Izumi Y - Search Results

1

The identification of raft-derived tau-associated vesicles that are incorporated into immature tangles and paired helical filaments.

Nishikawa T, Takahashi T, Nakamori M, Hosomi N, Maruyama H, Miyazaki Y, Izumi Y, Matsumoto M. Nishikawa T, et al. Among authors: izumi y. Neuropathol Appl Neurobiol. 2016 Dec;42(7):639-653. doi: 10.1111/nan.12288. Epub 2015 Dec 2. Neuropathol Appl Neurobiol. 2016. PMID: 26501932

2

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).

Matsuyama Z, Kawakami H, Maruyama H, Izumi Y, Komure O, Udaka F, Kameyama M, Nishio T, Kuroda Y, Nishimura M, Nakamura S. Matsuyama Z, et al. Among authors: izumi y. Hum Mol Genet. 1997 Aug;6(8):1283-7. doi: 10.1093/hmg/6.8.1283. Hum Mol Genet. 1997. PMID: 9259274

3

Lack of an association of estrogen receptor alpha gene polymorphisms and transcriptional activity with Alzheimer disease.

Maruyama H, Toji H, Harrington CR, Sasaki K, Izumi Y, Ohnuma T, Arai H, Yasuda M, Tanaka C, Emson PC, Nakamura S, Kawakami H. Maruyama H, et al. Among authors: izumi y. Arch Neurol. 2000 Feb;57(2):236-40. doi: 10.1001/archneur.57.2.236. Arch Neurol. 2000. PMID: 10681083 Clinical Trial.

4

Genetic studies in Parkinson's disease with an alpha-synuclein/NACP gene polymorphism in Japan.

Izumi Y, Morino H, Oda M, Maruyama H, Udaka F, Kameyama M, Nakamura S, Kawakami H. Izumi Y, et al. Neurosci Lett. 2001 Mar 9;300(2):125-7. doi: 10.1016/s0304-3940(01)01557-9. Neurosci Lett. 2001. PMID: 11207390

5

[Spinocerebellar ataxia type 8(SCA 8)].

Izumi Y, Maruyama H, Kawakami H. Izumi Y, et al. No To Shinkei. 2001 Jan;53(1):34-40. No To Shinkei. 2001. PMID: 11211728 Review. Japanese. No abstract available.

6

Influence of interleukin-1beta gene polymorphism on age-at-onset of spinocerebellar ataxia 6 (SCA6) in Japanese patients.

Nishimura M, Kawakami H, Maruyama H, Izumi Y, Kuno S, Kaji R, Nakamura S. Nishimura M, et al. Among authors: izumi y. Neurosci Lett. 2001 Jul 13;307(2):128-30. doi: 10.1016/s0304-3940(01)01934-6. Neurosci Lett. 2001. PMID: 11427317

7

Lack of an association between cystatin C gene polymorphisms in Japanese patients with Alzheimer's disease.

Maruyama H, Izumi Y, Oda M, Torii T, Morino H, Toji H, Sasaki K, Terasawa H, Nakamura S, Kawakami H. Maruyama H, et al. Among authors: izumi y. Neurology. 2001 Jul 24;57(2):337-9. doi: 10.1212/wnl.57.2.337. Neurology. 2001. PMID: 11468325

8

Guillain-Barré syndrome in a local area in Japan, 2006-2015: an epidemiological and clinical study of 108 patients.

Matsui N, Nodera H, Kuzume D, Iwasa N, Unai Y, Sakai W, Miyazaki Y, Yamazaki H, Osaki Y, Mori A, Furukawa T, Tsukamoto-Miyashiro A, Shimatani Y, Yamasaki M, Izumi Y, Kusunoki S, Arisawa K, Kaji R. Matsui N, et al. Among authors: izumi y. Eur J Neurol. 2018 May;25(5):718-724. doi: 10.1111/ene.13569. Epub 2018 Mar 1. Eur J Neurol. 2018. PMID: 29337417

9

Clinical and Pathological Features of FTDP-17 with MAPT p.K298_H299insQ Mutation.

Morino H, Kurashige T, Matsuda Y, Ono M, Sahara N, Miyasaka T, Soeda Y, Shimada H, Yamazaki Y, Takahashi T, Izumi Y, Ito H, Maruyama H, Higuchi M, Arihiro K, Suhara T, Takashima A, Kawakami H. Morino H, et al. Among authors: izumi y. Mov Disord Clin Pract. 2024 Jun;11(6):720-727. doi: 10.1002/mdc3.14042. Epub 2024 Apr 11. Mov Disord Clin Pract. 2024. PMID: 38605589

10

Time-course assessment of oral intake function and its impact on end-of-life in older individuals over 90 years with frailty.

Yamada H, Nakamori M, Oda M, Toko M, Sakahara H, Tagane Y, Yamazaki Y, Izumi Y, Maruyama H. Yamada H, et al. Among authors: izumi y. Geriatr Gerontol Int. 2025 Jan;25(1):96-101. doi: 10.1111/ggi.15048. Epub 2024 Dec 11. Geriatr Gerontol Int. 2025. PMID: 39659281

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