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Kon T, Miki Y, Tanji , Mori F, Tomiyama M, Toyoshima Y, Kakita A, Takahashi H, Utsumi , Sasaki H, Wakabayashi K (2015) Localization of nuclear receptor subfamily 4, group A, member 3 (NR43) in Lew body disease and multiple system atrophy. Neuropathology, 35 (6): 503-509
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Mori F, Miki , Tanji K, Kakita A, Takahashi H, Utsumi J, Sasaki , Wakabayashi K (2015) Sortilin-related receptor CNS expressed 2 (SorCS2) is localized to Bunina bodies in amyotrophic lateral sclerosis. Neurosci Lett 608: 6-11
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柿田明美 (2015) 海馬硬化.第3章 てんかんの病理学.In: 臨床てんかん学(編集:兼本浩祐、丸 栄一、池田昭夫、川合謙介).医学書院.東京,pp. 23-28 (total 671 p)
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Kimura T, Kitaura H, Masuda H, Kameyama S, Saito Y, Otsuki T, Nakazawa A, Morota N, Yamamoto T, Iida K, Takahashi H, Kakita A (2015) Characteristic p57/Kip2 immunoreactivity of balloon cells in focal cortical dysplasia. Neuropathology 35 (5): 401-409
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Bertolin G, Jacoupy M, Traver S, Ferrando-Miguel R, Saint Georges T, Grenier K, Ardila-Osorio H, Muriel MP, Takahashi H, Lees AJ, Gautier C, Guedin D, Coge F, Fon EA, Brice A, Corti O (2015) Parkin maintains mitochondrial levels of the protective Parkinson’s disease-related enzyme 17-β hydroxysteroid dehydrogenase type 10. Cell Death Differ 22: 1563-1576
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Kasai S, Torii S, Kakita A, Sogawa K (2015) Inhibitory PAS domain protein (IPAS) is a substrate of PINK1 and Parkin and mediates cell death in a Parkinson’s disease model. Cell Death Dis e1886
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Nakashima M, Saitsu H, Takei N, Tohyama J, Kato M, Kitaura H, Shiina M, Shirozu H, Masuda H, Watanabe K, Ohba C, Tsurusaki Y, Miyake N, Takebayashi H, Ogata K, Kameyama S, Kakita A, Matsumoto N (2015) Somatic mutations in the MTOR gene cause focal cortical dysplasia type IIb. Ann Neurol 78 (3): 375-386
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Ogura R, Tsukamoto Y, Natsumeda M, Isogawa M, Aoki H, Kobayashi T, Yoshida S, Okamoto K, Takahashi H, Fujii Y, Kakita A (2015) Immunohistochemical profiles of IDH1, MGMT and p53: practical significance for prognostification of patients with diffuse gliomas. Neuropathology 35 (4): 324-335
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Sakai M, Watanabe Y, Someya T, Araki K, Shibuya M, Niizato K, Oshima K, Kunii Y, Yabe H, Matsumoto J, Wada A, Hino M, Hashimoto T, Hishimoto A, Kitamura N, Iritani S, Shirakawa O, Maeda K, Miyashita A, Niwa S, Takahashi H, Kakita A, Kuwano R, Nawa H (2015) Assessment of copy number variations in the brain genome of schizophrenia patients. Mol Cytogenet 8: 46
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黒羽泰子, 他田真理, 河内 泉, 西澤正豊, 松原奈絵, 小池亮子 (2015) ピルビン酸ナトリウム療法が有効であったm.3271T>C点変異を有するミトコンドリア病の1例. 臨床神経 55: 412-416
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Oyanagi K, Yamazaki M, Hashimoto T, Akasawa M, Wakabayashi K, Takahashi H (2015) Hippocampal sclerosis in the parkinsonism-dementia complex of Guam: quantitative examination of neurons, neurofibrillary tangles, and TDP-43 immunoreactivity in CA1. Neuropathology 35: 224-235
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Fukasawa T, Kubota T, Negoro T, Maruyama S, Honda R, Saito Y, Ito M, Kakita A, Sugai K, Otsuki T, Natsume J, Watanabe K (2015) Two siblings with cortical dysplasias: focal cortical dysplasia and hemimegalencephaly: clinicoencephalographic features. Pediatr Int 57 (3): 472-475
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Morota N, Kumabe T, Kakita A (2015) Posterior fossa choroid plexus tumor. Chapter 48, In: Ozek MM, Cinalli G, Maixner WJ, Saint-Rose C (eds). Tumors of the Posterior Fossa in Children. Springer International Publishing, Switzerland. pp. 723-743 (total pp. 931)
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Yajima R, Toyoshima Y, Wada Y, Takahashi T, Arakawa H, Ito G, Kobayashi D, Yamada M, Kawachi I, Narita I, Takahashi H, Nishizawa M (2015) A fulminant case of granulomatosis with polyangiitis with meningeal and parenchymal involvement. Case Rep Neurol 7: 101-104
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柿田明美 (2015) 髄鞘病変を鑑別するポイント.神経病理診断の標準化II.病理と臨床 33巻4号, 文光堂,東京,pp. 352-358
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Kaneko M, Noguchi T, Ikegami S, Sakurai T, Kakita A, Toyoshima Y, Kambe T, Yamada M, Inden M, Hara H, Oyanagi K, Inuzuka T, Takahashi H, Hozumi I (2015) Zinc transporters (ZnT3 and T6) are downregulated in the spinal cord of patients with sporadic amyotrophic lateral sclerosis. J Neurosci Res 93 (2): 370-379
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