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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 (2022) Epigenetic upregulation of Schlafen11 renders WNT- and SHH- activated medulloblastomas sensitive to cisplatin. Neuro Oncol, noac243. in press

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Tanaka MT, Tanji K, Miki Y, Ozaki T, Mori F, Hayashi H, Kakita A, Wakabayashi K (2022) Phosphorylation of threonine 231 on tau in multiple system atrophy and its model mice. J Neuropathol Exp Neurol, in press

38.

Natsumeda M, Matsuzawa H, Watanabe M, Motohashi K, Gabdulkhaev R, Tsukamoto Y, Kanemaru Y, Watanabe J, Ogura R, Okada M, Kurabe S, Okamoto K, Kakita A, Igarashi H, Fujii Y (2022) SWI by 7T MR imaging for the microscopic imaging diagnosis of astrocytic and oligodendroglial tumors. AJNR Am J Neuroradiol, in press

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Nomura K, Suzuki H, Iimura Y, Mitsuhashi T, Ueda T, Nishioka K, Fusegi K, Nakajima M, Kakita A, Sugano H (2022) Epilepsy surgery without lipoma removal for temporal lobe epilepsy associated with Sylvian fissure lipoma: a case report. Acta Neurochir (Wien), in press

36.

Miki Y, Tanji K, Tanaka M, Altay F, Foti SC, Strand KM, Kon T, Shimoyama S, Furukawa T, Nishijima H, Asi YT, Bettencourt C, Jaumuktane Z, Tada M, Mori F, Yomiyama M, Lasgley T, Kakita A, Ling H, Lees AJ, Quinn N, Holton JL, Warner TT, Wakabayashi K (2022) The pathological substrate of memory impairment in multiple system atrophy. Mov Disord: e12844, in press

35.

Endo H, Tagai K, Ono M, Ikoma Y, Oyama A, Matsuoka K, Kokubo N, Hirata K, Sano Y, Oya M, Matsumoto H, Kurose S, Seki C, Shimizu H, Kakita A, Takahata K, Shinotoh H, Shimada H, Tokuda T, Kawamura K, Zhang M-R, Oishi K, Mori S, Takado Y, Higuchi M (2022) A machine learning-based approach for discrimination of tauopathies using [18F]OM-PBB3 PET images. images. Mov Disord, in press

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Saito Y, Sugai K, Atobe M, Sato N, Kakita A, Saito Y, Ohtsuki T, Iwasaki M, Sasaki M (2022) Periodic cycles of seizure clustering and suppression in children strongly suggest focal cortical dysplasia. Dev Med Child Neurol, in press

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Watabe K, Niida-Kawaguchi M, Tada M, Kato Y, Murata M, Tanji K, Wakabayashi K, Yamada M, Kakita A, Shibata N (2022) Praja1 RING-finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease-associated protein aggregation. Neuropathology, in press

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Saito S, Natsumeda M, Sainouchi M, Takino T, Shibuya K, On J, Kanemaru Y, Ogura R, Okada M, Oishi M, Shimada Y, Wakai T, Kakita A, Fujii Y (2022) Elucidating the multiple genetic alterations involved in the malignant transformation of a KRAS mutant neurenteric cyst: A case report. Neuropathology, in press

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Miyahara H, Akagi A, Otsuka Y, Sakai M, Sone J, Kuru S, Hasegawa M, Yoshida M, Kakita A, Iwasaki Y (2022) Secondary tauopathy following subacute sclerotic panencephalitis in autopsy cases treated with or without aggressive antiviral therapies. Brain Pathol 32 (6): e13069

30.

Matsuoka K, Ono M, Takado Y, Hirata K, Endo H, Ofuse T, Kojima T, Yamamoto T, Onishi T, Orihara A, Tagai K, Takahata K, Seki C, Shinotoh H, Kawamura K, Shimizu H, Shimada H, Kakita A, Zhang M-R, Suhara T, Higuchi M (2022) High-contrast imaging of a-synuclein pathologies in living patients with multiple system atrophy. Mov Disord 37 (10): 2159-2161

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Oyanagi K, Hayashi H, Yamada M, Kakita A (2022) The large neuron involvement in the neostriatum in Lewy body diseases. Neuropathology 42 (5): 459-463

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Tanaka MT, Miki Y, Bettencourt C, Ozaki T, Tanji K, Mori F, Kakita A, Wakabayashi K (2022) Involvement of autophagic protein DEF8 in Lewy bodies. Biochem Biophys Res Commun 623: 170-175

27.

Kuroha Y, Ishiguro T, Tada M, Hara N, Murayama K, Kawachi I, Kasuga K, Miyashita A, Hasegawa A, Takahashi T, Matsubara N, Onodera O, Kakita A, Koike R, Ikeuchi T (2022) Biallelic COX10 mutations and PMP22 deletion in a family with Leigh syndrome and hereditary neuropathy with liability to pressure palsy. Neurol Genet 8 (5): e200030

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Mouri Y, Natsumeda M, Okubo N, Sato T, Saito T, Shibuya K, Yamada S, On J, Tsukamoto Y, Okada M, Oishi M, Eda T, Murai J, Shimizu H, Kakita A, Fujii Y (2022) Successful treatment of acute uric acid nephropathy with rasburicase in a primary central nervous system lymphoma patient showing dramatic response to methotrexate – case report. J Clin Med 11: 5548

25.

Mori F, Nakamura Y, Miki Y, Tanji K, Kon T, Tomiyama M, Kakita A, Wakabayashi K (2022) Alteration of vesicle-associated membrane protein-binding protein B in a-synuclein aggregates in Lewy body disease. J Neuropathol Exp Neurol 81 (10): 807-815

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Sato T, Hiraishi T, Tada M, Natsumeda M, On J, Sasaki T, Kou N, Takahashi H, Saito T, Okubo N, Oishi M, Kakita A, Fujii Y (2022) Meningoencephalocele in the lateral sphenoid sinus with congenital abnormalities in the brain tissue: a case report. NMC Case Rep J 9: 281-287

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Matsuda K, Sugita Y, Furuta T, Muta H, Ohshima K, Morioka M, Takahashi K, Higaki K, Kakita A (2022) Elevated expression of transforming acidic coiled-coil containing protein 3 (TACC3) reflects aggressiveness of primary central nervous system lymphomas. Pathol Int 72 (9): 437-443

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Iwakura Y, Kawahara-Miki R, Kida S, Sotoyama H, Gabdulkhaev R, Takahashi H, Kunii Y, Hino M, Nagaoka A, Izumi R, Shishido R, Someya T, Yabe H, Kakita A, Nawa H (2022) Elevation of EGR1/zif268, a neural activity marker, in the auditory cortex of patients with schizophrenia and its animal model. Neurochem Res 47 (9): 2715-2727

20.

Takei N, Yokomaku D, Yamada T, Nagano T, Kakita A, Namba H, Ushiki T, Takahashi H, Nawa H (2022) EGF downregulates presynaptic maturation and suppresses synapse formation in vitro and in vivo. Neurochem Res 47 (9): 2632-2644

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Oyanagi K, Shimizu H, Yamada M, Kakita A (2022) The neostriatum in polyglutamine diseases: preferential decrease of large neurons in dentatorubural-pallidoluysian atrophy and Machado-Joseph disease, but of small neurons in Huntington disease. Neuropathology 42 (4): 274-281

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他田真理、柿田明美 (2022) ミクログリア関連疾患の病理 (HDLS, NHD, ALD).特集II/神経核内封入体病・白質脳症. 脳神経内科97 (1): 91-100

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齋藤理恵、柿田明美 (2022) 脳小血管病の病理.特集II/神経核内封入体病・白質脳症. 脳神経内科 97 (1): 81-90

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Nakamori M, Shimizu H, Ohawa K, Hasuike Y, Sakurai H, Araki T, Okada Y, Kakita A, Mochizuki H (2022) Cell type-specific abnormalities of central nervous system in myotonic dystrophy type 1. Brain Commun 4 (3): fcac154

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齋藤理恵,小野寺 理,柿田明美 (2022) CARASIL. 臨床医のための神経病理 再入門. Clin Neurosci 40 (6): 700-702

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Tanaka H, Shimizu H, Yonemochi Y, Ozawa T, Toyoshima Y, Nakajima T, Kakita A (2022) Fibrodysplasia ossifications progressive: histopathological implications of aberrant BMP signaling for CNS dysgenesis. Neuropathol Appl Neurobiol 48 (4): e12805

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柿田明美.神経病理への影響と課題.COVID-19 神経ハンドブック.−急性期,後遺症からワクチン副反応まで−.(編集)下畑享良.中外医学社, 東京. 2022,pp. 283-290

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Tsujikawa K, Hamanaka K, Sahashi K, Hattori Y, Hara N, Iguchi Y, Riku Y, Ishigaki S, Miyatake S, Mitsuhashi S, Miyazaki Y, Kataoka M, Jiayi L, Yasui K, Kura S, Koike H, Kobayashi K, Sahara N, Ozaki N, Yoshida M, Kakita A, Saito Y, Ikeuchi T, Japanese Longitudinal Biomarker Study in PSP and CBD (JALPAC) Consortium, Miyata T, Sobue G, Matsumoto N, Katsuno M (2022) Actin-binding protein-A drives tau aggregation and contributes to progressive supranuclear palsy pathology. Sci Adv 8 (21): eabm5029

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Kajikawa S, Matsuhashi M, Kobayashi K, Hitomi T, Daifu M, Kobayashi T, Yamao Y, Kikuchi T, Yoshida K, Kunieda T, Matsumoto R, Kakita A, Namiki T, Tsuda I, Takahashi R, Ikeda A (2022) Two types of ictal direct current shifts convinced by waveform property, cluster analysis and its pathology. Clin Neurophysiol 137: 113-121

10.

Ishihara T, Koyama A, hatano Y, Takeuchi R, Koike Y, Kato T, Tada M, Kakita A, Onodera O (2022) Endogenous human retrovirus-K is not increased in the affected tissues of Japanese ALS patients. Neurosci Res 178: 78-82

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Sakai K, Ishida C, Hayashi K, Kannon T, Hosomichi K, Takei N, Kakita A, Tajima A, Yamada M (2022) Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions. Neuropathology 42 (2): 126-133

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Sainouchi M, Tada M, Fitrah YA, Hara N, Tanaka K, Idezuka J, Aida I, Nakajima T, Miyashita A, Akazawa K, Ikeuchi T, Onodera O, Kakita A (2022) Brain TDP-43 pathology in corticobasal degeneration: topographical correlation with neuronal loss. Neuropathol Appl Neurobiol 48 (3): e12786

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Takahashi M, Kitaura H, Kakita A, Kakihana T, Katsuragi Y, Onodera O, Iwakura Y, Nawa H, Komatsu M, Fujii M (2022) USP10 inhibits aberrant cytoplasmic aggregation of TDP-43 by promoting stress granule clearance. Mol Cell Biol 42 (3): e0039321

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亀田知明,柿田明美 (2022) 脊髄梗塞.臨床医のための神経病理 再入門.Clin Neurosci 40 (3): 279-281

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Izumi R, Hino M, Nagaoka A, Shishido R, Kakita A, Hoshino M, Kunii Y, Yabe H (2022) Dysregulation of DPYSL2 expression by mTOR signaling in schizophrenia: multi-level study of postmortem brain. Neurosci Res 175: 73-81

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Kato M, Kada A, Shiraishi H, Tohyama J, Nakagawa E, Takahashi Y, Akiyama T, Kakita A, Miyake N, Fujita A, Saito AM, Inoue Y (2022) Sirolimus for epileptic seizures associated with focal cortical dysplasia type II. Ann Clin Transl Neurol 9 (2): 181-192

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佐藤朋江,齊ノ内信,齋藤理恵,柿田明美 (2022) 小脳・脳幹梗塞.臨床医のための神経病理 再入門.Clin Neurosci 40 (2): 148-150

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Inoue Y, Hamano S, Hayashi M, Sakuma H, Hirose S, Ishii A, Honda R, Ikeda A, Imai K, Jin K, Kada A, Kakita A, Kato M, Kawai K, Kawakami T, Kobayashi K, Matsuishi T, Matuo T, Nabatame S, Okamoto N, Ito S, Okumura A, Saito A, Shiraishi H, Shirozu H, Saito T, Sugano H, Takahashi Y, Yamamoto H, Fukuyama T, Kuki I (Japan Rare Epilepsy Syndrome Resistry Group; JRESG) (2022) Burden of seizures and comorbidities in patients with epilepsy: a survey based on the tertiary hospital-based Epilepsy Syndrome Registry in Japan. Epileptic Disord 24 (1): 82-94

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淡路正則,熊谷和樹,石川浩志,佐藤健,岡本浩一郎,柿田明美 (2022) 著明な嚢胞変性と骨破壊を伴った三叉神経鞘腫. 画像診断42 (2): 130-131