44.

Kanazawa M, Tada M, Onodera O, Takahashi H, Nishizawa M, Shimohata T (2013) Early clinical features of patients with progressive supranuclear palsy with predominant cerebellar ataxia. Parkinsonism Relat Disord 19: 1149-1151

43.

Mori F, Tanji K, Toyoshima Y, Sasaki H, Yoshida M, Kakita A, Takahashi H, Wakabayashi K (2013) Valosin-containing protein immunoreactivity in tauopathies, synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease. Neuropathology 33 (6): 637-644

42.

Takahashi H, Kakita A, Tomikawa M, Okamoto K, Kameyama S (2013) Oligodendroglioma (WHO grade I) in a young epilepsy patient: a specific entity lying within the spectrum of dysembryoplastic neuroepithelial tumor? Neuropathology 33 (6): 645-651

41.

豊島靖子, 高橋　均 (2013) 脳表ヘモジデリン沈着症の病理組織学的所見. 神経内科 79: 482-490

40.

Kagawa K, Iida K, Kakita A, Katagiri M, Nishimoto T, Hashizume A, Kiura Y, Hanaya R, Sugiyama K, Arihiro K, Arita K, Kurisu K (2013) Electrocorticographic-histopathologic correlations implying epileptogenicity of dysembryoplastic neuroepithelial tumor (DNT). Neurol Med Chir (Tokyo) 53: 676-687

39.

Ahmed Z, Bigio E, Budka H, Dickson DW, Ferrer I, Ghetti B, Giaccone G, Hatanpaa KJ, Holton JL, Josephs KA, Powers J, Spina S, Takahashi H, White III CL, Revesz T, Kovacs GG (2013) Globular glial tauopathies (GGT): consensus recommendations. Acta Neuropathol 126: 537-544

38.

Ishihara T, Ariizumi Y, Shiga A, Tan C-F, Sato T, Miki Y, Yokoo M, Fujino T, Koyama A, Yokoseki A, Nishizawa M, Kakita A, Takahashi H, Onodera O (2013) Decreased number of Gemini of coiled bodies and U12 snRNA level in amyotrophic lateral sclerosis. Hum Mol Genet 22: 4136-4147

37.

Nakayama Y, Watanabe M, Suzuki K, Usuda H, Emura I, Ogura R, Shiga A, Toyoshima Y, Takahashi H, Kawaguchi T, Kakita A (2013) Malignant peripheral nerve sheath tumor of the trigeminal nerve: clinicopathologic features in a young adult patient. Neuropathology 33 (5): 541-546

36.

Shimizu H, Yokoseki A, Shiga A, Toyoshima Y, Arakawa K, Sekine Y, Shimohata T, Ikeuchi T, Nishizawa M, Kakita A, Onodera O, Takahashi H (2013) Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene. Acta Neuropathol 126 (3): 453-459

35.

Kakita A (2013) Surgical pathologic features of cerebral cortical lesions taken from 600 patients with intractable epilepsy. Brain Dev 35: 793-801

34.

Nagayama S, Gondo Y, Araya S, Minato N, Fujita-Nakata M, Kaito M, Nakanishi M, Tanaka K, Yamaya H, Yokoyama H, Nakamichi K, Saijo M, Okamoto K, Toyoshima Y, Kakita A, Matsui M (2013) Progressive multifocal leukoencephalopathy developed 26 years after renal transplantation. Clin Neurol Neurosurg 115 (8): 1482-1484

33.

Kitaura H, Kakita A (2013) Optical imaging of human epileptogenic tissues in vitro. Neuropathology 33 (4): 469-474

32.

Ogura R, Aoki H, Natsumeda M, Shimizu H, Kobayashi T, Saito T, Takizawa J, Okamoto K, Hasegawa G, Umezu H, Ohshima K, Takahashi H, Fujii Y, Kakita A (2013) Epstein-Barr virus-associated primary central nervous system cytotoxic T-cell lymphoma. Neuropathology 33 (4): 436-441

31.

Takeuchi R, Toyoshima Y, Tada M, Shiga A, Tanaka H, Shimohata M, Kimura K, Morita T, Kakita A, Nishizawa M, Takahashi H (2013) Transportin 1 accumulates in FUS inclusions in adult-onset ALS without FUS mutation. Neuropathol Appl Neurobiol 39: 580-584

30.

The Multiple-Ststem Atrophy Research Collaboration. Jun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, Yoko Fukuda, Yaeko Ichikawa, Hidetoshi Date, Budrul Ahsan, Yasuo Nakahara, Yoshio Momose, Yuji Takahashi, Atsushi Iwata, Jun Goto, Yorihiro Yamamoto, Makiko Komata, Katsuhiko Shirahige, Kenju Hara, Akiyoshi Kakita,  Mitsunori Yamada, Hitoshi Takahashi, Osamu Onodera, Masatoyo Nishizawa, Hiroshi Takashima, Wataru Satake, Tatsushi Toda, Ryozo Kuwano, Hirohisa Watanabe, Mizuki Ito, Gen Sobue, Hiroyuki Soma, Ichiro Yabe, Hidenao Sasaki, Masashi Aoki, Kinya Ishikawa, Hidehiro Mizusawa, Kazuaki Kanai, Takamichi Hattori, Satoshi Kuwabara, Kimito Arai, Shigeru Koyano, Yoshiyuki Kuroiwa, Kazuko Hasegawa, Tatsuhiko Yuasa, Kenichi Yasui, Kenji Nakashima, Yuishin Izumi, Ryuji Kaji, Takeo Kato, Susumu Kusunoki, Yasushi Osaki, Masahiro Horiuchi, Tomoyoshi Kondo, Shigeo Murayama, Alexandra Dürr, Alexis Brice, Alessandro Filla, Thomas Klockgether, Ullrich Wüllner, Garth Nicolson, Sid Gilman, Caroline M. Tanner, Walter A. Kukull, Virginia M.-Y. Lee, Eliezer Masliah, Phillip A. Low, Paola Sandroni, John Q. Trojanowski, Laurie Ozelius, Tatiana Foroud, Shoji Tsuji (2013) Mutations of para-hydroxybenzoate-polyprenyltransferase gene (COQ2) are involved in familial and sporadic multiple system atrophy. N Engl J Med 369: 233-244

29.

Tanaka H, Shimazawa M, Takata M, Kaneko H, Tsuruma K, Ikeda T, Warita H, Aoki M, Yamada M, Takahashi H, Hozumi I, Minatsu H, Inuzuka T, Hara H (2013) ITIH4 and Gpx3 are potential biomarkers for amyotrophic lateral sclerosis. J Neurol 260: 1782-1797

28.

Suzuki K, Sato T, Yamada M, Takahashi H, Tsuji S (2013) DRPLA: recent advances in research using transgenic mouse model. Methods Mol Biol 1010: 277-292

27.

豊島靖子, 高橋　均 (2013) III. ALS と関連運動ニューロン疾患. ALS と FTLD. 辻　省次, 祖父江元 (編) アクチャル 脳・神経疾患の臨床, すべてがわかる ALS・運動ニューロン疾患, 中山書店, 東京, pp 75-82

26.

Eda T, Mizuno M, Araki K, Iwakura Y, Namba H, Sotoyama H, Kakita A, Takahashi H, Sato H, Chan S-Y, Nawa H (2013) Neurobehavioral deficits of epidermal growth factor-overexpressing transgenic mice: impact on dopamine metabolism. Neuroscience Letters 547: 21-25

25.

吉原章王, 榎本　雪, 高橋　均, 宇川義一 (2013) Gliomatosis cerebri の誘発電位検査. 神経内科 78: 726-728

24.

小池佑佳、大内東香、佐藤朋江、新保淳輔、佐藤晶、佐々木修、渋谷宏行、岡本浩一郎、柿田明美、五十嵐修一 (2013) MRIで髄膜造影を呈し脳生検で診断した脳アミロイドβ関連血管炎の１例．Brain Nerve 65: 693-697

23.

吉村淳一, 棗田　学, 西平　靖, 西山健一, 斎藤明彦, 岡本浩一郎, 高橋　均, 藤井幸彦 (2013) 白血病に対する全脳脊髄照射後に頭蓋内外に進展する骨肉腫を生じた Li-Fraumeni 類縁症候群の 1 例. 脳神経外科 41: 499-505

22.

Fu Y-J, Taniguchi Y, Takeuchi S, Shiga A, Okamoto K, Hirato J, Nobusawa S, Nakazato Y, Kakita A, Takahashi H (2013) Cerebral astroblastoma in an adult: an immunohistochemical, ultrastructural and genetic study. Neuropathology 33 (3): 312-319

21.

Miyahara H, Natsumeda M, Shiga A, Aoki H, Toyoshima Y, Zheng Y, Takeuchi R, Murakami H, Masuda H, Kameyama S, Izumi T, Fujii Y, Takahashi H, Kakita A (2013) Suppressed expression of autophagosomal protein LC3 in cortical tubers of tuberous sclerosis complex. Brain Pathol 23: 254-262

20.

柿田明美 (2013) 病理診断マニュアル．II. 診断マニュアル．(編) 大槻泰介，須貝研司，小国弘量，井上有史，永井利三郎．稀少難治てんかん診療マニュアル．診断と治療社．東京．pp. 114-116. total 170 pages

19.

柿田明美 (2013) 限局性皮質異形成．I. 疾患の特徴と診断のポイント．(編) 大槻泰介，須貝研司，小国弘量，井上有史，永井利三郎．稀少難治てんかん診療マニュアル．診断と治療社．東京．pp. 65-67. total 170 pages

18.

Ito T, Sawakami K, Ichikawa S, Hirano T, Endo N, Kakita A, Takahashi H (2013) Progression of paralysis is the most useful factor for differentiating malignant from benign intramedullary tumors. Spinal Cord 51 (4): 319-321

17.

Uemura M, Kosaka T, Shimohata T, Ishikawa M, Nishihira Y, Toyoshima Y, Yanagawa K, Kawachi I, Takahashi H, Nishizawa M (2013) Dropped head syndrome in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener 14: 232-233

16.

Wakabayashi K, Tanji K, Odagiri S, Miki Y, Mori F, Takahashi H (2013) The Lewy body in Parkinson’s disease and related neurodegenerative disorders. Mol Neurobiol 47: 495-508

15.

Kimura A, Sakurai T, Yoshikura N, Hayashi Y, Takemura M, Takahashi H, Inuzuka T (2013) Corticosteroid therapy in a patient with cerebral amyloid angiopathy-related inflammation. J Neuroinflammation 10:39

14.

豊島靖子, 山田光則, 高橋　均 (2013) IV. 小脳障害の病態. 小脳変性症の病理. 辻　省次, 西澤正人豊 (編) アクチャル 脳・神経疾患の臨床, 小脳と運動失調 小脳はなにをしているのか, 中山書店, 東京, pp 125-136

13.

Takahashi M, Obayashi M, Ishiguro T, Sato N, Niimi Y, Ozaki K, Mogushi K, Mahmut Y, Tanaka H, Tsuruta F, Dolmetsch R, Yamada M, Takahashi H, Kato T, Mori O, Eishi Y, Mizusawa H, Ishikawa K (2013) Cytoplasmic location of α1A voltage-gated calcium channel C-terminal fragment (Ca_v2.1-CTF) aggregate is sufficient to cause cell death. PLoS One 8: e50121

12.

Sasaki H, Matsushima M, Hama Y, Sakushima K, Nakamura M, Yabe I, Oba K, Tanji K, Mori F, Wakabayashi K, Kakita A, Takahashi H, Utsumi J (2013) Plasma matrix metalloproteinase-3 correlates with the clinical severity in men with multiple system atrophy. Neurology and Clinical Neuroscience 1 (2): 69-77

11.

Sakamoto M, Yasutake A, Kakita A, Ryufuku M, Chan HM, Yamamoto M, Oumi S, Kobayashi S, Watanabe C (2013) Selenomethionine protects against neuronal degeneration by methylmercury in the developing rat cerebrum. Environ Sci Technol 47: 2862-2868

10.

Hiraishi T, Kitaura H, Oishi M, Fukuda M, Kameyama S, Takahashi H, Kakita A, Fujii Y (2013) Significance of horizontal propagation of synchronized activities in human epileptic neocortex investigated by optical imaging and immunohistological study. Epilepsy Research 104 (1/2): 59-67

9.

Konno T, Shiga A, Tsujino A, Sugai A, Kato T, Kanai K, Yokoseki A, Eguchi H, Kuwabara S, Nishizawa M, Takahashi H, Onodera O (2013) Japanese amyotrophic lateral sclersois patients with GGGGCC hexanucleotide repeat expansion in C90RF72. J Neurol Neurosurg Psychiatry 84: 398-401

8.

Kosaka T, Kuroha Y, Tada M, Hasegawa A, Tani T, Matsubara N, Koike R, Toyoshima Y, Takahashi H (2013) A fatal neuromuscular disease in an adult patient after poliomyelitis in early childhood: consideration of the pathology of post-polio syndrome. Neuropathology 33: 93-101

7.

Tanaka S, Syu A, Ishiguro H, Inada T, Horiuchi Y, Ishikawa M, Koga M, Noguchi E, Ozaki N, Someya T, Kakita A, Takahashi H, Nawa H, Arinami T (2013) DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia. Pharmacogenomics J 13: 27-34

6.

Saji E, Arakawa M, Yanagawa K, Toyoshima Y, Yokoseki A, Okamoto K, Otsuki M, Akazawa K, Kakita A, Takahashi H, Nishizawa M, Kawachi I (2013) Cognitive impairment and cortical degeneration in neuromyelitis optica. Ann Neurol 73: 65-76

5.

Yoneda Y, Haginoya K, Kato M, Osaka H, Yokochi K, Arai H, Kakita A, Yamamoto T, Otsuki Y, Shimizu S, Wada T, Koyama N, Mino Y, Kondo N, Takahashi S, Hirabayashi S, Takanashi J, Okumura A, Kumagai T, Hirai S, Nabetani M, Saito S, Hattori A, Yamasaki M, Kumakura A, Sugo Y, Nishiyama K, Miyatake S, Tsurusaki Y, Doi H, Miyake N, Matsumoto N, Saitsu H (2013) Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephaly. Ann Neurol 73: 48-57

4.

Odagiri S, Tanji K, Mori F, Miki Y, Kakita A, Takahashi H, Wakabayashi K (2013) Brain expression level and activity of HDAC6 protein in neurodegenerative dementia. Biochem Biophys Res Commun 430: 394-399

3.

Tanji K, Odagiri S, Mori F, Kakita A, Takahashi H, Wakabayashi K (2013) Alteration of autophagosomal proteins in the brain of multiple system atrophy. Neurobiol Dis 49: 190-198

2.

Tanji K, Maruyama A, Odagiri S, Mori F, Itoh K, Kakita A, Takahashi H, Wakabayashi K (2013) Keap1 is localized in neuronal and glial cytoplasmic inclusions in various neurodegenerative diseases. J Neuropathol Exp Neurol 72 (1): 18-28

1.

Wen Y, Miyashita A, Kitamura N, Tsukie T, Saito Y, Hatsuta H, Murayama S, Kakita A, Takahashi H, Akatsu H, Yamamoto T, Kosaka K, Yamaguchi H, Akazawa K, Ihara Y, Kuwano R (2013) SORL1 is genetically associated with neuropathologically characterized late-onset Alzheimer’s disease. J Alzheimers Dis 35: 387-394