Sakoe K - Search Results

1

Middle cerebellar peduncles and Pontine T2 hypointensities in ARSACS.

Shimazaki H, Takiyama Y, Honda J, Sakoe K, Namekawa M, Tsugawa J, Tsuboi Y, Suzuki C, Baba M, Nakano I. Shimazaki H, et al. Among authors: sakoe k. J Neuroimaging. 2013 Jan;23(1):82-5. doi: 10.1111/j.1552-6569.2011.00647.x. Epub 2012 Jan 23. J Neuroimaging. 2013. PMID: 22268491

2

Identification of a SACS gene missense mutation in ARSACS.

Ogawa T, Takiyama Y, Sakoe K, Mori K, Namekawa M, Shimazaki H, Nakano I, Nishizawa M. Ogawa T, et al. Among authors: sakoe k. Neurology. 2004 Jan 13;62(1):107-9. doi: 10.1212/01.wnl.0000099371.14478.73. Neurology. 2004. PMID: 14718708

3

Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease.

Namekawa M, Takiyama Y, Aoki Y, Takayashiki N, Sakoe K, Shimazaki H, Taguchi T, Tanaka Y, Nishizawa M, Saito K, Matsubara Y, Nakano I. Namekawa M, et al. Among authors: sakoe k. Ann Neurol. 2002 Dec;52(6):779-85. doi: 10.1002/ana.10375. Ann Neurol. 2002. PMID: 12447932

4

An unusual case of a spasticity-lacking phenotype with a novel SACS mutation.

Shimazaki H, Sakoe K, Niijima K, Nakano I, Takiyama Y. Shimazaki H, et al. Among authors: sakoe k. J Neurol Sci. 2007 Apr 15;255(1-2):87-9. doi: 10.1016/j.jns.2007.02.002. Epub 2007 Mar 8. J Neurol Sci. 2007. PMID: 17349660

5

Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature.

Namekawa M, Takiyama Y, Honda J, Shimazaki H, Sakoe K, Nakano I. Namekawa M, et al. Among authors: sakoe k. BMC Neurol. 2010 Apr 1;10:21. doi: 10.1186/1471-2377-10-21. BMC Neurol. 2010. PMID: 20359319 Free PMC article. Review.

6

A novel adult case of juvenile-onset Alexander disease: complete remission of neurological symptoms for over 12 years, despite insidiously progressive cervicomedullary atrophy.

Namekawa M, Takiyama Y, Honda J, Sakoe K, Naoi T, Shimazaki H, Yamagata T, Momoi MY, Nakano I. Namekawa M, et al. Among authors: sakoe k. Neurol Sci. 2012 Dec;33(6):1389-92. doi: 10.1007/s10072-011-0902-z. Epub 2011 Dec 24. Neurol Sci. 2012. PMID: 22198646 Free PMC article.

7

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).

Shimazaki H, Takiyama Y, Ishiura H, Sakai C, Matsushima Y, Hatakeyama H, Honda J, Sakoe K, Naoi T, Namekawa M, Fukuda Y, Takahashi Y, Goto J, Tsuji S, Goto Y, Nakano I; Japan Spastic Paraplegia Research Consortium (JASPAC). Shimazaki H, et al. Among authors: sakoe k. J Med Genet. 2012 Dec;49(12):777-84. doi: 10.1136/jmedgenet-2012-101212. J Med Genet. 2012. PMID: 23188110

8

Machado-Joseph disease: cerebellar ataxia and autonomic dysfunction in a patient with the shortest known expanded allele (56 CAG repeat units) of the MJD1 gene.

Takiyama Y, Sakoe K, Nakano I, Nishizawa M. Takiyama Y, et al. Among authors: sakoe k. Neurology. 1997 Aug;49(2):604-6. doi: 10.1212/wnl.49.2.604. Neurology. 1997. PMID: 9270607

9

Choreiform movements in spinocerebellar ataxia type 1.

Namekawa M, Takiyama Y, Ando Y, Sakoe K, Muramatsu SI, Fujimoto KI, Nishizawa M, Nakano I. Namekawa M, et al. Among authors: sakoe k. J Neurol Sci. 2001 Jun 15;187(1-2):103-6. doi: 10.1016/s0022-510x(01)00527-5. J Neurol Sci. 2001. PMID: 11440752

10

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.

Shimazaki H, Takiyama Y, Sakoe K, Ikeguchi K, Niijima K, Kaneko J, Namekawa M, Ogawa T, Date H, Tsuji S, Nakano I, Nishizawa M. Shimazaki H, et al. Among authors: sakoe k. Neurology. 2002 Aug 27;59(4):590-5. doi: 10.1212/wnl.59.4.590. Neurology. 2002. PMID: 12196655

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