An early stage of cerebral amyloidoma?A Hori, T Kitamoto, J Tateishi, et al.Acta Neuropathologica|January 1, 1992
Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutationsM Miyazono, T Kitamoto, K Doh-ura, et al.Annals of Neurology|June 18, 1998
Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob diseaseS Shibuya, J Higuchi, R W Shin, et al.The American Journal of Pathology|April 1, 1992
Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving methodR W Shin, T Iwaki, T Kitamoto, et al.Acta Neuropathologica|November 1, 1996
Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission studyM Z Hoque, T Kitamoto, H Furukawa, et al.Journal of Virology|November 1, 1993
Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob diseaseT Muramoto, T Kitamoto, M Z Hoque, et al.Pageof 28