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Prion Volume 12, 2018 - Issue 1
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Research Paper

Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation

Akio AkagiDepartment of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Aichi, Japan;Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, Japan;Department of Neurology, National Hospital Organization Iou Hospital, Kanazawa, Ishikawa, Japan
,
Yasushi IwasakiDepartment of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Aichi, Japan
,
Maya MimuroDepartment of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Aichi, Japan
,
Tetsuyuki KitamotoDepartment of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan
,
Masahito YamadaDepartment of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, Japan
&
Mari YoshidaDepartment of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Aichi, JapanCorrespondence[email protected]
Pages 54-62 | Received 02 Oct 2017, Accepted 01 Dec 2017, Published online: 31 Jan 2018

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Taichi Nomura, Ikuko Iwata, Ryoji Naganuma, Masaaki Matsushima, Katsuya Satoh, Tetsuyuki Kitamoto & Ichiro Yabe. (2020) A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset. Prion 14:1, pages 226-231.
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Kenjiro Kunieda, Yuichi Hayashi, Megumi Yamada, Masahiro Waza, Tomonori Yaguchi, Ichiro Fujishima & Takayoshi Shimohata. (2020) Serial evaluation of swallowing function in a long-term survivor of V180I genetic Creutzfeldt-Jakob disease. Prion 14:1, pages 180-184.
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Yuichi Hayashi, Yasushi Iwasaki, Masahiro Waza, Shinei Kato, Akio Akagi, Akio Kimura, Takashi Inuzuka, Katsuya Satoh, Tetsuyuki Kitamoto, Mari Yoshida & Takayoshi Shimohata. (2020) Clinicopathological findings of a long-term survivor of V180I genetic Creutzfeldt-Jakob disease. Prion 14:1, pages 109-117.
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Yuichi Hayashi, Yasushi Iwasaki, Masahiro Waza, Hideaki Shibata, Akio Akagi, Akio Kimura, Takashi Inuzuka, Katsuya Satoh, Tetsuyuki Kitamoto, Mari Yoshida & Takayoshi Shimohata. (2019) Clinicopathological findings of an MM2-cortical-type sporadic Creutzfeldt-Jakob disease patient with cortical blindness during a course of glaucoma and age-related macular degeneration. Prion 13:1, pages 124-131.
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Articles from other publishers (10)

Masahiro Shijo, Motoi Yoshimura, Tsuyoshi Omae, Go Hashimoto, Tadataka Mizoguchi, Takahiro Kuwashiro, Takashi Komori, Yoshio Tsuboi, Tomoko Saito, Masanori Nakagawa, Kyoko Itoh & Hiroyuki Honda. (2023) Altered properties of amyloidogenic prion protein in genetic Creutzfeldt–Jakob disease with PRNP V180I mutation in response to pentosan polysulfate . Brain Pathology 33:5.
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Midori Watanabe, Kosei Nakamura, Rie Saito, Atsuko Takeuchi, Tetsuya Takahashi, Tetsuyuki Kitamoto, Osamu Onodera & Akiyoshi Kakita. (2023) V180I genetic Creutzfeldt‐Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain . Neuropathology.
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Ayano Shima, Kenji Sakai, Fumio Yamashita, Tsuyoshi Hamaguchi, Tetsuyuki Kitamoto, Makoto Sasaki, Masahito Yamada & Kenjiro Ono. (2023) 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. Journal of the Neurological Sciences 447, pages 120612.
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Dan Yeong Kim, Kyu Hwan Shim, Eva Bagyinszky & Seong Soo A. An. (2022) Prion Mutations in Republic of Republic of Korea, China, and Japan. International Journal of Molecular Sciences 24:1, pages 625.
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Taiki Matsubayashi & Nobuo Sanjo. (2022) Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt–Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene. International Journal of Molecular Sciences 23:23, pages 15172.
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Gianluigi Zanusso, Elisa Colaizzo, Anna Poleggi, Carlo Masullo, Raffaello Romeo, Sergio Ferrari, Matilde Bongianni, Michele Fiorini, Dorina Tiple, Luana Vaianella, Marco Sbriccoli, Flavia Porreca, Michele Equestre, Maurizio Pocchiari, Franco Cardone & Anna Ladogana. (2022) Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene. International Journal of Molecular Sciences 23:18, pages 10210.
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Takehiro Nakagaki, Miho Kaneko, Katsuya Satoh, Kiyohito Murai, Kazunobu Saiki, Gen Matsumoto, Keiko Ogami-Takamura, Kazuya Ikematsu, Akio Akagi, Yasushi Iwasaki, Toshiyuki Tsurumoto & Noriyuki Nishida. (2022) Detection of Prions in a Cadaver for Anatomical Practice. New England Journal of Medicine 386:23, pages 2245-2246.
Crossref
Thi-Thu-Trang Dong, Akio Akagi, Toshiaki Nonaka, Takehiro Nakagaki, Ban Mihara, Masaki Takao, Yasushi Iwasaki, Noriyuki Nishida & Katsuya Satoh. (2021) Formalin RT-QuIC assay detects prion-seeding activity in formalin-fixed brain samples from sporadic Creutzfeldt–Jakob disease patients. Neurobiology of Disease 159, pages 105504.
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Toshimasa Ikeda, Yasushi Iwasaki, Keita Sakurai, Akio Akagi, Yuichi Riku, Maya Mimuro, Hiroaki Miyahara, Tetsuyuki Kitamoto, Noriyuki Matsukawa & Mari Yoshida. (2020) Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease. Journal of the Neurological Sciences 408, pages 116515.
Crossref
Yasushi Iwasaki, Hiroko Kato, Tetsuo Ando, Akio Akagi, Maya Mimuro, Hiroaki Miyahara, Tetsuyuki Kitamoto & Mari Yoshida. (2018) Autopsy case of V180I genetic Creutzfeldt‐Jakob disease presenting with early disease pathology. Neuropathology 38:6, pages 638-645.
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