9.

柿田明美．脳・神経１（非腫瘍性）．組織病理アトラス 第７版．大橋健一，伊藤智雄，牛久哲男，笹島ゆう子，田中伸哉，都築豊徳（編集）、文光堂，東京．pp. – . total pages. 2025年　月　日．in press.

8.

Nakajima A, Hokari M, Yanagimura F, Saji E, Shimizu H, Toyoshima Y, Yanagawa K, Arakawa M, Yokoseki A, Wakasugi T, Okamoto K, Watanabe K, Minato K, Otsu Y, Nozawa Y, Kobayashi D, Sanpei K, Kikuchi H, Hirohata S, Awamori K, Nawata A, Yamada M, Takahashi H, Nishizawa M, Igarashi H, Sato N, Kakita A, Onodera O, Kawachi I. Long-term clinical landscape of spinal hypertrophic pachymeningitis with anti-neutrophil cytoplasmic antibody-associated vasculitis. Neurology, in press.

7.

Gabdulkhaev R, Shimizu H, Kanazawa M, Kuroha Y, Hasegawa A, Idezuka J, Tainaka K, Onodera O, Kakita A (epub 2024 Dec 12). Blood-brain barrier dysfunction in multiple system atrophy: a human postmortem study. Neuropathology, in press. doi:10.1111/neup.13021.

6.

Shibuma S, On J, Natsumeda M, Koyama A, Takahashi H, Watanabe J, Mitobe M, Nakata S, Tanaka Y, Tsukamoto Y, Okada M, Yoshimura J, Tada M, Shimizu H, Oya S, Murai J, Okamoto K, Kawashima H, Kakita A, Oishi M (2025 Apr; epub 2025 Jan 9). Diagnosis of leptomeningeal disease in diffuse midline gliomas by detection of H3F3A K27M mutation in circulating tumor DNA of cerebrospinal fluid. Pediatr Blood Cancer 2025; 72 (4): e31535. doi: 10.1002/pbc.31535.

5.

Ando S, Saito R, Kitahara S, Uemura M, Hatano Y, Watanabe M, Kato T, Ito Y, Nalini A, Ishihara T, Murayama S, Igarashi H, Kakita A, Onodera O (2025 Feb 26). “Chocolate chip sign” on susceptibility-weighted imaging: a novel neuroimaging biomarker for HTRA1-related cerebral small vessel disease. Neurol Genet 2025; 11 (2): e200237. doi:10.1212/NXG.0000000000200237.

4.

Hongo S, Ikeda T, Tada M, Aida R, Ozawa T, Lixin L, Hara N, Miyashita A, Nakajima T, Ichinose H, Ikeuchi T, Onodera O, Kakita A (2025 Feb). Clinicopathologic and biochemical features of an autopsied patient with hereditary spastic paraplegia carrying a GTP cyclohydrolase 1 mutation. Neuropathol Appl Neurobiol 2025; 51 (1): e70006. doi: 10.1111/nan.70006.

3.

Iida M, Tanaka M, Takagi T, Matsuki T, Kimura K, Shibata K, Kobayashi Y, Mizutani Y, Kuwamura H, Yamada K, Kitaura H, Kakita A, Sakakibara M, Asai N, Takahashi M, Asai M (2025 Feb; epub 2024 Dec 15). Girdin deficiency causes developmental and epileptic encephalopathy with hippocampal sclerosis and interneuronopathy. Epilepsia 2025; 66 (2): 599-617. doi: 10.1111/epi.18204.

2.

Hongo S, Shimizu H, Saji E, Nakajima A, Okamoto K, Kawachi I, Onodera O, Kakita A (2025 Feb 2; Epub 2024 Apr 7). Acute respiratory failure caused by brainstem demyelinating lesions in an older patient with an atypical relapsing autoimmune disorder. Neuropathology 2025; 45 (1): 3-12. doi: 10.1111/neup.12976.

1.

Saito Y, Sugai K, Iwasaki M, Sato N, Kakita A, Saito Y, Ohtsuki T, Sasaki M (2025 Jan; epub 2024 Nov 27). Surgical outcome and contributing presurgical evaluations in children with magnetic resonance imaging-negative epilepsy and periodic seizure cycles. Epilepsy Res 2025; 209: 107492. doi: 10.1016/j.eplepsyres.2024.107492.