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Page 1
Impact of Amyloid and Tau PET on Changes in Diagnosis and Patient Management.
Shimohama S, Tezuka T, Takahata K, Bun S, Tabuchi H, Seki M, Momota Y, Suzuki N, Morimoto A, Iwabuchi Y, Kubota M, Yamamoto Y, Sano Y, Shikimoto R, Funaki K, Mimura Y, Nishimoto Y, Ueda R, Jinzaki M, Nakahara J, Mimura M, Ito D. Shimohama S, et al. Among authors: nishimoto y. Neurology. 2023 Jan 17;100(3):e264-e274. doi: 10.1212/WNL.0000000000201389. Epub 2022 Sep 29. Neurology. 2023. PMID: 36175151
A novel mutation in the HTRA1 gene causes CARASIL without alopecia.
Nishimoto Y, Shibata M, Nihonmatsu M, Nozaki H, Shiga A, Shirata A, Yamane K, Kosakai A, Takahashi K, Nishizawa M, Onodera O, Suzuki N. Nishimoto Y, et al. Neurology. 2011 Apr 12;76(15):1353-5. doi: 10.1212/WNL.0b013e318215281d. Neurology. 2011. PMID: 21482952 No abstract available.
Characteristic features and progression of abnormalities on MRI for CARASIL.
Nozaki H, Sekine Y, Fukutake T, Nishimoto Y, Shimoe Y, Shirata A, Yanagawa S, Hirayama M, Tamura M, Nishizawa M, Onodera O. Nozaki H, et al. Among authors: nishimoto y. Neurology. 2015 Aug 4;85(5):459-63. doi: 10.1212/WNL.0000000000001803. Epub 2015 Jul 2. Neurology. 2015. PMID: 26138950
HTRA1-Related Cerebral Small Vessel Disease: A Review of the Literature.
Uemura M, Nozaki H, Kato T, Koyama A, Sakai N, Ando S, Kanazawa M, Hishikawa N, Nishimoto Y, Polavarapu K, Nalini A, Hanazono A, Kuzume D, Shindo A, El-Ghanem M, Abe A, Sato A, Yoshida M, Ikeuchi T, Mizuta I, Mizuno T, Onodera O. Uemura M, et al. Among authors: nishimoto y. Front Neurol. 2020 Jul 3;11:545. doi: 10.3389/fneur.2020.00545. eCollection 2020. Front Neurol. 2020. PMID: 32719647 Free PMC article. Review.
[A case of myasthenia gravis and myositis induced by nivolumab].
Konoeda F, Suzuki S, Nishimoto Y, Hoshino H, Takagi M. Konoeda F, et al. Among authors: nishimoto y. Rinsho Shinkeigaku. 2017 Jul 29;57(7):373-377. doi: 10.5692/clinicalneurol.cn-000991. Epub 2017 Jul 30. Rinsho Shinkeigaku. 2017. PMID: 28674287 Japanese.
651 results