Komure O - Search Results

1

A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease.

Morino H, Kawarai T, Izumi Y, Kazuta T, Oda M, Komure O, Udaka F, Kameyama M, Nakamura S, Kawakami H. Morino H, et al. Among authors: komure o. Ann Neurol. 2000 Apr;47(4):528-31. Ann Neurol. 2000. PMID: 10762168 Free article.

2

SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.

Izumi Y, Maruyama H, Oda M, Morino H, Okada T, Ito H, Sasaki I, Tanaka H, Komure O, Udaka F, Nakamura S, Kawakami H. Izumi Y, et al. Among authors: komure o. Am J Hum Genet. 2003 Mar;72(3):704-9. doi: 10.1086/367775. Epub 2003 Jan 21. Am J Hum Genet. 2003. PMID: 12545428 Free PMC article.

3

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H. Oda M, et al. Among authors: komure o. Arch Neurol. 2004 Feb;61(2):209-12. doi: 10.1001/archneur.61.2.209. Arch Neurol. 2004. PMID: 14967767

4

No association between apolipoprotein E alleles and olivopontocerebellar atrophy.

Toji H, Kawakami H, Kawarai T, Nakayama T, Komure O, Kuno S, Nakamura S. Toji H, et al. Among authors: komure o. J Neurol Sci. 1998 Jun 11;158(1):110-2. doi: 10.1016/s0022-510x(98)00099-9. J Neurol Sci. 1998. PMID: 9667788

5

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: komure o. Hum Mol Genet. 1997 Aug;6(8):1283-7. doi: 10.1093/hmg/6.8.1283. Hum Mol Genet. 1997. PMID: 9259274

6

Spinocerebellar ataxia type 6 in relation to CAG repeat length.

Kaseda Y, Kawakami H, Matsuyama Z, Kumagai R, Toji M, Komure O, Nishimura M, Izumi Y, Udaka F, Kameyama M, Nishio T, Sunohara N, Kuroda Y, Nakamura S. Kaseda Y, et al. Among authors: komure o. Acta Neurol Scand. 1999 Apr;99(4):209-12. doi: 10.1111/j.1600-0404.1999.tb07348.x. Acta Neurol Scand. 1999. PMID: 10225349

7

Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy.

Nishimura M, Kawakami H, Komure O, Maruyama H, Morino H, Izumi Y, Nakamura S, Kaji R, Kuno S. Nishimura M, et al. Among authors: komure o. Mov Disord. 2002 Jul;17(4):808-11. doi: 10.1002/mds.10124. Mov Disord. 2002. PMID: 12210881

8

Mutations of optineurin in amyotrophic lateral sclerosis.

Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H. Maruyama H, et al. Among authors: komure o. Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28. Nature. 2010. PMID: 20428114

9

C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8.

Kume K, Morino H, Komure O, Matsuda Y, Ohsawa R, Kurashige T, Kanaya Y, Tada Y, Kawakami H. Kume K, et al. Among authors: komure o. J Neurol Sci. 2019 Jul 15;402:118-120. doi: 10.1016/j.jns.2019.05.001. Epub 2019 May 9. J Neurol Sci. 2019. PMID: 31129264 No abstract available.

10

Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations.

Ayaki T, Ito H, Komure O, Kamada M, Nakamura M, Wate R, Kusaka H, Yamaguchi Y, Li F, Kawakami H, Urushitani M, Takahashi R. Ayaki T, et al. Among authors: komure o. J Neuropathol Exp Neurol. 2018 Feb 1;77(2):128-138. doi: 10.1093/jnen/nlx109. J Neuropathol Exp Neurol. 2018. PMID: 29272468

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