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Clinical Molecular Pathology|June 1, 1996
Differential expression of CD44 variants among meningioma subtypesS O Suzuki, T Iwaki, T Kitamoto, et al.
Acta Neuropathologica|January 1, 1991
Increased senile plaques without microglia in Alzheimer's diseaseT Ohgami, T Kitamoto, R W Shin, et al.
The American Journal of Pathology|September 1, 1991
A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formationM Miyazono, T Iwaki, T Kitamoto, et al.
Biochemical and Biophysical Research Communications|March 15, 1993
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndromeT Kitamoto, M Ohta, K Doh-ura, et al.
Neurology|February 1, 1994
Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein geneI Inoue, T Kitamoto, K Doh-ura, et al.
Neuropathology and Applied Neurobiology|February 1, 1990
Immunogold light and electron microscopic detection of amyloid plaques in transmissible spongiform encephalopathiesJ Doerr-Schott, T Kitamoto, J Tateishi, et al.
Annals of Neurology|December 1, 1993
A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesisT Kitamoto, N Amano, Y Terao, et al.
Biologicals : Journal of the International Association of Biological Standardization|August 3, 2001
Scrapie removal using Planova virus removal filtersJ Tateishi, T Kitamoto, S Mohri, et al.
Neuroradiology|October 1, 1995
Serial MRI in early Creutzfeldt-Jacob disease with a point mutation of prion protein at codon 180S Ishida, M Sugino, N Koizumi, et al.
The American Journal of Pathology|June 1, 1992
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob diseaseT Kitamoto, R W Shin, K Doh-ura, et al.
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