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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.
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 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.
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
684 results