Transient increase in plasma brain (b‐type) natriuretic peptide after percutaneous transluminal coronary angioplasty von Tateishi, Jun, Masutani, Motomaru, Ohyanagi, Mitsumasa, Iwasaki, Tadaaki

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Typing prion isoforms von Parchi, P, Capellari, S, Chen, S. G, Petersen, R. B, Gambetti, P, Kopp, N, Brown, P, Kitamoto, T, Tateishi, J, Giese, A, Kretzschmar, H

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Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP von Ghetti, Bernardino, Piccardo, Pedro, Spillantini, Maria Grazia, Ichimiya, Yousuke, Porro, Monica, Perini, Francesco, Kitamoto, Tetsuyuki, Tateishi, Jun, Seiler, Charles, Frangione, Blas, Bugiani, Orso, Giaccone, Giorgio, Prelli, Frances, Goedert, Michel, Dlouhy, Stephen R., Tagliavini, Fabrizio

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An Amber Mutation of Prion Protein in Gerstmann-Sträussler Syndrome with Mutant PrP Plaques von Kitamoto, T., Iizuka, R., Tateishi, J.

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Prospective 10-year surveillance of human prion diseases in Japan von Nozaki, Ichiro, Hamaguchi, Tsuyoshi, Sanjo, Nobuo, Noguchi-Shinohara, Moeko, Sakai, Kenji, Nakamura, Yosikazu, Sato, Takeshi, Kitamoto, Tetsuyuki, Mizusawa, Hidehiro, Moriwaka, Fumio, Shiga, Yusei, Kuroiwa, Yoshiyuki, Nishizawa, Masatoyo, Kuzuhara, Shigeki, Inuzuka, Takashi, Takeda, Masatoshi, Kuroda, Shigetoshi, Abe, Koji, Murai, Hiroyuki, Murayama, Shigeo, Tateishi, Jun, Takumi, Ichiro, Shirabe, Susumu, Harada, Masafumi, Sadakane, Atsuko, Yamada, Masahito

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Novel Missense Variants of Prion Protein in Creutzfeldt-Jakob Disease or Gerstmann-Sträussler Syndrome von Kitamoto, T., Ohta, M., Dohura, K., Hitoshi, S., Terao, Y., Tateishi, J.

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Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease von Kitamoto, T, Muramoto, T, Mohri, S, Doh-Ura, K, Tateishi, J

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Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents von TATEISHI, J, KITAMOTO, T, HOQUE, M. Z, FURUKAWA, H

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Alpha B-crystallin and 27-kd heat shock protein are regulated by stress conditions in the central nervous system and accumulate in Rosenthal fibers von Iwaki, T, Iwaki, A, Tateishi, J, Sakaki, Y, Goldman, JE

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Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt- Jakob disease von Kitamoto, T, Shin, RW, Doh-ura, K, Tomokane, N, Miyazono, M, Muramoto, T, Tateishi, J

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Accumulation of alpha B-crystallin in central nervous system glia and neurons in pathologic conditions von Iwaki, T, Wisniewski, T, Iwaki, A, Corbin, E, Tomokane, N, Tateishi, J, Goldman, JE

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Sense and Antisense Modification of Glial αB-Crystallin Production Results in Alterations of Stress Fiber Formation and Thermoresistance von Iwaki, Toru, Iwaki, Akiko, Tateishi, Jun, Goldman, James E.

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Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease von Shibuya, S, Higuchi, J, Shin, R-W, Tateishi, J, Kitamoto, T

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CJD discrepancy von DOH-URA, K, KITAMOTO, T, SAKAKI, Y, TATEISHI, J

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Beta-protein amyloid is widely distributed in the central nervous system of patients with Alzheimer's disease von Ogomori, K, Kitamoto, T, Tateishi, J, Sato, Y, Suetsugu, M, Abe, M

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A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype von Majtényi, C, Brown, P, Cervenáková, L, Goldfarb, L G, Tateishi, J

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Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold von Tomokane, N, Iwaki, T, Tateishi, J, Iwaki, A, Goldman, JE

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Subacute myelo-optico-neuropathy: Clioquinol intoxication in humans and animals von Tateishi, Jun

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The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease von Muramoto, T, Kitamoto, T, Tateishi, J, Goto, I

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Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies von Kitamoto, T, Tateishi, J

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