Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease.

Por Kitamoto, T, Muramoto, T, Mohri, S, Doh-Ura, K, Tateishi, J
Publicado em 1991

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system.

Por Kitamoto, T., Doh-ura, K., Muramoto, T., Miyazono, M., Tateishi, J.
Publicado em 1992

A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation.

Por Miyazono, M., Iwaki, T., Kitamoto, T., Kaneko, Y., Doh-ura, K., Tateishi, J.
Publicado em 1991

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.

Por Kitamoto, T., Shin, R. W., Doh-ura, K., Tomokane, N., Miyazono, M., Muramoto, T., Tateishi, J.
Publicado em 1992

Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.

Por Tranchant, C, Doh-ura, K, Warter, J M, Steinmetz, G, Chevalier, Y, Hanauer, A, Kitamoto, T, Tateishi, J
Publicado em 1992

Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

Por TANIWAKI, Y, HARA, H, DOH-URA, K, MURAKAMI, I, TASHIRO, H, YAMASAKI, T, SHIGETO, H, ARAKAWA, K, ARAKI, E, YAMADA, T, IWAKI, T, KIRA, J
Publicado em 2000