Involvement of the nigrostriatal system in Gerstman–Sträussler–Scheinker disease with the PRNP-P102L mutation

Authors: Ono, Natsuki, Suzuyama, Kohei, Minagawa, Hiromu, Uwatoko, Kiku, Yoshikawa, Masaaki, Ide, Toshihiro, Mitsuoka, Miyuki, Honda, Kazuo, Hirai, Tetsuyoshi, Otsuka, Takateru, Kai, Keita, Honda, Hiroyuki, Kitamoto, Tetsuyuki, Irie, Hiroyuki, Yukitake, Motohiro, Koike, Haruki

Source: In Journal of the Neurological Sciences 15 September 2024 464

Vacuoles related to tissue neuron-astrocyte ratio and infiltration of macrophages/monocytes contribute to hyperintense brain signals on diffusion-weighted magnetic resonance imaging in sporadic Creutzfeldt-Jakob disease

Authors: Shima, Ayano, Sakai, Kenji, Yamashita, Fumio, Hamaguchi, Tsuyoshi, Kitamoto, Tetsuyuki, Sasaki, Makoto, Yamada, Masahito, Ono, Kenjiro

Source: In Journal of the Neurological Sciences 15 April 2023 447

Preventive or promotive effects of PRNP polymorphic heterozygosity on the onset of prion disease

Authors: Kai, Hideaki ^a, Teruya, Kenta ^b, Takeuchi, Atsuko ^a, Nakamura, Yoshikazu ^c, Mizusawa, Hidehiro ^d, Yamada, Masahito ^e, Kitamoto, Tetsuyuki ^{a, ∗}

Source: In Heliyon March 2023 9(3)

Propagation of Diffusion-Weighted MRI Abnormalities in the Preclinical Stage of Sporadic Creutzfeldt-Jakob Disease

Authors: Yasuda, Manato, Sugiyama, Atsuhiko, Hokkoku, Hideharu, Suichi, Tomoki, Ito, Kimiko, Satoh, Katsuya, Kitamoto, Tetsuyuki, Kuwabara, Satoshi

Source: Neurology. 99(16):699-702

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100180446186.0x000001&indx=1&recIds=ETOCvdc_100180446186.0x000001

An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings

Authors: Matsuo, Koushun, Goto, Daiki, Hasegawa, Masato, Ogita, Kenji, Koyama, Takeo, Akagi, Akio, Kitamoto, Tetsuyuki, Yoshida, Mari, Iwasaki, Yasushi

Source: Neuropathology. 42(3):245-253

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100151884291.0x000001&indx=1&recIds=ETOCvdc_100151884291.0x000001

Specific electroencephalogram features in the very early phases of sporadic Creutzfeldt–Jakob disease

Authors: Matsubayashi, Taiki, Akaza, Miho, Hayashi, Yuichi, Hamaguchi, Tsuyoshi, Satoh, Katsuya, Kosami, Koki, Ae, Ryusuke, Kitamoto, Tetsuyuki, Yamada, Masahito, Shimohata, Takayoshi, Yokota, Takanori, Sanjo, Nobuo

Source: In Journal of the Neurological Sciences 15 June 2022 437

Potential for transmission of sporadic Creutzfeldt–Jakob disease through peripheral routes

Authors: Kobayashi, Atsushi, Munesue, Yoshiko, Shimazaki, Taishi, Aoshima, Keisuke, Kimura, Takashi, Mohri, Shirou, Kitamoto, Tetsuyuki

Source: In Laboratory Investigation October 2021 101(10):1327-1330

System degeneration in an MM1-type sporadic Creutzfeldt-Jakob disease case with an unusually prolonged akinetic mutism state

Authors: Iwasaki, Yasushi, Mori, Keiko, Ito, Masumi, Kawai, Yoshinari, Akagi, Akio, Riku, Yuichi, Miyahara, Hiroaki, Kobayashi, Atsushi, Kitamoto, Tetsuyuki, Yoshida, Mari

Source: Prion. 15(1):12-20

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100137200416.0x000001&indx=1&recIds=ETOCvdc_100137200416.0x000001

Detection of cutaneous prion protein deposits could help diagnose GPI‐anchorless prion disease with neuropathy

Authors: Honda, Hiroyuki, Matsuzono, Kosuke, Satoh, Kota, Fujisawa, Masayoshi, Suzuki, Satoshi O., Furuyama, Chiaki, Kitamoto, Tetsuyuki, Fujimoto, Shigeru, Abe, Koji, Iwaki, Toru

Source: European journal of neurology. 28(6):2133-2137

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100124237001.0x000001&indx=1&recIds=ETOCvdc_100124237001.0x000001

Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case

Authors: Shintaku, Masayuki, Nakamura, Takeshi, Kaneda, Daita, Shinde, Akiyo, Kusaka, Hirofumi, Takeuchi, Atsuko, Kitamoto, Tetsuyuki

Source: Neuropathology. 41(3):206-213

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122959380.0x000001&indx=1&recIds=ETOCvdc_100122959380.0x000001

A case report of an individual with Creutzfeldt–Jakob disease characterized by prolonged isolated thalamic lesions and rare MM2-cortical-type pathology.

Authors: Kunii, Misako, Kishida, Hitaru, Tada, Mikiko, Okamoto, Mitsuo, Asano, Keiichiro, Nakamura, Haruko, Takahashi, Keita, Hashiguchi, Shunta, Kubota, Shun, Okubo, Masaki, Takeuchi, Hideyuki, Ueda, Naohisa, Satoh, Katsuya, Kitamoto, Tetsuyuki, Doi, Hiroshi, Tanaka, Fumiaki

Source: BMC Neurology; 11/22/2024, Vol. 24 Issue 1, p1-7, 7p

Subject Terms: DIFFUSION magnetic resonance imaging, TAU proteins, JAPANESE people, BRAIN diseases, CEREBROSPINAL fluid

Unsuccessful transmissions of atypical genetic Creutzfeldt–Jakob disease (PRNP p.T183A-129M) in transgenic mice.

Authors: Baiardi, Simone, Vargiu, Claudia Marina, Mohri, Shirou, Windl, Otto, Herms, Jochen, Capellari, Sabina, Kitamoto, Tetsuyuki, Parchi, Piero

Source: Acta Neuropathologica; 11/20/2024, Vol. 148 Issue 1, p1-4, 4p

Subject Terms: PRION diseases, CREUTZFELDT-Jakob disease, ALZHEIMER'S disease, TRANSGENIC mice, WESTERN immunoblotting, PRIONS

A Retrospective Cohort Study of a Newly Proposed Criteria for Sporadic Creutzfeldt–Jakob Disease.

Authors: Nonaka, Toshiaki, Ae, Ryusuke, Kosami, Koki, Tange, Hiroya, Kaneko, Miho, Nakagaki, Takehiro, Hamaguchi, Tsuyoshi, Sanjo, Nobuo, Nakamura, Yoshikazu, Kitamoto, Tetsuyuki, Kuroiwa, Yoshiyuki, Kasuga, Kensaku, Doyu, Manabu, Tanaka, Fumiaki, Abe, Koji, Murayama, Shigeo, Yabe, Ichiro, Mochizuki, Hideki, Matsushita, Takuya, Murai, Hiroyuki

Source: Diagnostics (2075-4418); Nov2024, Vol. 14 Issue 21, p2424, 14p

Subject Terms: MAGNETIC resonance imaging, PRION diseases, REPORTING of diseases, SENSITIVITY & specificity (Statistics), NEUROLOGICAL disorders

Diffusion-weighted magnetic resonance imaging in dura mater graft-associated Creutzfeldt-Jakob disease

Authors: Sakai, Kenji, Hamaguchi, Tsuyoshi, Sanjo, Nobuo, Murai, Hiroyuki, Iwasaki, Yasushi, Hamano, Tadanori, Honma, Mari, Noguchi-Shinohara, Moeko, Nozaki, Ichiro, Nakamura, Yosikazu, Kitamoto, Tetsuyuki, Harada, Masafumi, Mizusawa, Hidehiro, Yamada, Masahito

Source: In Journal of the Neurological Sciences 15 November 2020 418

α2,3 linkage of sialic acid to a GPI anchor and an unpredicted GPI attachment site in human prion protein

Authors: Kobayashi, Atsushi ^*, Hirata, Tetsuya, Nishikaze, Takashi, Ninomiya, Akinori, Maki, Yuta, Takada, Yoko, Kitamoto, Tetsuyuki, Kinoshita, Taroh ^*

Source: In Journal of Biological Chemistry 29 May 2020 295(22):7789-7798

Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease

Authors: Ikeda, Toshimasa, Iwasaki, Yasushi, Sakurai, Keita, Akagi, Akio, Riku, Yuichi, Mimuro, Maya, Miyahara, Hiroaki, Kitamoto, Tetsuyuki, Matsukawa, Noriyuki, Yoshida, Mari

Source: In Journal of the Neurological Sciences 15 January 2020 408

A Novel Combination of Prion Strain Co-Occurrence in Patients with Sporadic Creutzfeldt-Jakob Disease

Authors: Kobayashi, Atsushi, Iwasaki, Yasushi, Takao, Masaki, Saito, Yuko, Iwaki, Toru, Qi, Zechen, Torimoto, Ryouta, Shimazaki, Taishi, Munesue, Yoshiko, Isoda, Norikazu, Sawa, Hirofumi, Aoshima, Keisuke, Kimura, Takashi, Kondo, Hinako, Mohri, Shirou, Kitamoto, Tetsuyuki

Source: In The American Journal of Pathology June 2019 189(6):1276-1283

Clinicopathological findings of a long-term survivor of V180I genetic Creutzfeldt-Jakob disease

Authors: Hayashi, Yuichi, Iwasaki, Yasushi, Waza, Masahiro, Kato, Shinei, Akagi, Akio, Kimura, Akio, Inuzuka, Takashi, Satoh, Katsuya, Kitamoto, Tetsuyuki, Yoshida, Mari, Shimohata, Takayoshi

Source: Prion. 14(1):109-117

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122052289.0x000001&indx=1&recIds=ETOCvdc_100122052289.0x000001

A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset

Authors: Nomura, Taichi, Iwata, Ikuko, Naganuma, Ryoji, Matsushima, Masaaki, Satoh, Katsuya, Kitamoto, Tetsuyuki, Yabe, Ichiro

Source: Prion. 14(1):226-231

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122052306.0x000001&indx=1&recIds=ETOCvdc_100122052306.0x000001

Identification of intracerebral hemorrhage in the early‐phase of MM1+2C‐type sporadic Creutzfeldt–Jakob disease: A case report

Authors: Akagi, Akio, Iwasaki, Yasushi, Yamamoto, Akihiro, Matsuura, Hiroshi, Ikeda, Toshimasa, Mimuro, Maya, Riku, Yuichi, Miyahara, Hiroaki, Kitamoto, Tetsuyuki, Yoshida, Mari

Source: Neuropathology. 40(4):399-406

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100108410838.0x000001&indx=1&recIds=ETOCvdc_100108410838.0x000001