Works matching AU Koide, Shin

Results: 4

Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying NOTCH2NLC Repeat Expansion.
Published in:
Brain Sciences (2076-3425), 2023, v. 13, n. 6, p. 955, doi. 10.3390/brainsci13060955
By:
- Fitrah, Yusran Ady;
- Higuchi, Yo;
- Hara, Norikazu;
- Tokutake, Takayoshi;
- Kanazawa, Masato;
- Sanpei, Kazuhiro;
- Taneda, Tomone;
- Nakajima, Akihiko;
- Koide, Shin;
- Tsuboguchi, Shintaro;
- Watanabe, Midori;
- Fukumoto, Junki;
- Ando, Shoichiro;
- Sato, Tomoe;
- Iwafuchi, Yohei;
- Sato, Aki;
- Hayashi, Hideki;
- Ishiguro, Takanobu;
- Takeda, Hayato;
- Takahashi, Toshiaki
Publication type:
Article
A patient with neuronal intranuclear inclusion disease developed encephalitis‐like symptoms after cerebral angiography.
Published in:
2025
By:
- Koide, Shin;
- Tsuboguchi, Shintaro;
- Koide, Shingo;
- Ninomiya, Itaru;
- Saito, Taiki;
- Ishiguro, Takanobu;
- Saji, Etsuji;
- Higuchi, Yo;
- Ikeuchi, Takeshi;
- Oishi, Makoto;
- Kanazawa, Masato;
- Onodera, Osamu
Publication type:
Case Study
Clinicopathologic features of two unrelated autopsied patients with Charcot-Marie-Tooth disease carrying MFN2 gene mutation.
Published in:
Acta Neuropathologica Communications, 2023, v. 11, n. 1, p. 1, doi. 10.1186/s40478-023-01692-w
By:
- Hayashi, Hideki;
- Saito, Rie;
- Tanaka, Hidetomo;
- Hara, Norikazu;
- Koide, Shin;
- Yonemochi, Yosuke;
- Ozawa, Tetsuo;
- Hokari, Mariko;
- Toyoshima, Yasuko;
- Miyashita, Akinori;
- Onodera, Osamu;
- Okamoto, Kouichirou;
- Ikeuchi, Takeshi;
- Nakajima, Takashi;
- Kakita, Akiyoshi
Publication type:
Article
Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49066-7
By:
- Chauvin, Samuel D.;
- Ando, Shoichiro;
- Holley, Joe A.;
- Sugie, Atsushi;
- Zhao, Fang R.;
- Poddar, Subhajit;
- Kato, Rei;
- Miner, Cathrine A.;
- Nitta, Yohei;
- Krishnamurthy, Siddharth R.;
- Saito, Rie;
- Ning, Yue;
- Hatano, Yuya;
- Kitahara, Sho;
- Koide, Shin;
- Stinson, W. Alexander;
- Fu, Jiayuan;
- Surve, Nehalee;
- Kumble, Lindsay;
- Qian, Wei
Publication type:
Article

Works matching AU Koide, Shin

Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying NOTCH2NLC Repeat Expansion.

A patient with neuronal intranuclear inclusion disease developed encephalitis‐like symptoms after cerebral angiography.

Clinicopathologic features of two unrelated autopsied patients with Charcot-Marie-Tooth disease carrying MFN2 gene mutation.

Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.