33.

Yukawa T, Iwakura Y, Takei N, Saito M, Watanabe Y, Toyooka K, Igarashi M, Niizato K, Ohima K, Kunii Y, Yabe H, Matsumoto J, Wada A, Hino M, Iritani S, Niwa S, Takeuchi R, Takahashi H, Kakita A, Someya T, Nawa H (2018) Pathologic alterations of chondroitin sulfate moiety in the postmortem hippocampus of patients with schizophrenia. Psychiatry Res 270: 940-946

32.

Takahashi M, Kitaura H, Kakita A, Kakihana T, Katsuragi Y, Nameta M, Zhang L, Iwakura Y, Nawa H, Higuchi M, Komatsu M, Fujii M (2018) USP10 is a driver of ubiquitinated protein aggregation and aggresome formation to inhibit apoptosis. iScience 9: 433-450

31.

Motoki M, Nakajima H, Sato T, Tada M, Kakita A, Arawaka S (2018) Neuronal intranuclear inclusion disease showing intranuclear inclusions in renal biopsy 12 years earlier. Neurology 91 (19): 884-886

30.

Ito J, Shimada T, Tada M, Shimizu H, Wakabayashi M, Yokoseki A, Onodera O, Takahashi H, Kakita A (2018) Clinicopathologic features of two patients with sporadic amyotrophic lateral sclerosis who maintained communication ability for over 30 years. J Neuropathol Exp Neurol 77 (11): 981-986

29.

Hoshi A, Tsunoda A, Yamamoto T, Tada M, Kakita A, Ugawa Y (2018) Altered expressions of glutamate transporter-1 and water channel protein aquaporin-4 in human temporal cortex with Alzheimer’s disease. Neuropathol Appl Neurobiol 44 (6): 628-638

28.

Hirose T, Nobusawa S, Sugiyama K, Fujimoto N, Sasaki A, Mikami Y, Kakita A, Tanaka S, Yokoo H (2018) Astroblastoma: a distinct tumor entity characterized by alterations of the X chromosome and MN1 rearrangement. Brain Pathol 28 (5): 684-694

27.

Miki Y, Tanji K, Mori F, Utsumi J, Sasaki H, Kakita A, Takahashi H, Wakabayashi K (2018) Autophagy mediators (FOXO1, SESN3 and TSC2) in Lewy body disease and aging. Neurosci Lett 684: 35-41

26.

豊島靖子、柿田明美 (2018) 神経 (2) 変性・炎症．カラーアトラス 病理組織の見方と鑑別診断．第6版.（監修）赤木忠厚、松原修、真鍋俊明、（編集）吉野正、小田義直、坂元亨宇、森井英一．医歯薬出版，東京．pp. 473-505 (total 699 pages)

25.

Tainaka K, Murakami TC, Susaki EA, Shizimu C, Saito R, Takahashi K, Hayashi-Takagi A, Sekiya H, Arima Y, Nojima S, Ikemura M, Ushiku T, Shimizu Y, Murakami M, Tanaka KF, Lino M, Kasai H, Sasaoka T, Kobayashi K, Miyazono K, Morii E, Isa T, Fukayama M, Kakita A, Ueda HR (2018) Chemical landscape for tissue clearing based on hydrophilic reagents. Cell Reports 24 (8): 2196-2210.e9

24.

Ito J, Nozaki H, Toyoshima Y, Abe T, Sato A, Hashidate H, Igarashi S, Onodera O, Takahashi H, Kakita A (2018) Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation. Neuropathology 38 (4): 428-432

23.

Xu C, Li Q, Efimova O, He L, Tatsumoto S, Oishi T, Udono T, Yamaguchi K, Shigenobu S, Kakita A, Nawa H, Khaitovich P, Go Y (2018) Human-specific features of special gene expression and regulation in eight brain regions. Genome Res 28 (8): 1097-1110

22.

北浦弘樹、柿田明美 (2018) フラビン蛍光イメージングによるてんかん原性の解析．Clin Neurosci 36 (8): 970-972

21.

Suzuki Y, Nakamura Y, Yamada K, Kurabe S, Okamoto K, Aoki H, Kitaura H, Kakita A, Fujii Y, Huber VJ, Igarashi H, Kwee I, Nakada T (2018) Aquaporin PET differentiates between grade III and IV human astrocytoma. Neurosurgery 82 (6): 842-846

20.

Sumitomo N, Ishiyama A, Shibuya M, Nakagawa E, Kaneko Y, Takahashi A, Otsuki T, Kakita A, Saito Y, Sato N, Sugai K, Sasaki M (2018) Intractable epilepsy due to a rosette-forming glioneuronal tumor with dysembryoplastic neuroepithelial background. Neuropathology 38 (3): 300-304

19.

Matsumoto J, Nagaoka A, Kunii Y, Miura I, Hino M, Niwa S, Nawa H, Takahashi H, Kakita A, Yabe H (2018) Effects of the -141C insertion/deletion polymorphism in the dopamine D2 receptor gene on the dopamine system in the striatum in patients with schizophrenia. Psychiatry Res 264: 116-118

18.

齋藤理恵、伊藤慎治、野崎洋明、柿田明美 (2018) 遺伝性脳血管障害の神経病理．特集：神経病理：update. 神経内科 88 (5): 516-523

17.

田中英智、豊島靖子、柿田明美 (2018) Globular glial tauopathyの神経病理．特集：神経病理：update. 神経内科 88 (5): 477-482

16.

他田真理、柿田明美 (2018) 前頭側頭葉変性症の組織学的分類．特集：非アルツハイマー型認知症の病理学．Brain Nerve 70 (5): 501-516

15.

Ishiura H, Doi K, Mitsui J, Yoshimura J, Kawabe Matsukawa M, Toyoda A, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Yurino H, Higasa K, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Nakamoto F, Kanda J, Higashihara M, Abe K, Koike R, Sasagawa M, Kurohane Y, Hasegawa N, Kanazawa N, Kondo T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Sakiyama Y, Ohtsuka M, Ueki A, Kaida K, Shimizu J, Hanajima R, Hayashi T, Terao Y, Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Kira J, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita S, Tsuji S (2018) Intronic TTTCA and TTTTA repeat expansions in benign adult familial myoclonic epilepsy. Nat Genet 50 (4): 581-590

14.

Sugita Y, Furuta T, Ohshima K, Komaki S, Miyoshi J, Morioka M, Abe H, Tsukamoto Y, Takahashi H, Kakita A (2018) The perivascular microenvironment in Epstein-Barr virus positive primary central nervous system lymphoma: the role of programed cell death protein 1 and programed cell death ligand 1. Neuropathology 38 (2): 125-134

13.

Natsumeda M, Motohashi K, Igarashi H, Nozawa T, Abe H, Tsukamoto Y, Ogura R, Okada M, Kobayashi T, Aoki H, Takahashi H, Kakita A, Okamoto K, Nakada T, Fujii Y (2018) Reliable diagnosis of IDH-mutant glioblastoma by 2-hydroxyglutarate detection: a study by 3-T magnetic resonance spectroscopy. Neurosurg Rev 41 (2): 641-647

12.

Saito R, Tada M, Toyoshima Y, Nishizawa M, Onodera O, Takahashi H, Kakita A (2018) Motor neuron loss in the upper cervical cord in patients with multiple system atrophy and dropped head. J Neuropathol Exp Neurol 77 (4): 317-324

11.

Tanji K, Mori F, Miki Y, Utsumi J, Sasaki H, Kakita A, Takahashi H, Wakabayashi K (2018) YOD1 attenuates neurogenic protein-toxicity through deubiquitinating activity. Neurobiol Dis 112: 14-23

10.

Kitaura H, Shirozu H, Masuda H, Fukuda M, Fujii Y, Kakita A (2018) Pathophysiological characteristics of the subiculum associated with epileptogenesis in human hippocampal sclerosis. EBioMedicine 29: 38-46

9.

Kidana K, Tatebe T, Ito K, Hara N, Kakita A, Saito T, Ouchi Y, Ikeuchi T, Makino M, Saido TC, Akishita M, Iwatsubo T, Hori Y, Tomita T (2018) Astrocyte-derived kallikrein-related peptidese 7 attenuates amyloid-β pathology in brain. EMBO Mol Med 10 (3): e8184

8.

他田真理、柿田明美 (2018) ミクログリアの組織学的特徴. 臨床医のための神経病理 再入門. Clinical Neuroscience 36 (3): 276-277

7.

Yoneoka Y, Akiyama K, Seki Y, Hasegawa G, Kakita A (2018) Frontoethmoidal schwannoma with exertion cerebrospinal fluid rhinorrhea: a case report and review of the literature. World Neurosurg 111: 381-385

6.

Mutoh H, Kato M, Akita T, Shibata T, Wakamoto H, Ikeda H, Kitaura H, Aoto K, Nakashima M, Wang T, Ohba C, Miyatake S, Miyake N, Kakita A, Miyake K, Fukuda A, Matsumoto N, Saitsu H (2018) Biallelic variants in CNPY3, which encodes an endoplasmic reticulum chaperone, cause early-onset epileptic encephalaopathy. Am J Hum Genet 102 (2): 321-329

5.

Yokose M, Furuya K, Suzuki M, Ozawa T, Kim Y, Miura K, Matsuzono K, Mashiko T, Tada M, Koide R, Shimazaki H, Matsuura T, Fujimoto S (2018) Vertical Gaze Palsy Caused by Selective Unilateral Rostral Midbrain Infarction. Neuro-Ophthalmology 42: 309-311

4.

Yoneoka Y, Yoshimura J, Sano M, Okada M, Kakita A, Fujii Y (2018) Third ventricle germ cell tumor originating from the infundibulum with rapidly expansive enlargement. Pediatr Neurosurg 53 (1): 49-54

3.

Miki Y, Tanji K, Mori F, Tatara Y, Utsumi J, Sasaki H, Kakita A, Takahashi H, Fimia GM, Wakabayashi K (2018) AMBRA1, a novel α-synuclein-binding protein, is implicated in the pathogenesis of multiple system atrophy. Brain Pathology 28 (1): 28-42

2.

Kitamura Y, Komori T, Shibuya M, Ohara K, Saito Y, Hayashi S, Sasaki A, Nakagawa E, Tomio R, Kakita A, Nakatsukasa M, Yoshida K, Sasaki H (2018) Comprehensive genetic characterizeation of rosette-forming glioneuronal tumors: independent component analysis by tissue microdissection. Brain Pathology 28 (1): 87-93

1.

Mori F, Tanji F, Miki Y, Toyoshima Y, Sasaki H, Yoshida M, Kakita A, Takahashi H, Wakabayashi K (2018) Immunohistochemical localization of exoribonucleases (DIS3L2 and XRN1) in intranuclear inclusion body disease. Neurosci Lett 662: 389-394