Namekawa M - Search Results

1

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: namekawa m. Neurology. 2002 Aug 27;59(4):590-5. doi: 10.1212/wnl.59.4.590. Neurology. 2002. PMID: 12196655

2

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. Ann Neurol. 2002 Dec;52(6):779-85. doi: 10.1002/ana.10375. Ann Neurol. 2002. PMID: 12447932

3

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. BMC Neurol. 2010 Apr 1;10:21. doi: 10.1186/1471-2377-10-21. BMC Neurol. 2010. PMID: 20359319 Free PMC article. Review.

4

A Japanese family with spinocerebellar ataxia type 6 which includes three individuals homozygous for an expanded CAG repeat in the SCA6/CACNL1A4 gene.

Takiyama Y, Sakoe K, Namekawa M, Soutome M, Esumi E, Ogawa T, Ishikawa K, Mizusawa H, Nakano I, Nishizawa M. Takiyama Y, et al. Among authors: namekawa m. J Neurol Sci. 1998 Jun 30;158(2):141-7. doi: 10.1016/s0022-510x(98)00108-7. J Neurol Sci. 1998. PMID: 9702684

5

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. 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

6

A Japanese SPG4 family with a novel missense mutation of the SPG4 gene: intrafamilial variability in age at onset and clinical severity.

Namekawa M, Takiyama Y, Sakoe K, Nagaki H, Shimazaki H, Yoshimura M, Ikeguchi K, Nakano I, Nishizawa M. Namekawa M, et al. Acta Neurol Scand. 2002 Dec;106(6):387-91. doi: 10.1034/j.1600-0404.2002.01254.x. Acta Neurol Scand. 2002. PMID: 12460147

7

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: namekawa m. Neurology. 2004 Jan 13;62(1):107-9. doi: 10.1212/01.wnl.0000099371.14478.73. Neurology. 2004. PMID: 14718708

8

[Japan spastic paraplegia research consortium (JASPAC)].

Takiyama Y, Ishiura H, Shimazaki H, Namekawa M, Takahashi Y, Goto J, Tsuji S, Nishizawa M. Takiyama Y, et al. Among authors: namekawa m. Rinsho Shinkeigaku. 2010 Nov;50(11):931-4. doi: 10.5692/clinicalneurol.50.931. Rinsho Shinkeigaku. 2010. PMID: 21921516 Japanese.

9

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. 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.

10

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: namekawa m. 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

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