1. Aberrant astrocyte Ca2+ signals "AxCa signals" exacerbate pathological alterations in an Alexander disease model. Issue 5 (31st January 2018) Authors: Saito, Kozo; Shigetomi, Eiji; Yasuda, Rei; Sato, Ryuichi; Nakano, Masakazu; Tashiro, Kei; Tanaka, Kenji F.; Ikenaka, Kazuhiro; Mikoshiba, Katsuhiko; Mizuta, Ikuko; Yoshida, Tomokatsu; Nakagawa, Masanori; Mizuno, Toshiki; Koizumi, Schuichi Journal: Glia Issue: Volume 66:Issue 5(2018) Page Start: 1053 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Activation of a Cryptic Splice Site of GFAP in a Patient With Adult-Onset Alexander Disease. (1st December 2021) Authors: Amano, Eiichiro; Yoshida, Tomokatsu; Mizuta, Ikuko; Oyama, Jun; Sakashita, Shingo; Ueyama, Syunsuke; Machida, Akira; Yokota, Takanori Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Activation of a Cryptic Splice Site of GFAP in a Patient With Adult-Onset Alexander Disease. (December 2021) Authors: Amano, Eiichiro; Yoshida, Tomokatsu; Mizuta, Ikuko; Oyama, Jun; Sakashita, Shingo; Ueyama, Syunsuke; Machida, Akira; Yokota, Takanori Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Adult-onset leukoencephalopathy with homozygous LAMB1 missense mutation. (August 2020) Authors: Yasuda, Rei; Yoshida, Tomokatsu; Mizuta, Ikuko; Watanabe, Masashi; Nakano, Masakazu; Sato, Ryuichi; Tokuda, Yuichi; Omi, Natsue; Sakai, Norio; Nakagawa, Masanori; Tashiro, Kei; Mizuno, Toshiki Journal: Neurology Issue: Volume 6:Number 4(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An autopsy case of corticobasal syndrome due to asymmetric degeneration of the motor cortex and substantia nigra with TDP‐43 proteinopathy, associated with Alzheimer's disease pathology. Issue 3 (3rd February 2021) Authors: Tando, So; Kasai, Takashi; Mizuta, Ikuko; Takahashi, Hisashi; Yaoi, Takeshi; Saito, Kozo; Hojo, Tomohito; Mizuno, Toshiki; Hasegawa, Masato; Itoh, Kyoko Journal: Neuropathology Issue: Volume 41:Issue 3(2021) Page Start: 214 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS). Issue 4 (August 2018) Authors: Taki, Masakatsu; Nakamura, Takashi; Matsuura, Hiraku; Hasegawa, Tatsuhisa; Sakaguchi, Hirofumi; Morita, Kanako; Ishii, Ryotaro; Mizuta, Ikuko; Kasai, Takashi; Mizuno, Toshiki; Hirano, Shigeru Journal: Auris nasus larynx Issue: Volume 45:Issue 4(2018) Page Start: 866 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Characteristic abnormal signals in medulla oblongata—"eye spot" sign. Issue 3 (June 2015) Authors: Yoshida, Tomokatsu; Mizuta, Ikuko; Saito, Kozo; Kimura, Yasuyoshi; Park, Kwiyoung; Ito, Yasuo; Haji, Shotaro; Nakagawa, Masanori; Mizuno, Toshiki Journal: Neurology Issue: Volume 5:Issue 3(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Clinical and radiological characteristics of older‐adult‐onset Alexander disease. (19th July 2021) Authors: Yoshida, Tomokatsu; Mizuta, Ikuko; Yasuda, Rei; Mizuno, Toshiki Journal: European journal of neurology Issue: Volume 28:Number 11(2021) Page Start: 3760 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Definite familial multiple system atrophy with unknown genetics. Issue 3 (7th January 2014) Authors: Itoh, Kyoko; Kasai, Takashi; Tsuji, Yukiko; Saito, Kozo; Mizuta, Ikuko; Harada, Yoshinori; Sudoh, Shinji; Mizuno, Toshiki; Nakagawa, Masanori; Fushiki, Shinji Journal: Neuropathology Issue: Volume 34:Issue 3(2014) Page Start: 309 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL. (24th May 2016) Authors: Nozaki, Hiroaki; Kato, Taisuke; Nihonmatsu, Megumi; Saito, Yohei; Mizuta, Ikuko; Noda, Tomoko; Koike, Ryoko; Miyazaki, Kazuhide; Kaito, Muichi; Ito, Shoichi; Makino, Masahiro; Koyama, Akihide; Shiga, Atsushi; Uemura, Masahiro; Sekine, Yumi; Murakami, Ayuka; Moritani, Suzuko; Hara, Kenju; Yokoseki... Journal: Neurology Issue: Volume 86:Number 21(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗