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Watanabe M, Nakamura K, Saito R, Takeuchi A, Takahashi T, Onodera O, Kitamoto T, Kakita A (2023) V180I genetic Creutzfeldt-Jakob disease: an autopsied patient presenting severe degeneration of the inferior olivary nucleus with M2T prion strain. Neuropathology 43 (6): 479-485

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Aiba I, Hayashi Y, Shimohata T, Yoshida M, Saito Y, Wakabayashi K, Komori T, Hasegawa M, Ikeuchi T, Tokumaru AM, Sakurai K, Murayama S, Hasegawa K, Uchihara T, Toyoshima Y, Saito Y, Yabe I, Tanikawa S, Sugaya K, Hayashi K, Sano T, Takao M, Sakai M, Fujimura H, Takigawa H, Adachi T, Hanajima R, Yokota O, Miki T, Iwasaki Y, Kobayashi M, Arai N, Ohkubo T, Yokota T, Mori K, Ito M, Ishida C, Tanaka M, Idezuka J, Kanazawa M, Aoki K, Aoki M, Hasegawa T, Watanabe H, Hashizume A, Niwa H, Yasui K, Ito K, Washimi Y, Mukai E, Kubota A, Toda T, Nakashima K; J-VAC study group (2023) Clinical course of pathologically confirmed corticobasal degeneration and corticobasal syndrome. Brain Commun 5 (6): fcad296

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Tsukamoto Y, Natsumeda M, Takahashi H, Ueno A, Sakai K, Shida K, Seto H, Saito T, Shibuma K, Nakayama Y, Tanaka Y, Nakano T, Ohta A, Maruyama K, Okada M, Eda T, Yoneoka Y, Shimizu H, Okamoto K, Kakita A, Oishi M (2023) Clinical, imaging, and molecular features of radiation-induced glioblastomas developed more than 20 years after radiation therapy for intracranial germinomatous germ cell tumor: illustrative cases. J Neurosurg: Case Lessons 6 (16): CASE23361

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齋藤奈つみ,黒羽泰子,長谷川有香,他田真理,柿田明美,渡邊慶,髙橋哲哉 (2023) 転倒発作と反復する一過性の言語障害を呈したY69H変異型遺伝性トランスサイレチン型髄膜アミロイドーシスの一例. 臨床神経  63 (10): 650-655

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Kitahara S, Kanazawa M, Natsumeda M, Sato A, Ishikawa M, Hara K, Tabe H, Makino K, Okamoto K, Fujita N, Kakita A, Fujii Y, Onodera O (2023) Progressive conus medullaris lesions are suggestive of intravascular large B-cell lymphoma. Eur J Neurol 30 (10): 3236-3243

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Miyahara K, Hino M, Shishido R, Izumi R, Nagaoka A, Kakita A, Yabe H, Tomita H, Kunii Y (2023) Ethnicity-dependent effect of rs1799971 polymorphism on OPRM1 expression in the postmortem brain and responsiveness for antipsychotics. J Psychiatr Res 166: 10-16

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佐藤朋江,齋藤理恵,齊ノ内 信,目崎 直実,三浦 健,眞島卓弥,柿田明美 (2023) 口蓋振戦と致死性の両側声帯外転麻痺をきたした両側小脳歯状核梗塞の一剖検例. 臨床神経 63 (9): 572-576

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Shishido R, Kunii Y, Hino M, Izumi R, Nagaoka A, Hayashi H, Kakita A, Tomita H, Yabe H (2023) Evidence for increased DNA damage repair in the postmortem brain of the high stress-response group of schizophrenia. Front Psychiatry 14: 1183696

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Takahashi K, Kanekiyo K, Sakuda K, Muto Y, Iguchi M, Matsuda N, Hashimoto Y, Kanai K, Ogawa H, Hirase H, Kakita A, Bizen N, Takebayashi H, Kawaguchi Y, Uzuki M, Kitazume S (2023) Brain-specific glycosylation of PTPRZ marks a demyelination-associated astrocyte subtype. J Neurochem 166 (3): 547-559

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Takahashi H, Natsumeda M, On J, Watanabe J, Tada M, Shimizu H, Tsukamoto Y, Okada M, Oishi M, Takizawa J, Hayashi Y, Masaki Y, Kakita A, Fujii Y (2023) Administration of glucocorticoids prior to liquid biopsy dramatically reduces the detection rate of MYD88 L265P mutation in cerebrospinal fluid of primary CNS lymphoma patients. Leuk Lymphoma 64 (6): 1219-1222

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Ogata A, Yamada T, Hattori S, Ikenuma H, Abe J, Tada M, Ichise M, Suzuki M, Ito K, Kato T, Amaike K, Hirota T, Kakita A, Itami K, Kimura Y (2023) Development of a novel PET ligand, [11C]GO289 targeting CK2 expressed in the brain. Bioorg Med Chem Lett 90: 129327

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Matsui H, Ito S, Matsui H, Ito J, Gabdulkhaev R, Hirose M, Yamanaka T, Koyama A, Kato T, Tanaka M, Uemura N, Matsui N, Hirokawa S, Yoshihama M, Shimazawa A, Kubo S, Iwasaki K, Hasegawa M, Takahashi R, Hirai K, Kakita A, Onodera O (2023) Phosphorylation of a-synuclein at T64 results in distinct oligomers and exerts toxicity in models of Parkinson’s disease. Prog Natl Acad Sci USA 120 (23): e2214652120

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Tsukamoto Y, Natsumeda M, Takahashi H, On J, Seto D, Saitou T, Shibuya K, Ogura R, Ito J, Oishi M, Shimizu H, Okamoto K, Kakita A, Fujii Y (2023) Diffusely infiltrating gliomas with poor prognosis, TERT promotor mutations and histological anaplastic pleomorphic xanthoastrocytoma-like appearance classify as mesenchymal subtype of glioblastoma, IDH-wildtype by methylation analysis Neurosurgery Practice 4 (2): e00040

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Miyahara K, Hino M, Shishido R, Nagaoka A, Hayashi H, Kakita A, Yabe H, Yomita H, Kunii Y (2023) Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis. Transl Psychiatry 13 (1): 144

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Nakata S, Murai J, Okada M, Takahashi H, Findlay TH, Malebranche K, Parthasarathy A, Miyashita S, Gabdulkhaev R, Benkimoun I, Druillennec S, Chabi S, Hawkins E, Miyahara H, Tateishi K, Yamashita S, Yamada S, Saito T, On J, Watanabe J, Tsukamoto Y, Yoshimura J, Oishi M, Nakano T, Imamura M, Imai C, Yamamoto T, Takeshima H, Sasaki AT, Rodriguez FJ, Nobusawa S, Varlet P, Pouponnot C, Osuka S, Pommier Y, Kakita A, Fujii Y, Raabe EH, Eberhart CG, Natsumeda M (2023) Epigenetic upregulation of Schlafen11 renders WNT- and SHH-activated medulloblastomas sensitive to cisplatin. Neuro Oncol 25 (5): 899-912

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宮下哲典, 原 範和, 春⽇健作, 菊地正隆, 尾崎浩⼀, 新飯⽥俊平, 他⽥真理, 柿⽥明美, 池内 健 (2023) APOE の遺伝型とレアミスセンスバリアント:臨床応⽤への可能性.Dementia Jpn 37 (2): 239-249

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Ando K, Natsumeda M, Kawamura M, Shirakawa K, Okada M, Tsukamoto Y, Eda T, Watanabe J, Saito S, Takahashi H, Kakita A, Oishi M, Fujii Y (2023) Elevated ratio of type C lectin-like receptor 2 level and platelet count (C2PAC) aids in the diagnosis of post-operative venous thromboembolism in IDH-wildtype gliomas. Thrombosis Res 223: 36-43

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Zhou Y, Tada M, Cai Z, Andhey PS, Swain A, Miller KR, Gilfillan S, Artyomov MN, Takao M, Kakita A, Colonna M (2023) Human early-onset dementia caused by DAP12 deficiency reveals a unique signature of dysregulated microglia. Nat Immunol 24 (3): 545-557

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Fujita A, Kato M, Sugano H, Iimura Y, Suzuki H, Tohyama J, Fukuda M, Ito Y, Baba S, Okanishi T, Enoki H, Fujimoto A, Yamamoto A, Kawamura K, Kato S, Honda R, Ono T, Shiraishi H, Egawa K, Shirai K, Yamamoto S, Hayakawa I, Saida K, Tsuchida N, Uchiyama Y, Hamanaka K, Miyatake S, Mizuguchi T, Nakashima M, Saitsu H, Miyake N, Kakita A, Matsumoto N (2023) An integrated genetic analysis of epileptogenic brain malformed lesions. Acta Neuropathol Commun 11 (1): 33

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小柳清光、橋本智代、和田 学、山崎峰雄、中原亜紗、柿田明美 (2023) グアム島と西ニューギニアのALS(筋萎縮性側索硬化症)とは何であり、医学はそれらから何を学んだのか.Clin Neurosci 41 (3): 325-329

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Saito Y, Sugai K, Atobe M, Sato N, Kakita A, Saito Y, Ohtsuki T, Iwasaki M, Sasaki M (2023) Periodic cycles of seizure clustering and suppression in children strongly suggest focal cortical dysplasia. Dev Med Child Neurol 65 (3): 431-436

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Tojima M, Kobayashi K, Hitomi T, Ishibashi H, Yoshii D, Sainouchi M, Ayaki T, Shimotake A, Usami K, Maki T, Kakita A, Takahashi R, Ikeda A (2023) A super elderly autopsy case of benign adult familiar myoclonus epilepsy with a heterozygous mutation. Epileptic Disord 25 (1): 110-113

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Saito R, Hara N, Tada M, Wakabayashi M, Miyashita A, Onodera O, Ikeuchi T, Kakita A (2023) SYNE1-ataxia: clinicopathologic features of an autopsied patient with novel compound heterozygous mutations. J Neuropathol Exp Neurol 82 (3): 267-271

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Nomura K, Suzuki H, Iimura Y, Mitsuhashi T, Ueda T, Nishioka K, Fusegi K, Nakajima M, Kakita A, Sugano H (2023) Epilepsy surgery without lipoma removal for temporal lobe epilepsy associated with Sylvian fissure lipoma: a case report. Acta Neurochir (Wien) 165 (1): 265-269

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Sakai K, Noguchi-Shinohara M, Tanaka H, Ikeda T, Hamaguchi T, Kakita A, Yamada M, Ono K (2023) Cerebrospinal fluid biomarkers and Amyloid-b elimination from the brain in cerebral amyloid angiopathy-related inflammation. J Alzheimer Dis 2023; 91 (3): 1173-1183